May
13
Progressive Multiple Sclerosis
Posted by admin Comments (12)
Isobel Scarisbrick, Ph.D., describes a new Mayo Clinic study that found two particular enzymes were elevated in patients with progressive multiple sclerosis. These findings give researchers new hope for developing a therapy for progressive multiple sclerosis.
Categories: Multiple Sclerosis Early Symptoms
Interesting video for a guy that was dignosed with M.S. I am interested in the stem cell therapy, so keep me posted.
She is a great PI, and does great work. If there is anyone who can find the answers it would be her!
Wow! Someone who talks about progressive MS! None of the Neurotrons here seem to have even heard of such a thing, and dismiss those of us who have it as lazy or as malingerers. Then again, the Neuros here don’t like to diagnose MS even if all three tests major accepted tests come back positive. Once when I was having a nasty exaserbation one of the Pakistani Neuros prescribed yogurt! LOL! YOGURT!!! Well, I ate my yogurt and nothing changed, but at least he was happy.
Well, isn’t that the disease that cellist Jacqueline Du Pre had?
I would suggest focusing on lowered endorphin levels in lab rats and those studied before and after the use of Low Dose Naltrexone.
Please keep up this research!!!!!!!!
good grief!
I absolutely agree- nobody seems to know or care about we people with progressive MS. All the drugs etc are always for people with R/R MS.
The problem is all in the numbers. Drug companies research and manufacture drugs which will bring them the largest profits(though to be fair,they do provide money and resources for research which won’t bring in a rusty penny if it will help a large number of people).Those of us with progressive MS are a very small subset of a disease which is itself considered rare(don’t you feel special?)So the drug companies aren’t interested.Our best hope lays with researchers like the one in this video.
I am so glad that you are woking on studying progressive MS! Thank you for doing this!
Hugs,
Angela
Thanks. Progressives don’t get the attention they desperately need. I was diagnosed in Oct. 2009 and I’m rapidly progressing. If the Mayo Clinic in the Phoenix area has a need for any research subjects, I would love to volunteer.
I have been secondary progressive for about 4 years after being relapsing remitting for 14 years. Please keep studying the progressive forms of MS so that we can have hope, too!
Thank you!
please kkep up the good work to bring hope for all those who live with this terrible disease