Tags:
hi my name is vilma and i have a 21 year old ismael with dmd. feeling guillty is normal but you can turn this around into a positive experience for you.first your faith tells you that Dylan is in a wonderfull place where he is not suffering and that you will see him again someday. you where not the reason he is gone duchennes is and that's why we are joining this parent project to end it, but until this happens we are going to loose some of our precious children and we need to focus on what's important family and quality of life for this children and their siblings.you are Dylan's mom but also David's and you have a loving husband that also needs you .I learn from my son to focus on what i can do and dont dwell on what i cant . Dylan want to see his family be happy and content allow it to happen some times guilt can keep us from being happy but remember Dylan wants you to be happy he will always be alive and a part of all of you, is going to take some time but with love, patience and lots of prayers it can be done. if you need to talk you can contact me i understand your feelings i've being there.
my love and prayers are with you and your family
Vilma, you are an inspiration. I had 2 sons as well, and they are now RUNNING down the streets of Gold! I am a carrier of Duchenne, and there is no family history of it. My sons were diagnosed in 1990 and 1991 at the ages of 5 and 2. I had taken the 5 year old to dr after dr, to be told all sorts of reasons why he wasn't doing the things motor skill wise that he should have been doing at his age. I heard everything from "diaper waddle" to "flat footed". It was very discouraging. Actually finding out the final diagnosis was a blessing, because at that point we learned what we were dealing with, and that is always better than the unknown. I went through every stage there was out there, from denial to anger to self pity to ok...bring it on. Without my faith, I would have been lost. My sons were very bright, and asked questions all the time. All I knew was to be honest with them, and tell them as much as their little brains would absorb. The one thing I learned with them was that it didn't matter what they couldn't do. They were more interested in what they could accomplish. Yes, they wanted to be able to keep up with the other kids, but really, who was it that wanted it more...them or me? When my oldest son passed away, he left a huge legacy behind. We lived in a small town, but there were more than 700 people at his funeral. He was in the show choir at his high school, was the choir king, was in the all state choir, and sang in a barbershop chorus. He received most improved choir member two years in a row, and had a scholarship to OSU in vocal music. This all with a lung capacity that was 46%. He was amazing, but his faith was even more amazing. The one thing I have to be thankful for is that when he did pass away, it was very quickly, a blood clot to the lung which killed him instantly. He was not sick prior to this, and he did not suffer. That was August 2006. I still grieve for him...but I know where he is, and I know I will see him again.
My youngest son, Jeremy, was his own person as well. He had a totally different personality than his brother, but just as amazing. He even got married just after he graduated high school. This was particularly difficult for me, because I knew that he would lose his health insurance benefits and would only have state medicaid to rely on, but I had told him his entire life that he was just like everyone else, had the same desires and needs, and then at the age of 18 I was trying to change the rules. He RAN into the arms of Jesus on March 1, 2009. Once again, he left his legacy, his heart, his friends, but he did it one his terms, very quickly. We aren't sure if he had a cardiac arrest, or if he had a pulmonary embolism, but he went quickly, without being sickly.
I grieve for them on a daily basis. But, their wit, their personality shines on a daily basis. They taught me so much. They taught me that you have to choose your battles, everything can't be a battle, and make sure you have your guns loaded when you are ready to fight. Your fights come with schools, insurance companies, people who lack understanding, and people who are just down right mean. The one thing I know is that they still live in my heart, as well as everyone they came in contact with. I have a daughter who is 28, and thankfully she is not a carrier. She has blessed me with 3 beautiful grands, and I am able to absorb my time with them and my job, while trying to help teach others how to be an advocate for their kids. Working in the field I do, every day I get the opportunity to share the knowledge I have acquired over the past 21 years for the benefit of others. God bless each of you...
vilma rodriguez said:
hi my name is vilma and i have a 21 year old ismael with dmd. feeling guillty is normal but you can turn this around into a positive experience for you.first your faith tells you that Dylan is in a wonderfull place where he is not suffering and that you will see him again someday. you where not the reason he is gone duchennes is and that's why we are joining this parent project to end it, but until this happens we are going to loose some of our precious children and we need to focus on what's important family and quality of life for this children and their siblings.you are Dylan's mom but also David's and you have a loving husband that also needs you .I learn from my son to focus on what i can do and dont dwell on what i cant . Dylan want to see his family be happy and content allow it to happen some times guilt can keep us from being happy but remember Dylan wants you to be happy he will always be alive and a part of all of you, is going to take some time but with love, patience and lots of prayers it can be done. if you need to talk you can contact me i understand your feelings i've being there.
my love and prayers are with you and your family
© 2023 Created by PPMD.
Powered by
Badges | Report an Issue | Privacy Policy | Terms of Service