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Hi all, thought I had it sussed this MS after 4 years and permanent symptoms left due to spinal lesson affecting arm and leg sensation. Lockdown has seriously challenged me and deconditioned me, body now reacting. How do you pick yourself up and dust yourself down and stay positive! New treatment ch...

X700 Granite Male Enhancement is another male upgrade item that encourages an individual to increase enough number of s3xual hormones in the body. This item is useful in expelling all the s3xual issues from the body. One can without much of a stretch ready to evacuate the shorter erection and low ch...

So I was diagnosed with MS in 2018 by a general neurologist after all the tests and on and off symptoms for years, I have 5 lesions on brain 1 on the spine, since then been with a MS specialist who did not want to put me on disease modifying drugs as he wanted to watch me further he believes it's M...

Hiya everyone 🙂 I have a lumber MRI this Thurs and I have been having symptoms again since May 2020. My symptoms started in May 2019 numb feet, pins and needles, ataxia and weakness on left side. I have brain fog, cant concentrate and struggle finding the right words. I was seen in Nov 19 by a ...

Hi, first time I have posted but am having tough day. Am 50 but don’t like to think I look it or feel it, in my head at least. Diagnosed rrms in Jan this year (2020). It was actually good to have reason for so many things gone wrong with my health over many years. Am generally not too bad, bladder ...

good afternoon everyone it's been a while since I last posted anything! My neurologist didn't give me anything new to help my ms she still prescribed me copaxone and she said to stop taking it for a few months and then start taking it again! Since I stopped taking it I have been feeling great having...

What does everyone use to keep cool and to keep body temperature down when out and about and walking my symptoms flare up when out a walk and speaking to my nurse she reckons its due to my temperature going up my eyes go so blurry and drop foot gets worse goes away completely after cooling down

Hi I have been diagnosed with RRMS a couple of weeks ago. I am 41 and it would seem that I have had MS for years, although I haven’t been aware of symptoms until April. My MS is very active with a lot of inflammation. I have been recommended cladribine, which seems very good and not intrusive. I jus...

I have been using fingolimod almost 18 months and recently l have been constantly ill, flue, coughing and others and in the last couple of months a scaly, itchy lesion or patch appeared on the outside of my right arm which does not seem to be healing and fits with the descriptions of skin cancer tha...

Hello people I am a little new at this posting questions. But I thought I’d give it a go. Who better to ask than the ma community. I was diagnosed with ms after having optic neuritis About 8-9 years ago. Since then I have very few symptoms. I do suffer what I Describe as a ice cold feeling/ pain ...