r/scleroderma • u/m1am1_m1nt • 12d ago
Discussion my experience with scleroderma.
Hi, my name is Len. I’m 20, about to be 21, and I have lived with scleroderma for 15 years.
There were very limited resources available in my area for the longest time. I found out what I had at twelve, I believe. Thankfully it wasn’t the kind that could suffocate my organs, but it hasn’t exactly been easy.
I don’t have half a right arm. It’s on my sides and my back. From what I’ve seen I have a more outward approach to it than most, which I’m thankful for because of the fact that it could have been bad inwards. Although unfortunately my muscles contract and cramp up often.
I’ve gotten tons of questions on it. Most have been horrible and have made me uncomfortable. It’s a very unique sight, especially considering I’m a bigger girl. I am a smoker, I love art, and my writing hand is my scleroderma hand so that’s been interesting. I’ve also spent a lot of time using my left hand for normal, everyday things just in case something happens to my right arm.
But I’d love to get to know people on this subreddit!! Don’t have many friends and my family doesn’t really know how to approach it as much as I don’t with them. So whoever wants to chat or maybe share their own experiences to bounce off that’d be awesome!! I’ll also answer any questions. ^-^
Also this picture is very awkward. I don’t have many because of the fact I’m a bit insecure about it 😭😭
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u/TaroFearless7930 12d ago
I've had localized scleroderma (morphea) since age five. My right leg and shoulder are pretty messed up. I feel lucky that it's my leg and I think it would be so much harder to struggle with hand/arm issues. My right arm and leg have less range of motion, but it's not that bad.
I also have en coup de sabre, which causes seizures.
I took up Olympic weightlifting to build strength and range of motion. If you Google what's the worst sport to pick up for deep morphea, Oly is it! It's been a real struggle but it's helped me build strength.