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@MSRN 

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MSRN

Greetings! New to this site

Hello I am new to this site and hope to make some connections with others with multiple sclerosis. Hope to be helpful to others. All best

@JoyceG. 

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JoyceG.

No DMT at the moment...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

@schulz_alice 

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schulz_alice

Multiple Sclerosis cure

My name is SCHULZ ALICE and i am 46 years old . I was born on 19/01/1974 in Carinthia (Klagenfurt)Austria . I grew up there till the age of 20 when i started having Vision problems,Fatigue and weakness,Bladder and bowel dysfunction,Sexual dysfunction,Cognitive problems. Since i was still young i nev...

@prianka 

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prianka

GP wont listen. Undiagnosed..

Hi All; I am new to the forum and i will be honest in that i have a problem speaking to my GPs due to neglect in the past which lost me my first born.. I have strong symptoms of MS and dared to mention it to 2 diferent GPs but was fobbed of,especially when i mentioned the heat intollerance; all i go...

@Thorpee 

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Thorpee

Hello, I'm new here..

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

@carolelawrence 

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carolelawrence

Not happy!

Long story..had mri Feb 2 non specific liasions on my brain and 2 non specific liasions on spine. My left leg and foot numb since Jan. My right leg and foot and my right toes numb last 4 weeks..so my mobilty gradually deteriorating last 14months..dreadful burning night pain in legs and feet burning ...

@BULLMAN 

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BULLMAN

Humour 36

Have you heard about the new restaurant called ‘Karma?’ There’s no menu—you get what you deserve

@DominicS 

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DominicS

Can you help Prof G? Got MS, Had Covid?

He says, "I am interested to know if any of you who have COVID-19 are suffering from a persistent loss of smell and taste and how has it affected your life? Please let us know if smell training makes a difference." - Here is the full post: https://multiple-sclerosis-research.org/2020/06/mscovid19-lo...

Diet

Hi all, Can anybody recommend a diet they feel is helping? I read/see a lot of different things, basically most just recommend cutting out all the so called bad things we westerners eat, days,meat etc ??? I have had some recent issues with having a few items cooked in fat! Stomach aches etc and...

Undiagnosed Think i have MS

Hi; only just joined and hope i am doing this right folks..I am undiagnosed. I have mentioned twice to GPs that i am sure i have MS but they brushed it off saying such as,MS sufferers dont have problems with heat like i do so i want s to see a private Neurologist but i still need a referral letter o...