The heat soared to record temps of 100 degrees. I stood on my shoreline looking out towards the small island. The lake seemed void of any life. Not even the ducks were out swimming now. The water felt almost as warm as a drawn bath and the soft sand beneath me squished in be tween my toes. Standing in the water felt good and somewhat cooler than the thick July air. I wanted desperately to enjoy some outdoor time with my sons, but the weather forecast for the next few days showed no signs of the scorching temperatures dropping. The humid air weighed heavy, with an almost suffocating feeling as I breathed in.
Standing next to my new dock I watched as some minnows swam past me. We had made so many changes in the past two years it was a relief to actually feel I could sit back and enjoy some leisure time like sitting by the water. Last summers flooding had prevented us from making the necessary adaptions to my dock that would accommodate my sons electric wheelchairs. Now that it is was finally finished, this year we faced dangerous heat levels. I looked over at the new wide platform extending out into the water that we had designed for Josiah and Cody, recalling this past spring when I invited both my sons classmates out to our home. I felt happy that both boys were able to have had the opportunity to open up their private world to their peers. We had worked so hard at making the dock accessible and safe for the boys. Not only had we doubled the width but also added a raised lip along the sides to ensure the wheelchairs would not roll off. The entrance to the dock was leveled to allow full accessibility and recently rod holders had been installed at the deep end of the of the dock allowing my sons to enjoy fishing with minimal assistance. It pleased me so much that I had been able to find away to sort of lessen the limitations that DMD continually created.
In spite of the heat I felt a calm and peacefulness fill me, as I looked back out over the water. In so many ways I knew we all felt more at home here. Yes, this heat I knew would soon pass and once again the boys would enjoy fishing off the dock and trips to the beach. It was only days ago when from inside the house I could hear laughter from my niece Kayla and Josiah as they played together. Watching from our large window that overlooked the lake, I could see Kayla, my ten year old niece assisting Josiah as he reeled in a small sunfish. I was amazed at her ability to assist him with so much patience and love at such a young age. It was so heart warming for me to see Josiah in pure joy with his cousin. Again, over and over she baited his hook and cast out his line. They would both giggle as very diligently he pulled in the baby sunfish that would attach itself to his hook. Kayla encouraging him to do as much as possible himself reeling in the fish, where, she would immediately be waiting and ready to release his catch back into the lake. Laughing and smiling together they fished. After watching for a few minutes. I had decided to approach them with a tray of assorted snacks and drinks. I was even more pleased to learn that she had even taken it upon herself to apply sun screen on the bare parts of his exposed flesh. Absolutely, we were blessed to be able to share our world with family that gave back so willingly of themselves
Today though I was concerned, we would again be confide indoors. I pulled my cell phone from my pocket and glanced at the time, the boys would becoming home from their summer jobs shortly. A county program I was so fortunate to learn about. Both boys had been accepted into this project that employed disabled youth and young adults. The school district supplied the accessible bus that picked them up from home each morning and dropped them off each afternoon. I was so happy they both liked the experience and could already see how much it did for their self esteem and social skills. Four days a week for 5 weeks during the summer, my little guys would spend four hours in the morning doing various task and earn paychecks. Something I thought might not ever have been possible.
I walked along the shoreline enjoying my last few free minutes before I went to the front yard to wait for the bus. In spite of the current heat, the summer seemed to be going very well for us. I was satisfied with what I was accomplishing as a parent and so happy to see my sons thriving. I began walking to the house. Now out of the water I felt the intensity of the heat even more. I was looking forward to going inside our cool air conditioned home, where I knew there was plenty to keep my sons entertained. We had gaming systems, Legos and the computer, and we still had the rest of summer to spend outdoors.
It was my niece Kayla who was the answer to helping my boys discover fun did not have to involve electronics. The joy she brought into Josiah and Cody's world moved me so deeply. Their limitations never seemed to stop her from discovering new ways to get them to explore the world, outside thier comfort zone. So here it was, with the extreme temps rising to very uncomfortable levels we would be forced to spend several days in doors . With Kayla joining us I had no doubt it would include fun.
Kayla joined us shortly after we had finished lunch. With her came her beautiful enthusiasm and nurturing care she generously offered out to her challenged cousins. It seemed only moments after her father dropped her off she was running down the hall towards my sons Lego room to engage in play with them. Only moments later, she came back pushing Josiah, telling me they all were going to play school. Parking him comfortably in front an activity table, that I had made accessible for them in our large great room, she was off again, this time to help assist Cody. Surprising us both, Cody had taken it upon himself to join Kayla and Josiah. Amazingly, Kayla and I watched, as Cody pushed himself along with his legs while sitting in his desk chair. Purposely I have both my sons use leather high back desk chairs on wheels while in their Lego room. My hopes are to encourage them as long as possible to use any amount of muscle strength they might still maintain. His feet squarely planted on the floor he inched his way forward. Smiling he looked up to where I stood next to Kayla telling me "see I can do it myself mom". I felt so much admiration for him and what he was actually achieving. "Yes you are " I said as I looked at my almost 19 year old Cody, feeling so proud of him. I am not sure if Cody even knows how amazing what he was accomplishing was. I was thrilled, he made it all the way across our house by using his legs and feet to propel himself backwards
I was cleaning up the lunch dishes listening to sweet sounds of laughter escape from the three of them as they played. Curious I had to ask who was the teacher of the classroom that consisted of stuff animals collectively scattered on different chairs with name cards neatly taped to the edges. Kala immediately told me she was the teacher, Josiah chimed in" that he was the principal". Cody remarked loudly " because Josiah is so bossy he has to be the principal." This had become so true in the last year. Some how my quiet little Josiah had out grown his timidness and developed a talent to be bossy. "Cody" I asked "and what role do you play?" Smiling he said he was the janitor. Followed by " I need a mop please". I was delighted, I had someone to help clean the house. Anxious, to see what he might do I arranged a swiffer wet mop for him. The light handle drip less mop I thought might be somewhat easy for him to maneuver. Happily he scooted around pushing his mop. What could be better I thought, my children at play and actually exercising too. Moving about, using muscles and feeling proud and I was benefiting by having my floors cleaned. Several minutes later Cody stopped cleaning. He had noticed a spot ton the floor that was not easily coming clean. He asked me to get him a wipey. I obliged bringing him the cloth. I was not really paying much attention to his intended use until I noticed Cody struggled momentarily trying to reach the hardwood floor with his hand. Leaning forward he stretched out his arm, still he was to short to reach the spot that captivated him at the moment. I watched waiting for a cue from him for me to offer assistance. Slowly, my brilliant son dropped the cloth to the floor at his side, he then turned himself and the chair so that his feet faced the cloth. Almost as though he was calculating his next move he lifted his foot and placed it on top of the moist towel. Smiling he looked up to me and told me he needed to rub the spot harder. I felt a tear form in my eye as I watched in utter amazement, slowly and steadily his leg moved sliding his foot back forth with the fabric underneath. This was my son, determined and confident. We all praised Cody for his success. When I reached down after Cody had finished cleaning the soiled spot was gone, the wipe now held the dirt. Cody had indeed accomplished the task he set out for. Loudly he let us all know that is why he is the janitor.
