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I've got an 8 month old that won't sleep for longer than 90minutes in a row (usually 30 max!), I've had a cold/flu for the last 3 weeks (it's developed with different symptoms so I don't know if it's actually different illnesses), I'm back at work after maternity leave and my heads in bits, and also...

I was diagnosed with RRMS in 2022. It’s been a journey in trying to educate myself and people close to me about MS. I wrote a blog post last week that friends tell me gave them a better insight into and understanding of MS. This isn’t a sales pitch, I understand hypnotherapy isn’t for everyone. Bu...

Ever since my diagnosis, things just went down hill. I wake up in pain, I can’t walk, can’t work.And I’m alone. No family no friends and my m embarrassed to be seen n public self esteem gone. I’m trying to handle it but it gets harder every day.

Hello, I’m new here. I’m Susana, I was diagnosed in June 2024. During the last months I’ve been medicated to anxiety and, of course, having therapy. But, even I have support from my family, it’s a very lonely road where sometimes I’m ok, or even happy, and other times I just want cry and give up. I’...

🦃Have a very happy Thanksgiving from my family to yours

Has anybody found people's attitudes toward you changing post diagnosis. Even my family seem unsympathetic. I feel like a nuisance and a burden and a downer to others. Is this really common with fellow MS sufferers?

Hi I'm Alexis. I'm 39. Was diagnosed with remitting relaosing multiple sclerosis five years ago and it's come in and destroyed my world. No one in my family or my friends circle gets me anymore. They said I've changed 🙄

I've been swimming down that river called denial. I was diagnosed in March. And not coping very well. Only my boss and a work bestie knows of my diagnosis. My family don't check in on me since they were told, my two friends i do have don't even ask about it anymore. My partner doesn't seem to a...