Because of the heatwaves in the UK my fatigue has been awful but I've noticed that after eating I slump so much it's a little bit sad and scary. I ate out today with friends and it was me who was driving every one and I had to come home by 6pm. Id been out three hours. I'm a grown woman and my batte...

Where are you joining from while living with Multiple Sclerosis? 🌍

Bit concerned. I've developed some completely new symptoms and I'm not sure whether I should contact my MS nurse. 🧠 My IQ has increased by about 20%. 🧹 I've suddenly become ridiculously organised and tidy. I now put things back where they actually belong. 📸 Developed a photographic memory. I c...

Feels like I’m a horrible person as I hate ppl who are annoying!!! But I get along with people who are nice to me 😁. Them annoying people are part of the family and feel like I can’t talk to them anymore!!! Hate feeling like this as it makes me ☹️. I haven’t got friends my age anymore as they all m...

I just found out I have to stay away from seed oils, dairy, artificial sugar and gluten. Sadly I have banned myself from takeaways when im felling lazy, I have a premade meal from 'Field Doctor' Thankfully they help with dairy free, gluten free and high protein. Plus they cook with olive 🫒 oil. ...

I've been dealing with MS since 2010 ( Drs said ive had it longer). Left side of body is no longer useful. Left leg, I wear a brace because my leg doesn't work. Neuropathy on entire left side of body even face. Now I'm starting to feel neuropathy creeping on my good side right side right foot. Went...

Does anyone else take ashwaganda? It's improved some of my symptoms & boy has it helped my anxiety! It's been my favorite thing I've found to help me ms this far. Any other things that help yours?

I don't want to trigger a type 2 diabetes side effect. Google says: High sugar consumption 🍦🥤🧋🧃🧉can worsen multiple sclerosis (MS) symptoms and accelerate disease progression. Diets high in refined sugars promote systemic inflammation, trigger severe energy crashes that exacerbate MS-related fa...

I’ve had MS officially for 20 months now and started Kesimpta 16 months ago. I got results from my second MRI since starting treatment and pleased to say they noticed no significant changes. I’m very happy about this and proud of myself because although the treatment is a big factor, I believe my he...