It is in these moments that I am reminded of the special gifts I am blessed with. Blessed because through my children I can see beauty in something so insignificant to the outer world. Blessed because if nothing else other than feeling loved I have helped my sons become determined spirits, thriving and believing in themselves. While I will still have days of despair and fear will seem to at times invade the depths of my being as I watch this disease attack my sons without mercy, when I choose to look beyond, I will be given a glimmer of light, that will fill me with strength to face whatever challenge may lay ahead with determination and hope.
Thursday, July 5, 2012
Tuesday, July 3, 2012
Slowly I backed my van toward the single cement step leading up to my front door. This appeared to be the easiest way for me to load Josiah and Cody's motorized wheelchairs into the rear end of my navy blue Dodge Caravan. I knew I would still have to use our clunky awkward but dependable, steal portable suitcase ramp to drive the chairs across on entry. However, I felt somewhat relaxed with the low incline- from going step to van, and bridging with the ramp. A welcome relief for my fear, that should I slip the chairs would not roll back and trap me, as it had happened in the past. Glancing into the van I paused momentarily scanning the space available for me to haul the cumbersome equipment we now needed. I peered back to the front door where Josiah's chair waited for me. I again, sized the chair up form side to side. Yes, I knew what I had to do, and felt determined. After all I had been tackling loading equipment by myself for many years. However, as my boys have grown, so has their needs and size of wheelchairs. Unhappy with my limited choices, today I had decided on a different approach.
I paused thinking about the weeks earlier disappointments, my purchasing a gate trailer and hitch that I wanted to use to haul one wheelchair outside the van, allowing me more space inside to seat passengers while only having to load one chair in the vehicle. I had hoped my new scooter/wheelchair carrier would aide in my transporting the boys and their motorized equipment. I envisioned this would add new convenience into our limited world, giving me some major ease with the transportation choices for my sons. Sadly my latest attempt to find an affordable new spacious approach failed. Miserably I added the defeat to an already growing list for the week. Now not only did I have to recover from a several thousand dollar wage loss but I also owned very expensive beach chairs that were not owning up to its claim of ease. This new large metal rack now broke what had already weakened my spirit. So as it were I felt obstacles and stumbling blocks surround me. Leaving me amidst all my errors and set backs, left only to find new ways to set forth on a path to rise above my present demise.
Propping open my front door, I momentarily recalled how on previous trips, I had always resorted to lowering one of the stow and go middle passenger seats into its storage compartment in the vans floor. Giving me the very much needed space to load our 2 electric chairs, a ramp along with what ever else we would need for our adventure. Unfortunately though it never left us much room to allow us to have an adult size passenger ride along. The only area left to spare was a small split section of the very rear stow and go seat, with scarcely enough leg and foot space for a child, or small accommodating adult, such as my self. Desperately to day, the day of my niece Vanessa's wedding reception, I wanted to keep the left mid passenger seat in tact.
I had spent time researching and planning for this day, to find a way that allowed me the comfort to be seated with out having to crawl to the rear of my van, in my dress and heels. I wanted to have room and just this once be honored with the pleasure of an escort accompany us for our special night. My male companion for the evening was Craig. A very close friend whom I had been seeing and recently begun joining my boys and I on occasion to events. Standing at six foot three with very broad shoulders, it was very apparent, there would be no possible way to seat him in the rear, surrounded by equipment. With Cody and Josiah occupying their tourney seats there would be no other seat available to accommodate his size. He would have to sit in the drivers seat. I knew I had to try and find another way to load my cargo, or resort to crawling in the back, with gown and heels.
I thought about the tears I had cried earlier in the week from letting my hope build, and be left with yet another let down. Tears that grew out of fear from me failing at my attempt to become more independent with my sons and their ever increasing needs. Most importantly, tears because in so many ways this only increased the isolation and imprisonment I see ahead for them -for me -for us. Sadly, I just did not even begin to know where to turn too, to share my sorrow with out feeling I was being seen as a drama queen, or be showered with useless advice. I felt bad, and just wanted to have some where or someone to vent. With the reality that staff, family and friends are not always available, I felt an even more urgency to address the situation on my own, to keep from hearing again, the before mention label-Drama queen. Somehow I found the words still stung at me, while I scanned the door frame size one last time to my house. An uneasiness stirred in me, as I thought about what I desired most. Was it physical support, or just some real heartfelt emotional support, that would let me keep my dignity and not be judged. I had read a posting on Face book a few days ago where a friend had posted she was having a bad day. She was so thankful and delighted when a close friend appeared at her door unannounced with a bottle of wine. I imagined as I read the posting, how special and loved she must have felt. I was delighted for her- but found myself wishing I had that in my life right now. Just once, I wanted affection without having to ask for it.
It wasn't the money and time spent researching that left me so upset, it wasn't even the fact that I now owned items that were not living up to my expectations or needs they were unable to meet and failed. But, solely the acceptance that once again DMD had appeared to have control over another aspect of my world -the world that my two sons and I live in. So, here I was recovering from a week of feeling like I failed in many choices lately, and at a loss, to find away to provide more accessibility for my sons. How many set backs can one week bring? I wondered, as I began to set up the rigid ramp. With no tears left, and a bit angered at myself for falling victim to self pity, I now felt determined to tackle my current dilemma. So far, no answer to our situation had been rendered that would improve my being faced with unloading these chairs at a very steep incline by myself, at some point, and most likely often. I shifted the heavy metal ramp and thought about the set back the current situation produced. Reality stung at me, single parenting slapping me in the face. Faced with- short staff and short funds I had to be everything and find ways to do it all. This was our life like it or not, I carried the load to our survival, our thriving.
Letting my thoughts carry me away, I wondered what was it even like to be a parent, and go somewhere with out having to put so much thought, planning and preparation into it. Unfortunately needs and emergencies arise often at the most inopportune times. Could I really have my sons transportation exist at the mercy of others? Hope that help would be available when I needed. Would that be acceptable for the bazillion of other parents I knew? Would they really accept living that way, of course not. I tried to imagine if I personally knew anyone, who really understood the stress and fear, of being in that situation. A situation, I knew to well. A problem I wanted to avoid ever happening again.
I began to disassemble as many removable parts as possible on both chairs. The backs with headrest and then foot rest. Carefully, with Josiah's chair on a very low speed I slowly backed it in the van. After several attempts I had it backed as close as possible to the passenger seat on the left side of the van. Cody's chair was next. All I could do was try, at the very worst I would be sandwiched in between the chairs for the ride, if my idea failed. With extreme caution and persistence, some clanking of wheels colliding from one chair to the next, it appeared I had made a successful fit, barely but it worked. I was successful. My first thought was take that DMD.
Half amazed that by myself, I had actually attempted something that no else that had offered me help had thought of. I surveyed my solution. Empowered I stepped inside the van to take a different look, just to ensure I had not forgot something. Yes, I had managed to fit it all. Even though it required removing the chairs of some hardware, it all fit. I finished placing the ramp and the other parts I had stripped from the chairs in my van. I smiled as I heard the rear gate door close with out so much as a ting. I was done and now had time to spend getting myself ready.
The wedding reception was wonderful. My sons enjoyed themselves and their freedom to roam. I found an inner peace with in myself that night. I felt joy that I was able to be more when I had too, once again.
I did manage to impress Craig and my brother-in law Bill some, with my talent to fit the wheelchairs side by side on my own, something, neither had thought of. However, I know in reality it only helped both feel assured, I had moved on and as usual made things workout. I, on the other hand had assured myself how very important every step I take towards my sons care must be. Most importantly, there is no end to learning on this journey and the level of commitment I need.
