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Muscular Dystrophy Association

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Nonprofit Overview

Causes: Health, Nerve, Muscle & Bone Diseases, Nerve, Muscle & Bone Diseases Research

Mission: The Muscular Dystrophy Association is a voluntary health agency, a dedicated partnership between scientists and concerned citizens aimed at conquering more than 40 neuromuscular diseases that affect more than a million American adults and children. The diseases in MDA''s program include nine forms of muscular dystrophy, amyotrophic lateral sclerosis (Lou Gehrig''s disease), spinal muscular atrophy, Charcot-Marie-Tooth disease, metabolic diseases of muscle, myasthenia gravis, inflammatory myopathies, CMT, SMA, and other neuromuscular conditions.

MDA combats these diseases through programs of worldwide research, comprehensive medical and community services, and far-reaching professional and public health education. The Association''s programs are funded almost entirely by individual private contributors.

Programs: Local businesses sell green shamrock mobiles for $1 donation to MDA and gold shamrock mobiles for a $5 donation to MDA.  The program runs February - March every year.

Community Stories

2 Stories from Volunteers, Donors & Supporters



Rating: 5

I am not quite sure why only the Sharmock program is listed, but notice none of the previous reviews are specific to it. I wasn't sure if I should list myself as a volunteer or client served, as I am both of these! After several years of searching for answers to my medical issues, I was finally directed to the MDA Clinic at Northwestern University in Chicago. My daughter and I were both diagnosed with Charcot-Marie-Tooth disease on our intial visit. I made a decision at that time (2003) to also have DNA testing done to save any other members of my family the painful extensive process I went through. At that point in time the MDA covered the cost of the testing. My daughter and I continue to this day attending this clinic every 6 to 12 months. In 2007, my daughter gave birth to my first grandchild, Hunter. It became apparent by the time he was 2 1/2 that Hunter was exhibiting symptoms of CMT. An appointment was made at the pediatric clinic at Rush University and getting a specific diagnosis of a child of this age with a painful ncv/emg was not an option. At this point in time the MDA was no longer absorbing the fee for the DNA testing and his insurance didn't cover it either. We felt at an impass. Then something rather amazing happened. The pediatric neurologist contacted our MDA health care co-ordinator and received approval for the payment within 20 minutes. Each clinic has some discretion with their MDA grant money and our family is forever greatful!

I have to be honest and say that, prior to Hunter's diagnosis, the thought of volunteering had never even entered my mind. My knowledge consisted only of the telethons that interupted the Cubs games on Labor Day weekend! I also felt powerless over his illness, it affected me much more than my own and my daughter's, who was older (16) when she was diagnosed and had very little symptems at that point in time. The first program we became involved with was Shamrocks for Dystrophy. I voiced my concern about not wanting Hunter paraded around for sympathy to raise money, turns out Hunter is quite a natural entertainer and really enjoys doing it. I beleive the next project was the Summer Camp Medallions. We worked with Hunter's school to participate in the Hop-a-Thon and with our local fire department to bring the Fill-the Boot program to the town we live in. The last 3 years we have fielded Team Hunter's Heroes in the MDA Chicago Muscle Walk. All 3 of us have been part of clinical research currently being funded by the MDA as well. Two years ago Hunter was finally old enough to go to MDA Camp. It was kind of a difficult decision to let him attend at such a young age and when he got there he refused to get out of the car! When camp was over, he didn't want to leave! He has made a wonderful friend in his camp "buddy" Nicole, who continues to maintain a relationship with Hunter. She has taken him to the zoo and bowling and just to hang out. I take exception to a previous comment regarding the summer camp program simply being a photo opportunity. Hunter had his 2nd trip to camp recently and it's very clear to me that this program has and will continue to make a lasting positive effect upon him. He also understands the concept that the events he participates in help pay for him and other kids like him to have a camp experience. Many of these children would never be able to attend any other camp due to their special needs, to me that's pretty relevant!

I/we (https://www.facebook.com/HuntersQuesttocureCMT) as Hunter's Heroes, choose to fundraise because sitting by and doing nothing to help find a treatment/cure for Hunter is not an option. We have worked with CMT specific charities in the past and made a decision to work solely with the MDA because of the benefits we reviece directly and indirectly from them. They currently fund more CMT specific research (and the list of projects is readily accessable) than any charity, provide team approach clinics at no fee, have excellent local support teams (who know us by name) and much more.


Rating: 5

I have participated with MDA's Locked Up program consistently over the past 5 years or so. The fundraising coaches are very helpful and have great ideas on how to help me reach goals and really make a difference. This was the first charity I have worked with and I was very new to fundraising but I feel like an old pro now. I really like how their support goes to local families in my area as well as to national research. We had the opportunity to meet some of the children with MD at the last Lock Up event it was really rewarding to be able to help. Please participate if you havent before. Great cause!!!