Search Discussions

Main Content

Treating MS

Are All Essay Writing Services Fake?

Nowadays everyone is looking for essay writing service because there are lots of responsibilities on the student shoulders. Different people have different opinions, so I think this is a pretty subjective question. For me, the most reliable and trustworthy ones are … Read More

CBD oil??*

hi    Just wondering if anyone is using CBD oil?  If so, my Acupincture Physician would like to know what re*****ble source do you get it from and how is dosing done thank Read More


Hi! My husband was given the infusions of Ocrevuz last month and I was wondering if anyone else has started them. I would love to hear others thoughts on the drug and keep in touch about any results. Read More


I've been taking Copxone since late November so I know it hurts, but last night was b-a-d. The past 2 injections (including last night) were leg days. The first one, I used the autoject for and it was more painful, and bled a bit more than my normal. Then last night, I injected the other leg manually thinking… Read More


No matter how much of an organized student you are, you probably had difficulties with writing essays or keeping up with an overload of writing assignments. From time to time, everyone can use some help, so I don’t judge people who use essay writing services.  I’m a huge procrastinator and it brings a lot of… Read More

CBD and THC oil?*

Has anyone found the use of cannabis THC concentrate oil or CBD concentrate oil helpful for MS or spasticity? When I say oil I'm referring to the type made by Rick Simpson. This oil is 95% THC and is black and relatively like toothpaste. Also with the advent of CBD oils becoming legal in all 50 states, they… Read More

Hey it’s me again lol*

Well i Am finally home now ! i have completed my Plasmapheresis treatments & i do feel like they helped a lot with my lesions. The only thing that has been getting me down is my left arm. It's still very weak & with little to no coordination. It's not my dominant arm but it still a challenge getting it back to… Read More


Hi, i was diagnosed 4 months ago with rrms. Just started Vyvanse 6 weeks ago, started at 10, then 20 and doc said 30mg would help. Seems like it was helping me with fatigue and the fuzzy brain at first and now not so much. I was wondering what dose anyone else is taking? Thanks!! Read More

Awful side effects of glatiramer acetate*

Hi all. I’m wondering if anyone had experienced severe body aches/chills/chattering teeth from glatiramer acetate or copaxone. I’ve been on the medication about 6 months and have recently begun having extreme reactions to the medicine. My doctor has not offered me any helpful suggestions on how to prevent… Read More

Pressure in nose and head? Please help*

Hi friends, I see this has been addressed before but several years ago so I wanted to start a new thread. I was diagnosed with MS last week and have been experiencing extreme pressure in the head, behind eyes, nose and ears for months as well as dizzyness that doesn't let up! My neuro and GP are away and I'm… Read More

Ocrevus vs. Tecfidera *

Hello,  I was diagnosed with MS in February 2019. I began taking Gilenya in May but it was not a good fit. Gilenya was causing anxiety on things that I would do on a daily basis. I stopped taking it about a month ago. My MS doctor gave me two options - ocrevus or tecfidera.  Has anyone else taken either… Read More


Hi guys, I'm a high school student researching about MS for an anatomy school project. Recently, I've read and heard from some MS patients about how certain diets can be really helpful with treating MS. I've read about the Best Bet Diet, created by Matt Embry, and it basically describes to stay away from all… Read More

MS medication and sperm count *

Hi ..  So my husband was diagnosed with MS in October 2017. Although we know that MS does not prevent a women getting pregnant or prevent a man from being able to reproduce, I am trying to find out if medication will lower sperm count making it hard to get pregnant. My husband is on gilenya and we were told… Read More

Solumedrol Treatment*

This is the second time I've had to get IV treatment for symptoms. I always get 3 days of treatment using Solumedrol. The first time I got treatment back in October I had little to no symptoms afterwards - only a metallic taste in my mouth and fatigue. This time I have been having extreme hot flashes, burning… Read More

Ampyra causing pain*

Hello I’m new here but have had MS for 10 years. I had 3 spots for most of that time. 1 spot was in the pain & sentivity part of course, so I have Shingle type pain on most of my body. My left side is mimicking the pain on the right so I’m hypersensitive to touch. Cold is extra hellish & if you ever want… Read More

Gilenya *

Hi Guys, I am new to this MS thing!! I was diagnosed in mid Sept and have been on Gilenya for 29 days. I honestly feel worse now before I was on meds. The new thing is lower back pain. It is like a stinging sensation that goes down my left leg. And I am also having neck soreness. Also sensory issues in both… Read More

injection of Brabio pain*

I injected Brabio using the applicator pen into right thigh ( had done this twice before - no symptoms) and immediately had extreme pain shoot down my right outside of thigh. Has continued for a week now, feels like a very sharp - pulling pain extremely painful. GP believes I have injected into nerve. Anyone… Read More

Drugs or no drugs *

Hey Everyone    So this is my first post on any website forum about MS but I figured it might be the best place for suggestions or answers. I visited my neurologist recently and he said as my MRI concerns him that I should consider taking medication for my MS to stop future attacks. Now I'm more of a person… Read More