I may not ever know the comfort that comes with having someone to share your innermost fears and pain with. I do not ever expect anyone outside the DMD community to begin to understand the magnitude of emotions we struggle with daily, or the the strength it takes as parents of children who are born with an expiration date. Those are things I have no more control over than the progressing muscle loss my sons continue to endure. I do know, I at times need to be so much more, and hope for so much more. From time to time I will fail, and the ones that are around me offering support may fail. I can move past all that and grow. With dignity and pride, I will pull myself up to continue to discover the things I am capable of, through my perseverance and unconditional love for my sons. With out hesitation, I can tell you I am a DMD mother first and that is my whole world, where ever I go and what ever I am doing.
I paused thinking about the weeks earlier disappointments, my purchasing a gate trailer and hitch that I wanted to use to haul one wheelchair outside the van, allowing me more space inside to seat passengers while only having to load one chair in the vehicle. I had hoped my new scooter/wheelchair carrier would aide in my transporting the boys and their motorized equipment. I envisioned this would add new convenience into our limited world, giving me some major ease with the transportation choices for my sons. Sadly my latest attempt to find an affordable new spacious approach failed. Miserably I added the defeat to an already growing list for the week. Now not only did I have to recover from a several thousand dollar wage loss but I also owned very expensive beach chairs that were not owning up to its claim of ease. This new large metal rack now broke what had already weakened my spirit. So as it were I felt obstacles and stumbling blocks surround me. Leaving me amidst all my errors and set backs, left only to find new ways to set forth on a path to rise above my present demise.
Propping open my front door, I momentarily recalled how on previous trips, I had always resorted to lowering one of the stow and go middle passenger seats into its storage compartment in the vans floor. Giving me the very much needed space to load our 2 electric chairs, a ramp along with what ever else we would need for our adventure. Unfortunately though it never left us much room to allow us to have an adult size passenger ride along. The only area left to spare was a small split section of the very rear stow and go seat, with scarcely enough leg and foot space for a child, or small accommodating adult, such as my self. Desperately to day, the day of my niece Vanessa's wedding reception, I wanted to keep the left mid passenger seat in tact.
I had spent time researching and planning for this day, to find a way that allowed me the comfort to be seated with out having to crawl to the rear of my van, in my dress and heels. I wanted to have room and just this once be honored with the pleasure of an escort accompany us for our special night. My male companion for the evening was Craig. A very close friend whom I had been seeing and recently begun joining my boys and I on occasion to events. Standing at six foot three with very broad shoulders, it was very apparent, there would be no possible way to seat him in the rear, surrounded by equipment. With Cody and Josiah occupying their tourney seats there would be no other seat available to accommodate his size. He would have to sit in the drivers seat. I knew I had to try and find another way to load my cargo, or resort to crawling in the back, with gown and heels.
I thought about the tears I had cried earlier in the week from letting my hope build, and be left with yet another let down. Tears that grew out of fear from me failing at my attempt to become more independent with my sons and their ever increasing needs. Most importantly, tears because in so many ways this only increased the isolation and imprisonment I see ahead for them -for me -for us. Sadly, I just did not even begin to know where to turn too, to share my sorrow with out feeling I was being seen as a drama queen, or be showered with useless advice. I felt bad, and just wanted to have some where or someone to vent. With the reality that staff, family and friends are not always available, I felt an even more urgency to address the situation on my own, to keep from hearing again, the before mention label-Drama queen. Somehow I found the words still stung at me, while I scanned the door frame size one last time to my house. An uneasiness stirred in me, as I thought about what I desired most. Was it physical support, or just some real heartfelt emotional support, that would let me keep my dignity and not be judged. I had read a posting on Face book a few days ago where a friend had posted she was having a bad day. She was so thankful and delighted when a close friend appeared at her door unannounced with a bottle of wine. I imagined as I read the posting, how special and loved she must have felt. I was delighted for her- but found myself wishing I had that in my life right now. Just once, I wanted affection without having to ask for it.
It wasn't the money and time spent researching that left me so upset, it wasn't even the fact that I now owned items that were not living up to my expectations or needs they were unable to meet and failed. But, solely the acceptance that once again DMD had appeared to have control over another aspect of my world -the world that my two sons and I live in. So, here I was recovering from a week of feeling like I failed in many choices lately, and at a loss, to find away to provide more accessibility for my sons. How many set backs can one week bring? I wondered, as I began to set up the rigid ramp. With no tears left, and a bit angered at myself for falling victim to self pity, I now felt determined to tackle my current dilemma. So far, no answer to our situation had been rendered that would improve my being faced with unloading these chairs at a very steep incline by myself, at some point, and most likely often. I shifted the heavy metal ramp and thought about the set back the current situation produced. Reality stung at me, single parenting slapping me in the face. Faced with- short staff and short funds I had to be everything and find ways to do it all. This was our life like it or not, I carried the load to our survival, our thriving.
Letting my thoughts carry me away, I wondered what was it even like to be a parent, and go somewhere with out having to put so much thought, planning and preparation into it. Unfortunately needs and emergencies arise often at the most inopportune times. Could I really have my sons transportation exist at the mercy of others? Hope that help would be available when I needed. Would that be acceptable for the bazillion of other parents I knew? Would they really accept living that way, of course not. I tried to imagine if I personally knew anyone, who really understood the stress and fear, of being in that situation. A situation, I knew to well. A problem I wanted to avoid ever happening again.
I began to disassemble as many removable parts as possible on both chairs. The backs with headrest and then foot rest. Carefully, with Josiah's chair on a very low speed I slowly backed it in the van. After several attempts I had it backed as close as possible to the passenger seat on the left side of the van. Cody's chair was next. All I could do was try, at the very worst I would be sandwiched in between the chairs for the ride, if my idea failed. With extreme caution and persistence, some clanking of wheels colliding from one chair to the next, it appeared I had made a successful fit, barely but it worked. I was successful. My first thought was take that DMD.
Half amazed that by myself, I had actually attempted something that no else that had offered me help had thought of. I surveyed my solution. Empowered I stepped inside the van to take a different look, just to ensure I had not forgot something. Yes, I had managed to fit it all. Even though it required removing the chairs of some hardware, it all fit. I finished placing the ramp and the other parts I had stripped from the chairs in my van. I smiled as I heard the rear gate door close with out so much as a ting. I was done and now had time to spend getting myself ready.
The wedding reception was wonderful. My sons enjoyed themselves and their freedom to roam. I found an inner peace with in myself that night. I felt joy that I was able to be more when I had too, once again.
I did manage to impress Craig and my brother-in law Bill some, with my talent to fit the wheelchairs side by side on my own, something, neither had thought of. However, I know in reality it only helped both feel assured, I had moved on and as usual made things workout. I, on the other hand had assured myself how very important every step I take towards my sons care must be. Most importantly, there is no end to learning on this journey and the level of commitment I need.
I may not ever know the comfort that comes with having someone to share your innermost fears and pain with. I do not ever expect anyone outside the DMD community to begin to understand the magnitude of emotions we struggle with daily, or the the strength it takes as parents of children who are born with an expiration date. Those are things I have no more control over than the progressing muscle loss my sons continue to endure. I do know, I at times need to be so much more, and hope for so much more. From time to time I will fail, and the ones that are around me offering support may fail. I can move past all that and grow. With dignity and pride, I will pull myself up to continue to discover the things I am capable of, through my perseverance and unconditional love for my sons. With out hesitation, I can tell you I am a DMD mother first and that is my whole world, where ever I go and what ever I am doing.
