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Hi! my name is Kim. I have had MS since 2013. Looking for some insight on how to live healthy with MS. If anyone can give me advise on who to talk to get to be healthy and what to eat and what exercises should be done.

Hey All!! Im new to this App i have only recently branched out to find out more about MS and healthy living. I got diagnosed with MS when i was 13 years old i am now 25. I went threw all of school not talking about my ms i talk to nobody as it was a rollercoaster getting diagnosed with Ms and findin...

I heard that cutting down on/cutting meat out of your diet can slow the progression of MS. Has anyone found that it's helped their symptoms at all please? Legit willing to try anything at the moment 😂🤞🏻 #diet #healthyliving #meatfree #rrms

My experience of using cannabis as an alternative to using prescribed drugs to aid my MS symptoms. Having been diagnosed with Multiple Sclerosis in April 2004, I have gone through Relapsing Remitting (RRMS), Secondary Progressive (SPMS) and now for the past couple of years find myself at the Prim...

So…. I saw the neuro and have just received ‘the letter’. It says… “Possible sensory cervical transverse myelitis? …demyelination. I am awaiting an appointment for MRI’s on brain and c spine. Most of the tests he carried out seemed to not turn up any negative results. It says that the lower limb exa...

Morning all! Hope you are well. So as u may or may not know I am a qualified nutritionist. I have set up my own website and work at 2 clinics in London. I do also do skype consultations. Diet and healthy living is extremely important for everyone but especially when you have a condition like ours. A...

Hello folks, At Christmas there i got talking to a physio in a social setting who started telling me about these pills she had access too that had helped MS patients she worked with. I didn't think much of it until i was invited to a group all with other patients and the 'expert' - upon googling a...

I have MS. 13 Years strong no episodes in 9 years. I'm fatigue usually. I drink coffee it helps but then it kicks my ass and I'm in bed by 9 :)

Hello everyone! Mother of 4 here. I was diagnosed with MS in 2020 at the beginning of the Covid shit down. That was a wild ride! I was 4 months postpartum when I experienced the worse relapse I’ve ever had. It’s been a journey and I’m still finding my way. I start ocrevus at the end of April hopeful...

Hi all!! Just a question I’m feeling awful at the moment and all new to ms, haven’t started treatment yet as, still don’t know what ms I have , I see my neurologist on the 25th april, I’m absolutely shattered, my vision is rough, can’t walk properly and tingling in my arms, is this what you call an ...

God dose miracles . But this disease is going to keep getting worse everyday I wonder if I get up if I'm going to be able to walk this isn't like the flu it don't just go away I have it for the rest of my life ..🥴 I'm on ocrevus life has went down hill for the last few years I have vision prob...

Hey there MSers 👋 What kind of diet do you follow? I recently came across some exciting news that I just had to share with you. You might be interested in hearing about a study that suggests a Mediterranean diet could reduce the risk of cognitive problems, like memory and thinking skills. The stu...

Hello everyone 😊 Just a question, have you heard of The Molii Suit ? If yes ,is it effective?

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In this episode of MSers React Dave, Roxy, Katt and Heather respond to posts on Shift.ms about loneliness. Have you experienced loneliness because of your MS? If so you’re not alone! If you have an experience to share, or a way that you’ve learnt to adapt then please share your story in the comment...

Hey🤍 My Baby Boy was born 2 weeks ago. I didnt do any medication during pregnancy, now my neurologist recommended me to start tysabri as the rebound risk after giving birth is very high. I am breastfeeding (which is also a kind of natural protection) and I love breastfeeding so much! According to m...

Hi thera Im reaching out to see if there are any msers in Derbyshire/ Chesterfield, my family and friends are great but only someone with ms will understand the lonliness and despair that this brings. Would love to chat and vent! Yours in hope xx

Hi it’s hilary. My brother has been diagnosed with ms in November last year. Very bad system here nobody taking it seriously. He has continued to degress he has slowed down his work load. Now he went to Spain to get a second opinion which now shown to have gone from remitting. And relapsing to PPMS....

“My neurologist said, you've got MS. I remember walking out of the appointment and just sort of, not believing it.” 💚 This week's episode is with the inspiring @Sarahemily who reveals what it was like to have her confidence knocked by MS. Has MS knocked your confidence at all? Share your story i...

Anyone gone cold turkey on meds and decided to try a more natural approach to treating their MS? Just curious what people's experiences were. Thanks!