Kids with MS
I read this article recently about kids with multiple sclerosis. I didn't realize children could develop the disease. The University of California San Francisco has a well-known multiple sclerosis center which has been studying children with the disease. It's thought that there are probably many cases of this, but most go undetected as they are dismissed by the parents or doctors who don't consider MS to be a childhood disease.
I would imagine their youth would be an asset, as young people tend to recover more quickly and are generally more healthy than adults. Of course, that would be balanced with the fact that they developed the disease very early in life, so they have many more years to deal with the disease.
In the article, a 12 year old girl mentions how she's getting used to the medication even though it hurts. For all those out there afraid to start treatment because of needles: Look at this brave little girl who's taking her shots and, in doing so, some control over her life. She's an inspiration.
Here's some more information about pediatric MS from the National Multiple Sclerosis Society.
Comments
I was diagnosed in 2000 when I was just 13. I had Optic Neuritis when I was just 8. Ever since the ON I suffered different symptoms with MS and no one knew what was wrong with me. I was so sick of doctor after doctor listen to my symptoms and say, "I've never seen this before." It was frustrating to say the least. It was such a relief to finally have a dianosis and understand that someone knew what my symptoms were. I'm now a 20 year old junior in college, right now I'm working full time. I have relapsing-remitting MS and I struggle with it everyday, but it's just another trial. I've been on Avonex since I was dianosed and I am so grateful for the good health I've had these years and all that I've been able to acomplish. I also have an identical twin sister who suffers from the same type of MS, so at least I have someone close to me all the time who really understands my symptoms as well.
Posted by: Brooke | July 4, 2007 08:41 PM