Saturday, June 16, 2012
for keeps sake....
His beautiful brown eyes looked deeply into mine. Quietly he waited for my response. I understood the apprehension he was feeling at the moment. Quite frankly every other weekend I experience similar uneasiness as I send my sons off to their fathers for the weekend. While I know my sons father loves them, there is most definitely concern in the quality of care he provides. Especially knowing their apprehensiveness to alert him if he has not met all their needs. In my heart I knew this night tonight was a step forward for us all. A step I needed to make to ensure we were all moving in the right direction.
Gently I gave my little Josiah a squeeze as I kissed him on the forehead. "This will be a fun guys night" I said, desperately hoping, I could help him move past his uncomfortableness before he embarked on his evening out. "I am not sure about this mom. You know how to lift me better than anyone." His voice cracked with adolescence, as he spoke. My last born was slowly turning into a young man right before my eyes. I smiled as I looked at his gentle face admiring his youth. Stepping aside to allow him room to grow was not easy for me. My own anxiety of separation softly whispered to me. I secretly did not want to let go of his dependence on me any more than he did. But I knew we both had to move forward. For the past seven years I had been the only consistent immediate role model for all three of my sons. Sharing our world with anyone that did not live up to my expectations just was not acceptable at any cost. Now with these tender teen years in full bloom I wanted\ Josiah to enjoy more positive male bonding time. Preferable with a man that held positive endearments toward me. Someone that respected my authority with out challenge. Most importantly some one who did not feel burdened and that would embrace the challenges of caring for a child with special needs.
I knew he still was not totally convinced he and his brother would survive the evening with out my presence, to supervise their care. I on the other hand felt total comfort in the decision to have my sons enjoy an evening out, without me. A guys night, that also still included a family member. Their loving uncle Bill would also be joining them for the evening. I felt confident between these two wonderful men my boys would not only enjoy themselves but, be very safe and well cared for. It was time Josiah allowed another caring human in to his comfort zone with out my constant presence. I just needed to assure him. I wanted desperately to explore the opportunity for them to develop a new friendships. To see them engage in outings out in the community, trusting that they could survive being in the care of someone other than me, or my sister and her husband.
Helping Josiah to advocate his needs more has been challenging for both of us. At times even disheartening for me knowing that he can become so uncomfortable in new surroundings he will not ask for help when he needs it.
We talked some more about doing things with out mom. Me reminding him he goes on field trips at school with just his class and teacher. That he and his brother stay at home alone with our sitter who is not related. Most importantly we talked about making new friends. Smiling at me, he finally said he would be fine at the races without me. But he would miss me very much. He appeared to be even more comfortable with the idea, when I asked him to be the teacher and help Craig learn how to care for him and his brother Cody. After packing my boys in the car and going over a verbal list of do and don'ts with my sons, some hugs and kisses, they left for guys night out at the car race track. I was assured through a couple of texts and a phone call the evening was going very well. The smiles my men had when they arrived home assured me, yes everything went well, very well.
As a single parent I have now reached another milestone in the DMD world. I have taken a step forward in opening a door allowing more opportunities for my sons to grow beyond my ties to them. Most importantly I have found the courage to entrust my beautiful sons care into the hands of someone I care very deeply for.
Opening our lives to something new can often be scary and exciting. When I put my sons to bed that night I asked them teasing if we should keep Craig. Cody told me excitedly "Yes we should, because Craig is a good man". He repeated several times to me, Craig is a good man, mom. Josiah called me near him to whisper, "we should keep him, but next time we should all go to the races together." Laughing I asked him why? " I thought you had fun with just the guys". Giggling he said " I like seeing you and Craig together mom, its funny when you kiss. We can keep him, but you have the next date alone." " I like that plan." I said as I kissed them both good night.
Gently I gave my little Josiah a squeeze as I kissed him on the forehead. "This will be a fun guys night" I said, desperately hoping, I could help him move past his uncomfortableness before he embarked on his evening out. "I am not sure about this mom. You know how to lift me better than anyone." His voice cracked with adolescence, as he spoke. My last born was slowly turning into a young man right before my eyes. I smiled as I looked at his gentle face admiring his youth. Stepping aside to allow him room to grow was not easy for me. My own anxiety of separation softly whispered to me. I secretly did not want to let go of his dependence on me any more than he did. But I knew we both had to move forward. For the past seven years I had been the only consistent immediate role model for all three of my sons. Sharing our world with anyone that did not live up to my expectations just was not acceptable at any cost. Now with these tender teen years in full bloom I wanted
I knew he still was not totally convinced he and his brother would survive the evening with out my presence, to supervise their care. I on the other hand felt total comfort in the decision to have my sons enjoy an evening out, without me. A guys night, that also still included a family member. Their loving uncle Bill would also be joining them for the evening. I felt confident between these two wonderful men my boys would not only enjoy themselves but, be very safe and well cared for. It was time Josiah allowed another caring human in to his comfort zone with out my constant presence. I just needed to assure him. I wanted desperately to explore the opportunity for them to develop a new friendships. To see them engage in outings out in the community, trusting that they could survive being in the care of someone other than me, or my sister and her husband.
Helping Josiah to advocate his needs more has been challenging for both of us. At times even disheartening for me knowing that he can become so uncomfortable in new surroundings he will not ask for help when he needs it.
We talked some more about doing things with out mom. Me reminding him he goes on field trips at school with just his class and teacher. That he and his brother stay at home alone with our sitter who is not related. Most importantly we talked about making new friends. Smiling at me, he finally said he would be fine at the races without me. But he would miss me very much. He appeared to be even more comfortable with the idea, when I asked him to be the teacher and help Craig learn how to care for him and his brother Cody. After packing my boys in the car and going over a verbal list of do and don'ts with my sons, some hugs and kisses, they left for guys night out at the car race track. I was assured through a couple of texts and a phone call the evening was going very well. The smiles my men had when they arrived home assured me, yes everything went well, very well.
As a single parent I have now reached another milestone in the DMD world. I have taken a step forward in opening a door allowing more opportunities for my sons to grow beyond my ties to them. Most importantly I have found the courage to entrust my beautiful sons care into the hands of someone I care very deeply for.
Opening our lives to something new can often be scary and exciting. When I put my sons to bed that night I asked them teasing if we should keep Craig. Cody told me excitedly "Yes we should, because Craig is a good man". He repeated several times to me, Craig is a good man, mom. Josiah called me near him to whisper, "we should keep him, but next time we should all go to the races together." Laughing I asked him why? " I thought you had fun with just the guys". Giggling he said " I like seeing you and Craig together mom, its funny when you kiss. We can keep him, but you have the next date alone." " I like that plan." I said as I kissed them both good night.
Wednesday, May 2, 2012
a bump in the dark
I heard the calls to me from in between weakened coughs, I knew I had to get to Cody fast. I shook my head to escape the daze feeling that was beginning to invade me. I just had no time right now to deal with another crisis. Beneath my fingers I could already feel a lump under my eye brow growing and the pain increasing. I wanted to cry out, I hurt, but I would only frighten my sons and have even more to take care of. In the dim light I headed towards Cody, careful not to wake his brother Josiah who I could hear breathing softly across the room. At least there seemed to be no wetness coming form my head, as I gently touched the bump resembling a little bit of an eye brow. I felt somewhat relieved that I had not broken any skin. My impact with the door might not be as bad as it was feeling.
