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I am a 64 yrs. old with no medical insurance. I have gradually had several unexplained physical symptoms of MS since I had a total hip almost two years ago, of course I didn’t immediately suspect MS...I have done a lot of research on every new symptom that would come along these past two years! I g...

Hello, everyone. Due to complications, I am forced to take monoclonal antibodies. I am still to take Aquaporin 4 to see if I'm supposed to be on Nataluzimab or Rituximab. However, both medicines have to come from abroad as I live in the Philippines and is not covered by insurance. Can anyone please ...

Hi everyone! I hope you are all doing well! I’m writing this bc I am an RN and I worked in Urgent Care working 12 + hours three days a week, and I accepted a new job working in outpatient surgery (better hours, pay, and health insurance benefits) I’m nervous bc I am new to working in surgery. Are th...

Hey all, I have just been diagnosed with very early RRMS. It hasn't really affected me physically as of yet but I keep getting adverts on my social media about thinking about life insurance. It is also all targeted at MS. My question to all of you is do you think it is something I should look int...

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Hello everyone, a thought came to me in the dead of last night. Has a diagnosis of MS dramatically affected anyone's car insurance? I presume it has to be declared? Weak legs and twitching eyes are one thing, but if this affects my pocket as well I'll be very unhappy. My car insurance is currently c...

Even people who are good for nothing have the capacity to bring a smile to your face. For instance, when you push them down the stairs.

Can someone help me? I’ve searched the web and all the MS sites and can’t find the answer. I would like to hear from someone who has symptoms daily that come and go. Like everyday. For instance I permanently have numb feet but sometimes in the day it travels up to my knees then goes away back to jus...

Can anyone tell me if Tysabri infusions are free I have been recently been diagnosed with RR MS and will be starting this infusion soon. Are they free if you only have private health insurance 😊

Hi all I'm hoping you can help. I am speaking about 'Patient and Public Involvement' (PPI) at the MS Frontiers conference in Bath, UK on the 5th July. I'm keen to speak with MSers who have been a PPI representative on research projects... is this you? Are you happy to share your experiences? If s...