therapy

I have looked into this study and had a fairly extensive discussion with the study coordinator at the San Francisco site. I am posting information about this study here in case anyone is interested. Enrollment is still open for this phase 3 study. The study is sponsored by Brainstorm Cell...

I've been exploring adjunct therapies for the pain I experience. I get a lot of joint pain from tendonitis and torn rotator cuffs. So far PT has only made it worse. I came across one PT who uses pulsed electromagnetic field therapy in conjunction with her hands-on approach to PT. She has...

Should ALS patient do physical exercise for therapy? Some say no and save energy for things that lend to quality of life. Some say only range of motion. Some posts from PALS say It helps maintains muscle tone.. My wife still has the ability to lift herself into a standing position which...

Hello everyone , nice to meet you guys! Anyways my mom has als , as far a son we know it's not familial , however over the last two months I've had some really weird symptoms , it started with my bicep spasming out on my right arm for about a minute , ever since my bicep has felt sore and tired...

Anyone familiar with this treatment for excess saliva?

I’ve been with my partner for almost five years but we don’t live together and don’t plan too. Only a few months ago I experienced the sudden unexpected death, by fentynol, of my eighteen year old daughter. I’m still trying to cope with that. My partner has always been unable to be supportive...

Did anyone prove any cell therapy? If so, could you please share your ecperience? I am thinking of taking the Wu Medical Center therapy but I would like to hear about some PALS that had an experience on it. many thanks. Bests

You now have me worried that I may have brought on ALS earlier. Pulsed Electromagnetic Fields: How They Heal | The Dr. Oz Show I was taking MPF therapy before I was diagnosed with ALS.....Could it have caused more damage, since it made muscles jump! 3 days per week for 9 weeks!

Good morning, I'm new to this forum as a member, but have reading you for a while and know enough to be really scared. I am female of 32 years old, with neuro symptoms for two and a half years. Since than I have been to two neuromuscular neurologist several times. Prior these symptoms ( 9...

in a 750000 citizens capital of my country, i found just one guy (early twenties) who has ALS. he was in china, hardly speaking and moving etc so i dont have base to compare with him. there are at least more than 15 people having ALS in my town, but for sure they dont use internet. as i said...