I helped Cody to sit up in hopes it would help him produce a working cough faster. I fumbled around at his bedside to locate his remote control to raise the head of his bed up, while I cradled his head in one arm. He felt warm, his fever had come back and he was now even more congested. As his bed rose I also could see he would need repositioning. What made matters worse I could also now see a shadow appearing over the top of my eye ball. For a second it frightened me as I thought about trying to drive Cody to the emergency room with one eye swollen shut.
I needed an ice pack fast and Cody needed me right now to help him work through his coughing spell. Of course I could wait. It is those moments when somewhere from with in you just know instinctively how to stay calm and manage. As if on cue Cody released some phlegm and began to relax alittle. He appeared to not be in any real distress for the moment, giving me seconds to quickly run to find the ice pack I would be spending the next few hours with.
After getting him comfortably back in bed, re medicated and assuring him my head was fine, I tiptoed from his room down the hall to the guest bathroom. I now had time to take a glance in the mirror at the damage. Yes, I would undoubtedly have a black eye forming by morning. However, night was not over, I would need to combat pain and fatigue if he should call to me again. Images of me out from a concussion flashed through my mind. What if I was not alert enough to even help my son. Already sleep deprived there just was not much else I could do. I had to stay close by him, it pained me to see him struggle so hard. I curled up in the recliner across from his bed with the ice pack over my eye, praying for peaceful sleep for the both of us.
I helped Cody to sit up in hopes it would help him produce a working cough faster. I fumbled around at his bedside to locate his remote control to raise the head of his bed up, while I cradled his head in one arm. He felt warm, his fever had come back and he was now even more congested. As his bed rose I also could see he would need repositioning. What made matters worse I could also now see a shadow appearing over the top of my eye ball. For a second it frightened me as I thought about trying to drive Cody to the emergency room with one eye swollen shut.
I needed an ice pack fast and Cody needed me right now to help him work through his coughing spell. Of course I could wait. It is those moments when somewhere from with in you just know instinctively how to stay calm and manage. As if on cue Cody released some phlegm and began to relax alittle. He appeared to not be in any real distress for the moment, giving me seconds to quickly run to find the ice pack I would be spending the next few hours with.
After getting him comfortably back in bed, re medicated and assuring him my head was fine, I tiptoed from his room down the hall to the guest bathroom. I now had time to take a glance in the mirror at the damage. Yes, I would undoubtedly have a black eye forming by morning. However, night was not over, I would need to combat pain and fatigue if he should call to me again. Images of me out from a concussion flashed through my mind. What if I was not alert enough to even help my son. Already sleep deprived there just was not much else I could do. I had to stay close by him, it pained me to see him struggle so hard. I curled up in the recliner across from his bed with the ice pack over my eye, praying for peaceful sleep for the both of us.
Thursday, April 12, 2012
I stood in the black glittery almost stiletto heels staring at my self in the full length mirror. My legs appeared a bit longer and more slender. Yes, the shoes my younger sister Roxanne had left behind, when she came to visit for Easter did help me feel sexier, maybe even a bit younger. I loved the sparkle, the shape and the height it gave me. I smiled, admiring the way my calves appeared to have lengthened. I followed my reflection, stepping back as I turned slightly to catch a side glimpse. They were deffinetely very glamorous shoes. Shoes that were me, perhaps some 20 years ago. Shoes, that I would have danced the night away in and not given the heel height a second thought, years ago. Shoes, that even though were my size, no longer fit in my life. Shoes that belonged in my younger sisters life style.
Carefully I stepped out of the high heels and planted my feet squarely back on the hard wood floor. Twirling in my new dress I headed back down the hall to my bedroom. Waiting for me in my closet were a lovely pair of sensible strappy sandals in black patent. I slid my feet in them and stepped back out in to the hall to critique my image. My freshly painted pink toenails matched the hot pink trim in my dress perfectly. While the heals were some what lower, I was very pleased. My feet I decided looked pretty with a sleek sexy bareness about them. Without anymore hesitation I knew my outfit was now complete and I was ready for the prom dance I had been invited to with my two younger sons the coming weekend.
My sister Marie and I had busily spent the early part of the week shortening our formal gowns to just above the knee. Having been unable to find dresses that created the elegance we wanted in shorter lengths we opted to design our own versions. By altering the hems lines of some off the rack prom dresses we had found we were able to create gowns that allowed us the capability to move freely. Accompanying my sons Cody and Josiah to prom was such an honor, we both looked forward too. Even though this night was a formal affair we would still have to be caretakers and lift and maneuver my sons through out the evening. Dressing for the occasion had such a deep meaning to us.
I smiled to myself recalling last years Shriners Prom. We had just gotten to the dance, I was helping to get Cody out of my van and stepped on the hem of my dress, while adjusting him in his chair. Only able to find one safety pin, I tried desperately to create a neat gathering of fabric in the front of my ruby red gown and spent the rest of night trying to keep from stressing the satin material. By the end of the night I had ripped my dress down in a several places. I had decided then and there on that night, I would never again choose to wear a gown to the floor. Keeping in mind however to short poses a problem with lifting too. Strapless dresses are also not on my to wear list when I am in my caretaker mode. I am some how unable to lift bodies and keep my top in place. A lesson also learnt the hard way.
With my sons almost magically coordinated with our backless gowns we seem to be ready. Using the left over fabric from shortening our dresses Marie created bow ties and a cumberbun for Josiah to match. I will have to admit however I did have to really talk my both my sons into agreeing to wear the pink bow ties that had been designed for them. Now with their suits pressed we are all looking so forward to this wonderful evening.
While I anxiously await this special evening with my sons I cannot help but think about changes. Not only changes age has made on me but changes the life I am called to live requires of me. My life with Duchenne at times demands of me to surrender and adapt to changes. Changes that I am not always eager to embrace or accept. The effect that this disease has had on my life is so great that even my fashion style has been effected. I will always admire the glittery, and delicate clothing I once could adorn freely. It will always be in me to secretly want to bare my shoulders or cover myself in sequence. The shoes I buy now will have a somewhat lower modest heel to help me stay balanced when lifting more than my weight. On occasion I hope to still attend events that will allow me the opportunity to borrow a few accessories from my younger sisters more youthful wardrobe. I will however let her keep the stilettos on her feet and accept that I must be a bit more grounded and at times even more modest to meet the tender needs of my sons.
Carefully I stepped out of the high heels and planted my feet squarely back on the hard wood floor. Twirling in my new dress I headed back down the hall to my bedroom. Waiting for me in my closet were a lovely pair of sensible strappy sandals in black patent. I slid my feet in them and stepped back out in to the hall to critique my image. My freshly painted pink toenails matched the hot pink trim in my dress perfectly. While the heals were some what lower, I was very pleased. My feet I decided looked pretty with a sleek sexy bareness about them. Without anymore hesitation I knew my outfit was now complete and I was ready for the prom dance I had been invited to with my two younger sons the coming weekend.
