Looking for
something specific?

I was wondering if anyone here has started on HRT in their mid 40s and found it helped with MS symptoms at all, along with other things (please feel free to share 'other things' if you are comfortable as I have read HRT can help with issues such as loss of libido and with pain and dryness you-know-w...

Dear friends, I'm Pastor Dominique and I was diagnosed with MS relapsing remitting. Among the relapses was numbness of organs, swelling feet and especially double vision. I'm hospitalized now as I'm writing this Post, I have double vision for the 4 time and this took longer than the previous ones b...

Just been diagnosed yesterday with relapsing remitting, think I’m in shock it feels kind of unreal like this all can’t possibly be happening in MY body?. I’ve been told to look over different medications and choose but they all seem to come with side effects …. Do the side effects stop when you are...

I thought I would take a moment to introduce myself! I'm Steph 41, I was diagnosed with relapsing remitting MS in 2006. I moved into a secondary progressive diagnosis in 2015. I am very knowledgeable as such and definitely don't mind helping with suggestions, general information or just a person t...

I was diagnosed in June with RRMS after starting symptoms in Sept 2022. I'm trying to come to terms with my new normal. I'm struggling to return to work after being off since April. Today I went on site and trying to be mindful to not push it I used a mobility scooter for an outdoors meeting (the si...

After reading so many stories of people having to wait so long for a diagnosis, I feel that I must have been very lucky. As I was taken to hospital with a suspected stroke on the 7th of August and diagnosed with RRMS 10th of September. Although I have many old lesions on the MRI results I must have...

I I don’t know if anyone’s dealing with this but thanks to my bladder, memory, balance acting up I haven’t been at work for over 5 months and I don’t have insurance and Medicaid decided me so I can’t go to my appointments and I’m worrying that I will end up relapsing and won’t be able to walk, see, ...

Hi everyone! I’m new here so just saying hi I’ve been offered Mavenclad and not sure what to do, it seems a bit too good to be true Has anyone taken it?? How effective has it been and how are the side effects?? Tnx, Laura

Hello. Been a lot of m9nths since I was here. Back then I was waiting for a 2nd opinion after been told 8 years it was rrms then the last 5 been told I was a hypochondriac. Well, had 2nd opinion, it's definately ms, now spms due to no treatment for 5 years. With other health problems disease modif...

Hi All, I have recently been diagnosed and the neurologist has told me that they’ve referred me to the Ms clinic, but the wait time is 6 months ….. I feel like I’ve very little information about MS (never heard of the disease until I was diagnosed), I don’t know what type of MS I have, how many les...