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Oh my god....what's next! Anyway Lily...do you have an email address? I said in my post, which was about 3 paragraphs long and took a long time to type due to the atrophy in my hands, that I would private message you when you were able to accept them. I am not sure why that, along with...

That's exactly what I have said to my neurologists. What are the chances that I was doing fine, then became ill with 4 different diseases.....No way! I keep thinking if they would get to the bottom of it, they could stop my progression. Thanks John.

Yes, and I can't believe there is someone with the exact same diagnoses as me. I have only been on Prednisone for 5 months and as soon as I tapered down the symptoms did get worse. Yet, the side effects of the Prednisone are somewhat bad too. I am also taking aspirin everyday and the rheumo...

I also have a high prothrombin time (antiphospholipid antibody syndrome), myopathy and have tested positive and negative for lupus anticoagulant (it changes it's mind constantly!). Is this the lupus you have? Because it goes along with the high PT (prothrombin time). You should be tested for...

Sorry mama....I was hoping for a positive outcome. But, it can still help if you show these to your docs. At least they can see the change then too.

For those of you who are suffering an illness, are undiagnosed and not sure if you have atrophy or any kind of changes....I looked through hundreds of pictures today, to make a collage for my daughter's 16th birthday, and what I found made me feel much better. I fell upon pictures of myself...

I think with ALS it is mostly large muscles, but maybe a PAL will answer that. I do know that with myopathy I get facial twitching. Sometimes it feels like a hook is pulling my lip up!

Oh, how I know your frustration! My opinion is that the docs don't know so they say it's normal twitching. I think normal twitching is the twitching my kids get after a game, or the typical eye twitch that everybody gets. You talk about little pits around your ankles and I was wondering if...

Jenny - it's not for you to just join and tell who should be here or not. I think that would be up to the moderators? Apparently you know nothing about myopathy. The people on here followed my illness for a long time and I was asked to stay. I will repeat poly mimics als.....why can't you...

Rosales - Please don't jump to conclusions....I know it is hard seeing as you are watching someone you love suffer so, but high CPK's along with your other symptoms can be other problems as well. Remember, EMG's can be normal in the other illnesses too. Have you been to a rheumatologist or had...