My sister Marie and I had busily spent the early part of the week shortening our formal gowns to just above the knee. Having been unable to find dresses that created the elegance we wanted in shorter lengths we opted to design our own versions. By altering the hems lines of some off the rack prom dresses we had found we were able to create gowns that allowed us the capability to move freely. Accompanying my sons Cody and Josiah to prom was such an honor, we both looked forward too. Even though this night was a formal affair we would still have to be caretakers and lift and maneuver my sons through out the evening. Dressing for the occasion had such a deep meaning to us.
I smiled to myself recalling last years Shriners Prom. We had just gotten to the dance, I was helping to get Cody out of my van and stepped on the hem of my dress, while adjusting him in his chair. Only able to find one safety pin, I tried desperately to create a neat gathering of fabric in the front of my ruby red gown and spent the rest of night trying to keep from stressing the satin material. By the end of the night I had ripped my dress down in a several places. I had decided then and there on that night, I would never again choose to wear a gown to the floor. Keeping in mind however to short poses a problem with lifting too. Strapless dresses are also not on my to wear list when I am in my caretaker mode. I am some how unable to lift bodies and keep my top in place. A lesson also learnt the hard way.
With my sons almost magically coordinated with our backless gowns we seem to be ready. Using the left over fabric from shortening our dresses Marie created bow ties and a cumberbun for Josiah to match. I will have to admit however I did have to really talk my both my sons into agreeing to wear the pink bow ties that had been designed for them. Now with their suits pressed we are all looking so forward to this wonderful evening.
While I anxiously await this special evening with my sons I cannot help but think about changes. Not only changes age has made on me but changes the life I am called to live requires of me. My life with Duchenne at times demands of me to surrender and adapt to changes. Changes that I am not always eager to embrace or accept. The effect that this disease has had on my life is so great that even my fashion style has been effected. I will always admire the glittery, and delicate clothing I once could adorn freely. It will always be in me to secretly want to bare my shoulders or cover myself in sequence. The shoes I buy now will have a somewhat lower modest heel to help me stay balanced when lifting more than my weight. On occasion I hope to still attend events that will allow me the opportunity to borrow a few accessories from my younger sisters more youthful wardrobe. I will however let her keep the stilettos on her feet and accept that I must be a bit more grounded and at times even more modest to meet the tender needs of my sons.
Sunday, March 25, 2012
my image
Josiah sat next to me brushing his teeth. While I brushed my hair looking in his large bathroom mirror, I glanced over at him. I was so happy and proud that he could still manage this task by himself. Reaching over towards him I placed a free standing counter mirror in front of him, just in case he wanted to see for himself the beautiful job he was doing. Josiah kept busy with his grooming and never glanced over at the mirror. Smiling at him I suggested he see how gleaming white his teeth looked. He just smiled and continued with his brushing. However something clicked in me at that precise moment. It was almost as though I heard a soft whisper in my ear. A voice, telling me something was very wrong here. Something, that he had been hiding inside would now make my heart ache for him.
I knelt down next to Josiah to actually see what he was capable of seeing in the mirror at his level. The large wooden framed mirror above his bathroom vanity just grazed the top of his head with his reflection. It was not to surprising to me that sitting in his desk chair the height was not exactly perfect for him, to admire his beauty. We had designed his sink counter top to fit the height of his wheelchair. Now with the counter mirror in front of him clearly he was well with in his range of viewing. Tilting it some more toward him, I encouraged Josiah to take a peek. Having just finished brushing his teeth, he wiped his face with his head still turned away. Somewhat giggling but very anxious to just be done he tried to scoot out of the room. "Josiah" I cooed "you have to see how beautiful your smile is". The closer I moved the mirror the more he angled his head to avoid his reflection. Gently I reached out to raise his chin. Slowly his smile faded. As he softly spoke my eyes watered. His beautiful little face looked up into mine with tears and almost whispering he told me he looked ugly.
Its moments like this that break my heart. I did not think a day had ever passed by where I had not praised my boys for their beauty and abilities. I had seen Josiah look at photos of himself. Never ever did I notice him to shy away from being photographed. Kneeling at his side I looked into the very sad eyes of my youngest, absorbing the pain he was sharing with me. How could this have happened? Holding him tightly in my arms, questions raced through my mind. What caused my beautiful boy to feel so bad that he could not look at himself in the mirror? Why did I not notice this sooner? Where was I when this happened? Most importantly what evil had made my child feel so badly?
We have all heard stories about bullying. Stories that have often brought us to tears because of the tragic, damaging harm it can cause. Hurting because as caring human beings it pained us to see others suffer. I know many of us have even been victims ourselves and can deeply understand this pain. I wanted to some how free my child from this hurt. Erase this horrible belief that he had accepted into reality.
Slowly and and with teary eyes Josiah confided in me the secret pain he had been hiding. He was well aware of the stares in public he receives. That was one hardship he dealt with, but recently he had also been the target of insults from some females at school. Ugly, was the word that seemed to have hurt him the most. The recent progression of his muscle disease has caused changes in his physical appearance, only enforcing his belief in the disastrous meaning of the ugly word. Very aware of the effects his limited ability causes, he longed to be like any other teenager, however in reality as harsh as it sounds, invitations are almost nonexistence and friends are not exactly lining up at the door to hang out with him.
I held him in my arms while he talked, fighting back my own rage that someone had caused my child so much pain. Together we both made it through that long tearful day. I manged to get Josiah to glance at himself in the mirror later that afternoon. It appeared his contagious smile had returned. Deep inside I felt so much sorrow that my son had to experience this sort of pain in addition to his daily suffering. He would have to continually accept the changes Duchenne will cause and would undoubtedly experience yet more low moments. I desperately wanted to cling to hope that he will see all the beauty he truly posses one day soon and love what he sees. As sad as it is though no matter how hard I tried to help him he would have to continue to share the world with ignorant unkind humans, something I could no more control than the weather. But, I will not give up on trying to change the effects these unkind words have on him. I am determined to keep all those that see him as the remarkable young man that he is close, very close at times.
Talking to Josiah's school and addressing the issue has opened many eyes and is provoking more awareness. While the episodes appear to have been isolated they are still being addressed. As a realist I do not believe for a second it will not happen again. I still will have concerns that Josiah somehow feels he has to hide things, even from me. Not only do bullied children often feel isolated but fear contributes to them hiding their pain. A child with a terminal disease often will try to hide anything outside thier disease for fear of feeling even more isolated. Just being aware as parents that more may be going on, is all we can do at times.
I know I can not protect Josiah from everyone and he will over hear things that may make him feel sad from time to time. The harsh reality of the world is, we as humans can be cruel even with out intending to be aka; sarcasm.
It pleases me though that I can see true joy and happiness with in my sons. I am so proud that all three of my sons do feel very loved and that I have managed to make that very apparent. Outside in the world beyond, the reality is- as parents, there will be moments when we will have to be a warrior for our children. That can be very tough and disheartening at times. Quite frankly in all honesty it causes me to deal with my own disgust towards society and acceptance. When I reentered into the dating world seven years ago, while my appearance may have placed me on a list to be desired the fact that I had 2 sons with special needs set me very much aside. Thankfully my happiness has never relied on the fate of falling in love. But as humans we all want to belong and have a place in this world that gives us that sense of self worth, most importantly though we need to be loved. I know my son is not alone and my heart goes out to all of us who have felt less at times.
