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@martinkelly 

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martinkelly

ppms treatments

I was diagnosed in 2012/2013 , but have had symptoms for 15 years or so. I'm on Fampyra and Lyrica which seem to help. Magnesium and Lecithin very important too. I am in Germany at the moment where the treatment is amazing compared to Ireland where I am from. Anyone else out there with questions on...

@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...

@Alessa_Bless 

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Alessa_Bless

The natural route

Hey there... New to this... I’m wanting to hear feed back from folks who have opted out of DMT... I was diagnosed 7 months after my son was born in 2010. I am currently having my 3rd relapse, though this one has required a 3 day dose of solumedrol. I completely changed my lifestyle after diagnosis, ...

@schulz_alice 

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schulz_alice

Health is wealth those with MS

Never meet a group of people that are not updated on new discoveries and cures.I posted a message here to help but it was removed because admin claimed i broke house rules..How am i suppose to help other patients in the community when i can not direct them where to get a cure???If you are still with...

@Cooper 

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Cooper

Cognitive issues............

I was diagnosed last year, i thought I was lucky with relatively light physical symptoms. Balance, some pain but cognitive problems are really starting again.............. Does anyone have issues of trying to make simple calculations work in your head? I find it difficult at the moment. I'm trying t...

@Tishilliams 

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Tishilliams

Likeminded friends

Hey Guys🤸🏾‍♂️ Im hoping to meet any females, late 30s, mothers. Who are driven with the belief that Dis-Ease can be cured holistical, through diet, mindset and life style. And are currently not relying on prescribed Pharmaceuticals. I am not discriminating im just hoping to connect with likeminded...

@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...

@Emma_Byers 

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Emma_Byers

Face and head pain

Sorry long post!! Finally got a diagnosis in March this year. Been a long haul from 2013. In the last 4 days I've had excruciating pain in my face and a banging headache. Back in 2013 it was optic neuritis I was diagnosed with but I ended up with more symptoms and everything got worse over the years...

@Jen4s 

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Jen4s

Ocrevus

Morning! I was due to start Ocrevus but this has been put on hold due to the current pandemic. I’m currently waiting to commence tysabri instead. Just wondering if anyone else is in the same situation? I had been on Copaxone but the injections were leaving craters all over me and between the burnin...

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...