The funny thing is I am originally from Minnesota. I now live in Arizona and have met no one with my condition here. I too am 24 years old. I noticed signs of weakness senior year of High School. I wasn't running as fast as I used to and figured that I was just out of shape. Around that time I went through testing to join the army. They found that my calf muscles were not the average size which made it impossible for me to complete some of their physical tests. I went through many tests just as you did and then found that I had Miyoshi Myopathy. My doctor prescribed creatine and CoQ10 for me. However, I tend to forget to take those so I don't really know if they work well. I am going to get married in a year. She came into the relationship completely aware of the situation. I warned her that I may be in a wheelchair someday. I think
that day will be soon. I am having difficulty walking normal even with braces. I am thinking about an electric chair and hand controls for my car when my situation requires them. It's really nice to meet someone in the same age group with this type of disease. I don't feel so alone anymore. I hope we can keep in touch and discuss more about common experiences or new knowledge.
samanthasmith7 <hushfire777@...> wrote:
Hi, my name is Samantha and I was diagnosed in March of 2007 with LGMD2B at the age of
24. I first started showing signs of weakness at the age of 20 but contributed it to a car accident I was in where I was ejected out of the vehicle. I got pregnant in March of 2006 and had a complicated pregnancy. I was about 5 months along when I started noticing that I was getting weaker. I had problems getting up the stairs without using the handrail. My daughter was born in December and within 3 months it became nearly impossible to get up the stairs or getting up on my tip toes. I was referred to Mayo Clinic in Rodchester, Minnesota where I have had every test imaginable to confirm my diagnosis. Now, almost a year after being diagnosed I am finally coming to terms with it. I've been extremely angry and incredibly sad about being diagnosed with such a disease. I worry about being able to do things with my daugher, now 14 months, and her and my fiance having to take care of me in the future. My family and I have
jokingly called me an "ostrich" because I have not wanted to face this. So until recently I have had no interest in trying to get better, no matter what the method may be. As a result, I am already a stage weaker. Now I am really scared. As many of you have found, not much information is available on this disease, what makes the process slower, or what "cures" it. It is also near impossible to find someone who has it. That is why I am so happy to be a part of this group. I can't wait to speak to someone, anyone, who is going through what I am and to hear what kind of things you are doing to treat this disease.
Hi, my name is Samantha and I was diagnosed in March of 2007 with LGMD2B at the age of 24. I first started showing signs of weakness at the age of 20 but...
Hello, my name is John The funny thing is I am originally from Minnesota. I now live in Arizona and have met no one with my condition here. I too am 24 years...
Hi, my name is Miriam.. I am from San Francisco, about to turn 21 years old. I started to notice signs of weakness during my senior year in highschool as well....
Hi! I'm Ron and I'm from Southern California and have never met anyone else with Miyoshi Myopathy or LGMD2B. I first noticed that I couldn't stand on my toes...
Hi Ron!! I am sorry that I did not respond to your message right away. I first read your message almost a week ago now. First, I must say that it is nice to...
Hey Samantha! The article link on vitamins was very interesting. I have tried multi vitamins too but for some reason I seem to get an allergic reaction from...
Hey Ron! I'm glad that you got a chance to read that article. I have not personally had any alergic reactions to vitamins. My father is a chiropractor and has...
Hey Sam! Actually I am an M.D., so it shouldn't be a problem for me to get the vitamins. Let me know the details. I've been recently trying B12 shots too and...
Ron- No wonder you are so well informed and are active in treatments. How long have you been doing the B12? Energy is something I am lacking so I am interested...
Hey Sam! Just started taking the B12 shots a few months ago. I usually do a weekly injection. So far it seems to reduce the speed of fatigue, increases my...
Hi Ron, Thank you for sharing your information. I had considered using 'protein shakes' (partly because I'm a vegetarian and was concerned that I might not be ...
Hey Rebecca! I've heard that having having alot of excess protein can be hard on the kidneys but I don't think anybody really knows how much protein is needed...
Hi Ron, Thanks for your response, I totally agree with the sentiment and am grateful for the information! Recon I'll give the protein shakes a go (in...
Ron- Thanks for the info. I am contacting my doctor today about the b12 shots. What is your weakly dose? I haven't sent you anything on my physical therapy...
Hi Samantha, I would go relatively easy on the physical therapy and physical exertion generally. In my experience it is very helpful to do what you can each...
Hey Josh! I think that there is alot of variablility to how much exertion one is able to do with this disease. Like I said in a recent previous post, no one...
Hi Miriam! Thank you so much for responding. I have had the same tests and muscle biopsy. My doctors in the beginning gave two ideas for diagnosis and that...
Hi I'm Suzanne, from Surrey England. I'm 39 now but started my symptoms back in my early twenties. I just wanted you to know that it's not the end of the...
Thank you for posting Suzanne, really good to hear something positive. I've just turned 30 and may want to have children myself one day... so I would be really...
Hi Rebecca. I have a little knowledge about this disease and how it effected me during my pregancy. I had a slightly complicated pregancy. I started to go...
Hi Samantha, Thank you very much for your reply. Sorry it has taken me a while to get back to you. I'm so happy to hear that your daughter is well, and that...
THANK YOU!!! THANK YOU SO MUCH!!! I am crying now just reading what you have wrote. I thought that there was light at the end of the tunnel, now I know there...
Samantha - I'm glad that you're a part of this group. It's always comforting to learn that others experience the same things. On a personal note, my wife and I...
Thank you!! I am familiar with the jain foundation. How fortunate are we to have such an amazing advocate on our side? With the support of my family we are...
Hi everyone, I haven't written in a long time but the recent activity it's made me want to write in. I'm 28 years old and was diagnosed with Miyoshi Myopathy...
Bryan- Here is what I know about dysferlinopathy, dysferlin, and muscle enzyme levels. Dysferlin and muscle enzymes are two different things. Dysferlin is a...
Dear Bryan, My name is Laura Rufibach and I work for the Jain Foundation. The Jain Foundation (www.jain-foundation.org) is a non-profit organization dedicated...
Hi, My name is Roxie and I am 30yrs old. I have 2 beautiful children ages 5 and 2 and a wonderful husband. I was diagnosed with LGMD2B in Sept. 2007. I was in...