As I have grown stronger on my journey I know " I would rather shine alone than be lost in the crowd" and as long as I am here" I will help my sons to always shine".
I knelt down next to Josiah to actually see what he was capable of seeing in the mirror at his level. The large wooden framed mirror above his bathroom vanity just grazed the top of his head with his reflection. It was not to surprising to me that sitting in his desk chair the height was not exactly perfect for him, to admire his beauty. We had designed his sink counter top to fit the height of his wheelchair. Now with the counter mirror in front of him clearly he was well with in his range of viewing. Tilting it some more toward him, I encouraged Josiah to take a peek. Having just finished brushing his teeth, he wiped his face with his head still turned away. Somewhat giggling but very anxious to just be done he tried to scoot out of the room. "Josiah" I cooed "you have to see how beautiful your smile is". The closer I moved the mirror the more he angled his head to avoid his reflection. Gently I reached out to raise his chin. Slowly his smile faded. As he softly spoke my eyes watered. His beautiful little face looked up into mine with tears and almost whispering he told me he looked ugly.
Its moments like this that break my heart. I did not think a day had ever passed by where I had not praised my boys for their beauty and abilities. I had seen Josiah look at photos of himself. Never ever did I notice him to shy away from being photographed. Kneeling at his side I looked into the very sad eyes of my youngest, absorbing the pain he was sharing with me. How could this have happened? Holding him tightly in my arms, questions raced through my mind. What caused my beautiful boy to feel so bad that he could not look at himself in the mirror? Why did I not notice this sooner? Where was I when this happened? Most importantly what evil had made my child feel so badly?
We have all heard stories about bullying. Stories that have often brought us to tears because of the tragic, damaging harm it can cause. Hurting because as caring human beings it pained us to see others suffer. I know many of us have even been victims ourselves and can deeply understand this pain. I wanted to some how free my child from this hurt. Erase this horrible belief that he had accepted into reality.
Slowly and and with teary eyes Josiah confided in me the secret pain he had been hiding. He was well aware of the stares in public he receives. That was one hardship he dealt with, but recently he had also been the target of insults from some females at school. Ugly, was the word that seemed to have hurt him the most. The recent progression of his muscle disease has caused changes in his physical appearance, only enforcing his belief in the disastrous meaning of the ugly word. Very aware of the effects his limited ability causes, he longed to be like any other teenager, however in reality as harsh as it sounds, invitations are almost nonexistence and friends are not exactly lining up at the door to hang out with him.
I held him in my arms while he talked, fighting back my own rage that someone had caused my child so much pain. Together we both made it through that long tearful day. I manged to get Josiah to glance at himself in the mirror later that afternoon. It appeared his contagious smile had returned. Deep inside I felt so much sorrow that my son had to experience this sort of pain in addition to his daily suffering. He would have to continually accept the changes Duchenne will cause and would undoubtedly experience yet more low moments. I desperately wanted to cling to hope that he will see all the beauty he truly posses one day soon and love what he sees. As sad as it is though no matter how hard I tried to help him he would have to continue to share the world with ignorant unkind humans, something I could no more control than the weather. But, I will not give up on trying to change the effects these unkind words have on him. I am determined to keep all those that see him as the remarkable young man that he is close, very close at times.
Talking to Josiah's school and addressing the issue has opened many eyes and is provoking more awareness. While the episodes appear to have been isolated they are still being addressed. As a realist I do not believe for a second it will not happen again. I still will have concerns that Josiah somehow feels he has to hide things, even from me. Not only do bullied children often feel isolated but fear contributes to them hiding their pain. A child with a terminal disease often will try to hide anything outside thier disease for fear of feeling even more isolated. Just being aware as parents that more may be going on, is all we can do at times.
I know I can not protect Josiah from everyone and he will over hear things that may make him feel sad from time to time. The harsh reality of the world is, we as humans can be cruel even with out intending to be aka; sarcasm.
It pleases me though that I can see true joy and happiness with in my sons. I am so proud that all three of my sons do feel very loved and that I have managed to make that very apparent. Outside in the world beyond, the reality is- as parents, there will be moments when we will have to be a warrior for our children. That can be very tough and disheartening at times. Quite frankly in all honesty it causes me to deal with my own disgust towards society and acceptance. When I reentered into the dating world seven years ago, while my appearance may have placed me on a list to be desired the fact that I had 2 sons with special needs set me very much aside. Thankfully my happiness has never relied on the fate of falling in love. But as humans we all want to belong and have a place in this world that gives us that sense of self worth, most importantly though we need to be loved. I know my son is not alone and my heart goes out to all of us who have felt less at times.
As I have grown stronger on my journey I know " I would rather shine alone than be lost in the crowd" and as long as I am here" I will help my sons to always shine".
Sunday, February 5, 2012
Do I believe
At first I felt nothing. Listening to him I felt numb, as though all life had just been drained from me. I stood frozen unable to move or think. I watched as the Doctors lips moved while he spoke to me. His tired red eyes teared as he looked into mine. Deep inside me, I already somehow knew what he was telling me. But now listening to him it became my heartbreaking reality.
For some reason memories of sitting in my prenatal classes amongst all the other happy anxious parents to be- flashed through my mind. Maybe, it was because for the first time in my life I finally felt like I had a purpose, a real meaning to be here, in this world. A time in my life when I was in love and over joyed to be living my dream. I was with child and cherishing how alive it made me feel. I drifted back to a place in my life when I was surrounded by other females, who also embraced this new adventure. Other young women, excited, scared, and in love with the life that grew inside of them. Together we sat in the arms of our partners, expressing our fears, anticipation and the expected joy that was ahead. Briefly I returned to a time when I did not feel betrayed by faith and was not tormented by death.
The present interrupted me abruptly. Very softly spoken I heard the words "I am sorry". A single tear trickled down my cheek. In an instant my world changed. At that precise moment all that I had hoped and dared to dream left me. I stood motionless with my heart shattered, knowing all to well this pain I was feeling right now, was only the beginning of my new journey.
Holding my beloved child in my arms, slowly, I unleashed my sorrow. As tears silently streamed down my face I felt pieces of me die. Desperately, I wanted to feel the same joy I felt when he was born. His beauty captivated me as I looked down at this perfect little baby that I held. " I am sorry" echoed in my head. All around me I felt our world crashing and there was nothing I could do to stop it. I was sorry too. Sorry, that after all these years the medical world still had no treatment or cure for Duchenne. Sorry that more boys would still have to endure all the pain living with Duchenne caused. Sorry, that we would have to continue to cling to hope for a cure to get through each day. Most importantly, sorry that my beautiful baby would be sentenced to a life of living with a devastating disease, that shows no mercy in its unrelenting attack on the human body. Sorry that my son would slowly suffer from a disease that would eventually take his life far to soon, only after imprisoning him for years.
Often I will see or read something that triggers a memory from an event of my past. Awakening emotions neatly buried inside, quietly resurfacing. In those moments I am left with explosions of feelings and stirring memories. Experiences that scream to be unleashed with a purpose to be shared in some enlightning way. I read a posting today on FaceBook regarding the question, "Who believes in miracles?" Something deep inside me stirred. While reading some of the responses I came across one response that said, " No I do not believe in miracles, every thing is cause and effect". I stared at the word "no" for awhile. Only one response from a DMD mother had answered differently to that question.
