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@Elsa75 

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Elsa75

Psoriasis

Hi everyone. Apologies that my question is not MS related but as Psoriasis is also an autoimmune condition I'm hoping someone will have some advice. For the least 5 years, my friend has been struggling to get treatment or even get an appointment at the local NHS Trust because her "condition is not ...

Mobilise Carer Support Group.

Good morning folks, hope everyone is keeping well. I have just come across a support group for carers and thought that there may be some here who could benefit from the group. Copy and paste time 😊 https://www.mobiliseonline.co.uk/our-story About Us There are more than 7 million people in the ...

@Jem_Carter 

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Jem_Carter

Can you change your neurologist?

Please let me start off by saying I'm not whining or being ungrateful...my current neurologist has been very efficient in organising scans and treatment over the years. But...I am wondering if I can change my neurologist. When I saw him about a year ago he encouraged me to get back with my ex husban...

@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...