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Treating MS


New to Nuedexta I have just been put on Nuedexta, for MS of course but not really sure what is being targeted Neuro said it will supress spontaneous laughing and crying, which I do not have. Also will help with depression and cognitive problems, which I also think I do not have too much problem with. To add… Read More


OK. So I do not normally contribute to blogs, discussion, conversations etc. as I fall firmly into the "lurker" category. However, I do check out this site often and have appreciated everyone else's contributions. So why contribute now?  The reason I am typing now is in about 4hrs I am going for my first… Read More

What to Eat?*

I was given a pre diagnosis/ beginning stages diagnosis. They'll be keeping an eye on the foci.  Anyways, I am looking at using diet to treat it until my next appointment.  I don't know which would be best. The Wahls, OMS Diet or if there is another diet? I am a type 2 diabetic. I control it with diet . I'm… Read More


Why should I take Ampyra is my balance and coordinaiton are already very unstable?  Two of the side effects are dizziness and impaired balance.  When I asked my specialist what could help with wlking, he suggested Ampyra knowing I have extreme balance and coordination issues.  We also talked about an AFO for… Read More

Injections of Copaxone*

I have recently started copaxone. I take 40 mg injections three times a weeks. I have plenty of "fleshy" places everywhere that I am supposed to inject except on my hips. If I pinch up insert the needle and release the needle will pull right out. Any suggestions on how to give yourself shots in your hips when… Read More

Aubagio / Tecfidera*

Hey everyone! So with some good news from my neurologist about my lesions and their location, we are hoping this doesnt ever get aggresive God willing, and from a medical stand point. With that being said I have been leaning more towards the treatment of my RRMS with pills before I go right for an inejction… Read More

Immediate post injection reaction*

Yesterday was my shot day. I have been on copaxone 40mg 3/xweek for 1.5 years now. I gave the shot in my right stomach and within seconds, my face was flushed and warm, my chest got tight with heart palpitaions, my lips were itchy, and the whole lower half of my right abdomen was swollen around the injection… Read More


hello to everybody, I live in Italy and ms primary from 2008; I have read that someone with ms uses walkaid that is an eltctrosimulator helping against footdrop; is there anyone who knows about it; here in Italy nobody uses it. I thank you in advance best regards Anna Read More

baclofen pump

My Dr. has recommended a baclofen pump. I went to hospital for a 3 day test to see if it would work for me. My Dr. thought it was successful and that it would be of benefit to me. I would like to hear from others that have the pump and get their opinions about how it works for them, how difficult or easy it was… Read More

Cannabis Oil*

Hi everyone... my twin sister was diagnosed with the progressive form of MS and I was wondering if anyone has used or heard of "cannabis oil" as a side treatment along with tecfledura and amantadine? Are there any contra-indications using these medicines along with the cannabis oil?  I would so appreciate an… Read More

Hemp Oil*

Anyone using hemp oil?  ​You who are using pot, have you noticed a consistent benefit or varying? Are you using a single strain or varying the type of pot you are using? ​For six months now I have been on hemp oil and have noticed an improvement in the use of my hands and arms, so much so that  the other dayI… Read More


Hello! I started my daily injections of copaxone last week and am feeling so much better than I have felt in months. Does it usually work this fast? How will I know if its slowing down the progression? I welcome any comments and or suggestions Thanks! Read More


So I'm kinda freaking out right now. I take two 240mg pills a day. One at 9am and the second 9pm. At around 11:40ish I accidentally took another pill. I had meant to take my other medicine. Has anyone ever done this before? Any did effects? Should I be very concern or am I freaking out over nothing? Read More

Your favorite treatment options?*

I was diagnosed with RRMS in Dec. 2017. I am now approaching the meeting with my neurologist about treatment options, etc. I have a choice of pills and injections. We are all so different so I know two people aren’t alike but I am looking to hear what people like or dislike about either or. All of the side… Read More


I am looking for anyone who has been treated with Cytoxan (chemo). I am scheduled to start it on Feb. 14. I started Rituxan in November and I have had a worsening of symptoms. I'd like to hear about your personal experience with the Cytoxan. Thank you.   Read More