It was over 20 some years ago when Duchenne personally reappeared into my world.
Those feelings when my son was first diagnosed controlled me for months. At times almost making getting out of bed impossible. Somehow though I did. I found the courage and strength to accept every challenge that laid ahead of us. But if you had asked me in those first few months if I BELIEVED IN MIRACLES- my answer would have been NO. It would have been an answer coming from heartache and fear. It would have came from a mother who felt despair consume her after being just told her son had an expiration date. That her beautiful child was diagnosed with a terminal disease and there was no treatment or cure.
Today I am a single mother of three sons. most of you know my two youngest sons both suffer from an unrelenting fatal disease. They also struggle with a cognitive delay. The past 12 years of raising them alone has been anything but miraculous. We have struggled through some very difficult times that personally has only made me stronger in my perseverance to see my sons and I succeed. Do I believe in miracles the answer is, yes. Do I think I have personally experienced a miracle the answer is no, but I will admittedly share I have felt the touch of a higher power at times.
What I have experienced is that even with the devastating effect Duchenne has had on my sons and I there have been moments when I have also felt the presence of something more powerful with us. I have seen my sons loose the ability to walk, to raise their arms above their heads. I have watched them completely become dependent on me for things most of us take for granted, like scratching the top of their nose, or rolling over in bed. But I have also watched them triumph through loss.
So yes, I believe miracles happen. But I am not willing to sell it short. It is not miraculous that I have raised three sons by my self. That I have been responsible in providing for all the care in meeting my two younger sons special needs, while helping to put my eldest son through college as a single parent. That is the effect of hard work and personal sacrifice. While I am thankful my sons are still with me and we live comfortably, it is the effect of my unconditional love and commitment to care fort them and part of Gods plan to have my sons still with me. But if Cody or Josiah rose out of their wheelchair tomorrow and stood unsupported, yes, that would absolutely be miraculous. If love walked through the door and swept me off my feet today that might just qualify as miraculous too.
The joy we feel when we first hold our new born child can almost be described as a miraculous feeling. Some times some of us will refer to finding the one with whom we want to spend the rest of our life with as miraculous. In any event the belief in miracles is not meant to challenge us. Believing in miracles helps us to survive the negative effects of this world and that in itself is a blessing.
I do believe where there is love great things can happen. I believe Angels exist and walk amongst us. I feel prayer is powerful to the heart and mind and that hope and faith is essential to surviving tragedy. I also believe that there is a great plan and we are all a very important part of Gods design.
The thought of something miraculous gives us hope and in times of despair for some of us that might be all we have to hold onto in this world.
For some reason memories of sitting in my prenatal classes amongst all the other happy anxious parents to be- flashed through my mind. Maybe, it was because for the first time in my life I finally felt like I had a purpose, a real meaning to be here, in this world. A time in my life when I was in love and over joyed to be living my dream. I was with child and cherishing how alive it made me feel. I drifted back to a place in my life when I was surrounded by other females, who also embraced this new adventure. Other young women, excited, scared, and in love with the life that grew inside of them. Together we sat in the arms of our partners, expressing our fears, anticipation and the expected joy that was ahead. Briefly I returned to a time when I did not feel betrayed by faith and was not tormented by death.
The present interrupted me abruptly. Very softly spoken I heard the words "I am sorry". A single tear trickled down my cheek. In an instant my world changed. At that precise moment all that I had hoped and dared to dream left me. I stood motionless with my heart shattered, knowing all to well this pain I was feeling right now, was only the beginning of my new journey.
Holding my beloved child in my arms, slowly, I unleashed my sorrow. As tears silently streamed down my face I felt pieces of me die. Desperately, I wanted to feel the same joy I felt when he was born. His beauty captivated me as I looked down at this perfect little baby that I held. " I am sorry" echoed in my head. All around me I felt our world crashing and there was nothing I could do to stop it. I was sorry too. Sorry, that after all these years the medical world still had no treatment or cure for Duchenne. Sorry that more boys would still have to endure all the pain living with Duchenne caused. Sorry, that we would have to continue to cling to hope for a cure to get through each day. Most importantly, sorry that my beautiful baby would be sentenced to a life of living with a devastating disease, that shows no mercy in its unrelenting attack on the human body. Sorry that my son would slowly suffer from a disease that would eventually take his life far to soon, only after imprisoning him for years.
Often I will see or read something that triggers a memory from an event of my past. Awakening emotions neatly buried inside, quietly resurfacing. In those moments I am left with explosions of feelings and stirring memories. Experiences that scream to be unleashed with a purpose to be shared in some enlightning way. I read a posting today on FaceBook regarding the question, "Who believes in miracles?" Something deep inside me stirred. While reading some of the responses I came across one response that said, " No I do not believe in miracles, every thing is cause and effect". I stared at the word "no" for awhile. Only one response from a DMD mother had answered differently to that question.
It was over 20 some years ago when Duchenne personally reappeared into my world.
Those feelings when my son was first diagnosed controlled me for months. At times almost making getting out of bed impossible. Somehow though I did. I found the courage and strength to accept every challenge that laid ahead of us. But if you had asked me in those first few months if I BELIEVED IN MIRACLES- my answer would have been NO. It would have been an answer coming from heartache and fear. It would have came from a mother who felt despair consume her after being just told her son had an expiration date. That her beautiful child was diagnosed with a terminal disease and there was no treatment or cure.
Today I am a single mother of three sons. most of you know my two youngest sons both suffer from an unrelenting fatal disease. They also struggle with a cognitive delay. The past 12 years of raising them alone has been anything but miraculous. We have struggled through some very difficult times that personally has only made me stronger in my perseverance to see my sons and I succeed. Do I believe in miracles the answer is, yes. Do I think I have personally experienced a miracle the answer is no, but I will admittedly share I have felt the touch of a higher power at times.
What I have experienced is that even with the devastating effect Duchenne has had on my sons and I there have been moments when I have also felt the presence of something more powerful with us. I have seen my sons loose the ability to walk, to raise their arms above their heads. I have watched them completely become dependent on me for things most of us take for granted, like scratching the top of their nose, or rolling over in bed. But I have also watched them triumph through loss.
So yes, I believe miracles happen. But I am not willing to sell it short. It is not miraculous that I have raised three sons by my self. That I have been responsible in providing for all the care in meeting my two younger sons special needs, while helping to put my eldest son through college as a single parent. That is the effect of hard work and personal sacrifice. While I am thankful my sons are still with me and we live comfortably, it is the effect of my unconditional love and commitment to care fort them and part of Gods plan to have my sons still with me. But if Cody or Josiah rose out of their wheelchair tomorrow and stood unsupported, yes, that would absolutely be miraculous. If love walked through the door and swept me off my feet today that might just qualify as miraculous too.
The joy we feel when we first hold our new born child can almost be described as a miraculous feeling. Some times some of us will refer to finding the one with whom we want to spend the rest of our life with as miraculous. In any event the belief in miracles is not meant to challenge us. Believing in miracles helps us to survive the negative effects of this world and that in itself is a blessing.
I do believe where there is love great things can happen. I believe Angels exist and walk amongst us. I feel prayer is powerful to the heart and mind and that hope and faith is essential to surviving tragedy. I also believe that there is a great plan and we are all a very important part of Gods design.
The thought of something miraculous gives us hope and in times of despair for some of us that might be all we have to hold onto in this world.
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