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robynmich
Excluding medications, what treatments help the most?*

Hi guys! I'm new here and hoping to be recommended some natural treatments to pair with my prescription. Any recommendations? I'm curious about yoga, massage, acupuncture etc.. I'm very stiff…

6 Replies

463 Views

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msfish
MS and a Familys Death*

A Grandma with MS and a Family Death      Today is October 9th. October 7th was my grandson's birthday. He passed away June 30th at 1:40pm. He would have been five years old. He was a very…

2 Replies

545 Views

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thisiscrazy
High dose steroids*

My MS story has been random.  My symptoms and opportunities were many but mostly put off because I thought they were in my head.  I was diagnosed after a car wreck because I had trigeminal…

5 Replies

421 Views

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frederick86
Aubagio and Low Dose Naltrexone *

Is there any who is taking or has taken both Aubagio and Low Dose Naltrexone at the same time?  Was that successful for you?

1 Replies

436 Views

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echobird
Family still at it! They are still trying to drive me insane *

So my family is still at it trying to drive me insane! I have tried so hard but they don't give a damn. They are still intent on trying to push me over the edge and get me to mess up. Then my…

1 Replies

257 Views

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beckyfen
Signs of MS *

hi, about 3 years ago my partner had optic neuritis and was treated for it at the time they queried ms but he had no other symptoms so it wasn’t taken any further. Since then he got very mild…

2 Replies

517 Views

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sls120162
Things I want to do, but my MS gets in the way *

For example, I am trying to clean house, but my legs of course don't work like they used to.  I hurt so bad I just want to sit.  I was in a STEP program but I quit because I could not even…

4 Replies

234 Views

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red100
Gaming helps MS in lots of ways. *

Hello All, I am new here, and somewhat newly diagnosed with MS (Summer 2018) I don't know why I didn't think of joining communities sooner, but better late than never right!?  The main…

1 Replies

286 Views

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breannamariedesign
Ms Society Fundraiser! *

Hey everyone! I wanted to share a fundraiser I'm putting on that is very dear to my heart.   This summer my boyfriend, Ian Dyer, passed away unexpectedly.   Ian's mother Kim was diagnosed…

1 Replies

597 Views

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jkg
Option for Health insurance in US *

My daughter wish to do higher studies in US. She was dignosed with MS in 2016 and generally doing well with medications in India with no disability at all. If she starts studying in US, can…

1 Replies

618 Views

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adr810
MS and Crohn’s Disease *

Hello! I’ve had Crohn’s disease for 14 years and I have been on immunosuppressant drugs for the last 5 years. In winter 2016 I started having numbness from my waist down. In summer 2017 I had…

2 Replies

570 Views

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DeeDee
Autoimmune Diet*

Hi! My hormone doctor (not my MS doctor) has insisted that I follow the very restrictive AIP diet, (autoimmune diet). She swears that most foods are attacking my gut and making my MS worse…

11 Replies

632 Views

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jenlric
Drugs or no drugs *

Hey Everyone    So this is my first post on any website forum about MS but I figured it might be the best place for suggestions or answers. I visited my neurologist recently and he said as my…

9 Replies

669 Views

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dimple2
Hi*

I am new here, i would like to hear anyone who had the same symptoms. I had this for like 3years but at first i only felt little like electric shocked running from my left foot up to my hip…

2 Replies

539 Views

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maria1
Dear arielfriar*

 Your situation has me overwhelmed, my brain is searching for what I would do in your situation, who to call for help, what kid of help is immediate and possible? Without family or friends to…

6 Replies

227 Views

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pacific26
Need help with care problem*

Hello Everyone,I want the public to know what is happening to me and this is in the public interest:I have MS and I am physically disabled living in Vancouver BC and I feel that my health and…

3 Replies

298 Views

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mblanco
Have you experienced these symptoms?*

Hey everyone. My name is Melissa, I’m 33, a teacher, and living in California. I am not currently diagnosed with MS, but my symptoms are pretty concerning. Please let me know if you’ve…

5 Replies

497 Views

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Kris-MSConnection
Your Opinion Matters*

Update: Survey is now closed.  Thank you!We believe that people affected by MS live better lives when they're connected. To help us provide you with the best resources, support and information…

4 Replies

505 Views

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Kris-MSConnection
Pathways to a Cure - Facebook Live*

Join Us! The National MS Society is hosting a live Facebook event Thursday, September 26 called Pathways to a Cure from 2-3pm ET. More info here: [url=https://secure.nationalmssociety.org…

1 Replies

310 Views

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lunastarr
M.S. Yoga*

Hello Everyone! My name is Luna and I am part of starting a yoga class engineered for people with Multiple Sclerosis and any other disability that limits mobility.  As for right now I am…

0 Replies

416 Views

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