Multiple Sclerosis

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5 medium

Aspirins new study

Aspirin Suppresses MS Symptoms by Preventing Loss of Regulatory T-cells, Mouse Study Shows
DECEMBER 5, 2018 Patricia Inacio, PhDBY PATRICIA INACIO, PHD IN NEWS.
Aspirin Suppresses MS Symptoms by Preventing Loss of Regulatory T-cells, Mouse Study Shows
Aspirin, administered orally at low doses, was sufficient to suppress multiple sclerosis (MS) symptoms in a mouse model of relapsing-remitting MS (RRMS) and chronic MS, a study reports.

The clinical benefits of aspirin were linked to an increase… read more

posted 4 days ago
A MyMSTeam Member said:

I take Bayer 81mg low dose for my heart had no effect on my MS.

posted about 1 hour ago
6 medium

Droo foot and Ottobock

Hey everone do any of you wear a AFO brace for drop foot? If so, does anyone wear the Ottobock brand? I’m curious if any has drop foot and wears a brace if they can only wear sneakers!? I get my brace on the 21st and i am very anxous to get the brace and would love to hear others experiences!

edited, originally posted 1 day ago
A MyMSTeam Member said:

I've always just worn tennis shoes because I have had a stroke in march along with MS. So because of the stroke/MS I have perminit drop foot!!

posted about 2 hours ago
3 medium

Vent 101

Not really a question but someone too vent to whom understands my frustration! Symptoms that never go away, and most days seem to worsen. No obvious new ones that stay around, however, intermittently rear their head. New MRI's are stable, yet i still feel like i'm slipping! I get so frustrated with doctor's! I don't understand completely this dredful disease, and i have to deal with every issue that arises! Sure when my annual MRI's come back stable, i feel like i should be thankful and relieved, but… read more

posted 13 days ago
A MyMSTeam Member said:

It's good to vent. I'm so sorry that you are not feeling well. Try (I know it's hard) to stay positive and not dwell on your frustrations after the… read more

posted about 2 hours ago
3 medium

Do you miss the person you were before MS?

posted about 1 year ago
A MyMSTeam Member said:

Yes I do, but I deal with what I have now :-)

posted about 2 hours ago
0 medium

Has anyone heard about stem cells therapy. I want to know if anyone has tried it and if it has a risk?

posted 3 days ago
A MyMSTeam Member said:

A slippery slope and the admission fee is $65,000.00 minimum to start.

posted about 2 hours ago
1 medium

Does anyone else forget their words?

I have words just disappear from my head. A typical sentence is like " I got up to answer the....the thing where u go in and out of the house. That thing. God what is it called! " oh yeah. It's a door. Lose words like that. All the time. I get so frustrated! Its like charades with my life! Am I the only one?

posted 10 days ago
A MyMSTeam Member said:

Not to worry @A MyMSTeam Member you are not alone. I do that forgetting what it's called or saying the wrong thing and having my husband or son look at… read more

posted 5 days ago
3 medium

Has your relationship been negatively impacted by the moods/ mindset /frustration of MS?

How has your relationship been affected? I have a hard time telling the difference from what is just being "moody" because I feel terrible , and what isn't. My spouse just thinks im a jerk all the time now.

posted almost 2 years ago
A MyMSTeam Member said:

I am on the other side of ms, meaning I have had it 25 years, and all those fears and things I worried about have come to pass. Yes, it affected my… read more

posted about 4 hours ago
3 medium

uestions I have does anyone else have crying over nothing . or laughing at stuff Thu

Like watching something on tv or talking about something that's sad for other people and you just start to cry.

posted 6 days ago
A MyMSTeam Member said:

I'm sorry praying for you

posted about 7 hours ago
2 medium

Switch from Avonex to Aubagio

Has anyone have switched from Avonex to Aubagio? Just saw my Neuro today and we talked quite a bit about switching drugs. He understands my hesitation since I'm stable on Avonex. He mentioned needle fatigue but I really don't have that. He's not pushing me to switch so there's no pressure but I'd appreciate any feedback...pros or cons. Thanks. Deanna

posted over 1 year ago
A MyMSTeam Member said:

Deanna if it were me I would say why fix something that isn't broke?? Meaning your current med avonex is working, why stop and go to something else that… read more

posted over 1 year ago
5 medium

Inability to regulate body temperature?

Does anyone else experience this all day, every day? It isn’t hormones and this is completely separate from the heat-related exacerbations every summer when we now have heat waves here for weeks on end. Those flares are hellish and last for months with horribly disabling symptoms. This doesn’t necessarily increase or decrease any of my ongoing symptoms, but it IS frustrating and bizarre. It’s fairly new (within the last few months) and isn’t related at all to what I’m… read more

posted 7 days ago
A MyMSTeam Member said:

Terrible horrible night after night. It's a constant battle. Doesn't matter where I sleep; couch, under a glacier, Sleeping in the freezer, nothing… read more

posted 1 day ago
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