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Hi, similar to my post yesterday. I’m trying to figure out the best medication and was just curious if any of you have tried Copaxone? If you have did it prove to work or not at all??

Howdy all, I'm new to this site after my MS nurse pointed me in this direction. A little about me: I'm a 34 year old Male. Married with a young son, 7 months old. I Live in Southampton. I enjoy paddle boarding, going out on my mountain bike. I did enjoy the gym but haven't really been since Aug 2...

Well still waiting for appointment neurologist..my left leg been numb since January..so my mobility has got worse but yesterday I woke to find my right leg too is going numb! Toes been numb weeks but it's lower leg it's creeping in too now. I've still been ok till today to get up stairs steadily..bu...

Over the past 15 years or so I have taken a host of drugs (ending with ‘in’) without success. Even the last course of lidocaine infusions failed to have the same affect that they originally did. The pain management consultant informed me that the only other way to go was Morphine patches. My GP was...

<p>My 14 month old granddaughter lives with us (along with her parents) plus my other sons. 2 are mental health key workers, my daughter in law is a nursery nurse key worker (currently furloughed) and my youngest at uni is earning money working part time as a key worker in Farmfoods frozen food shop...</p>

<p>Is it safe for someone with PPMS to holiday in Devon UK this July .. We are prepared to follow all the rules given out by the government. I know MS means a compromised immune system but not sure if MS is on the vulnerable list ?</p> <p>Thank You<br> Jenny </p> <div class="i-support-link"> &lt;...</div>

<p>Hi,</p> <p>I just had my latest infusion of Rituxan (after a COVID delay), and I always feel terrible afterward, but I’ve heard people say they feel better after treatment. Is this a case of “no two the same,” because of different DMTs, a combo? Just curious as I sit here in my post-infusion blah...</p>

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<p>Need some advice. I have had health issues half my life. First started when I was about 16. I’ve been trying to find answers for years. Just recently found out that Ms was put in my medical records 2 years ago, although the Dr never verbally told me this. I also have trigeminal, occipital a...</p>

Sorry long post!! Finally got a diagnosis in March this year. Been a long haul from 2013. In the last 4 days I've had excruciating pain in my face and a banging headache. Back in 2013 it was optic neuritis I was diagnosed with but I ended up with more symptoms and everything got worse over the years...