Copaxone secondary progressive ms

Common Questions and Answers about Copaxone secondary progressive ms

copaxone

494976 tn?1302710701 Anyone here had any of the chemo therapies to treat secondary progressive ms or any other progressive types of ms? Such as Azathioprine,Cyclophoshamide,Cyclosporine,Methotrexate or Mitoxantrone? I would be interested in hearing how people have responded to these therapies and if they helped delay progression at all or improved any symptoms. Are there any other chemo therapies I have not mentioned above used in the treatment of ms? Aimee.
494976 tn?1302710701 If after many years of frequent relapses you find yourself not having any anymore, for say two years, with some problems but not dramatically worsening, could this be secondary progressive MS? Or is it possible for relapses to become less frequent? Are there any signs to look out for that it may be turning into secondary progressive MS? What good treatments are available ( In UK)? Are there any new medications been trialed? Sorry for all the questions.
Avatar n tn Various sleep disorders are very common in those with ms. Often ms fatigue is secondary to something that might be treatable. Hope this helps!!
1168718 tn?1464983535 Hi my fellow MSers ....... Sorry I have been absent quite a bit, but have been dealing with alot of stuff. Mainly Dr. related, but also some complicated family issues. Life can be so very difficult sometimes, but we still have to somehow rise up and smile anyways, as the sun is still shining. I have been missing my 4 grand children so very much, and we have had NO communication from DIL or our son.
Avatar m tn Hi Grewy - For me, Secondary Progressive MS (SMSP) is just a label. What matters is how you are doing. My initial diagnosis was SPMS. I had a major relapse in July of 2011. Prior to that MS was not something I'd ever thought about. We did a little health/symptom archeology and it turns out my first relapse had been 20 years before. I was not suffering in the intervening years, nor was I looking for any kind of diagnosis. I still get up everyday and go to work.
Avatar f tn My initial diagnosis was Secondary Progressive MS. When I was idagnosed 3 1/2 years ago my doc though I was already beyond the reach of the CRAB's. My first DMD as Tysabri. I was on it for 20 months before it stopped working. I then switched to Rituxan. Tecfidera is "stronger" than the CRAB's, but not as strong as Tysabri. I'm not sure here Aubagio and Gilenya fit on the strength scale, but I would ask your neuro about them. They are both oral meds.
Avatar f tn By the time I figured out that I have MS, mine had moved from RRMS to secondary progressive MS. This means I may still have relapses, but some of my symptoms are around for keeps. Were you told what flavor yours is?
Avatar f tn Besides, they showed me lesions on an MRI from 19 years earlier so I figured this was now Secondary Progressive MS anyway. No use for a DMD there, right? Fast forward...... I ended up giving Copaxone a try because I can never say something doesn't work for me unless I've tried it. By the end of the first year of daily injections I was feeling better than I had in many years. I did NOT return to anything close to a pre-MS condition.
1448980 tn?1284751989 You either start with Relapsing Remitting MS 85% of people with MS or Primary Progressive MS 10% of people with MS. Then people with RRMS at some point may go into Secondary Progressive or in rare cases Secondary relapsing MS. PPMS is not strong and rapid in all cases it just is different from RRMS. It takes longer to diagnose because it is subtle. I have had PPMS they say for over forty years and I am still in pretty good shape.
15038840 tn?1438115670 Hello.I take chance from your post to ask you and anybody else: Do you believe that meds help in progression of the disease? Why neurologists advertise them with so much certainty? When i see that patients, on 20 average years after the diagnosis start to have problems, how can I believe the doctors? For me, they lie!!! Foolness, interests? I don't know. ''Take meds, otherwise you'll be on a whellchair!'' Bullishits!
867582 tn?1311627397 s distressing news regarding her new progressive MS diagnosis, I began to wonder how many others here have progressive MS and how many have relapsing/remitting and invite you to participate in a survey. This question is for both, those diagnosed with MS and for Limbolanders (based on your age and symptoms what type of MS do you THINK you have?). Based on my symptoms, I feel I have Progressive Relapsing.
Avatar m tn Fingolimod (Gilenya) and Mitoxantrone are very different therapies, the latter more common as a treatment for secondary progressive MS. Gilenya is prescribed for relapsing-remitting MS. From your limited description of current symptoms, with no historical perspective, I would guess your sister is secondary progressive. But it's only a guess. Perhaps that's why the four earlier treatments failed, because they are for relapsing-remitting.
Avatar f tn A significant number of people with Relapsing/remitting MS move on to Secondary progressive MS. In secondary progressive MS there are less likely to be relapses. There is a steady advancing of the disease. In my case, thankfully, the advancing is taking its sweet time :-) The other 2 types of MS are progressive relapsing and primary progressive. These are distinct types of MS. They occur less frequently and tend to be more severe.