Hi,I’ve noticed my right foot is red lately.I also have drop foot.Is circulation problems and m.s. go together?Does anybody experience this?Thank you
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We were excited to get going!
And hit a few bumps along the way…
However, in all seriousness, we remain grateful for our amazing volunteers, members & all who have made MSWorld a valuable resource for all!
July 10, 2024, we celebrated the goodness of these past 28 years. With a heavy heart, we will be ending our services.
We need a financial miracle to keep going forward.
We thank all for your support.
MSWorld's website will close on October 16, 2024.
“I personally want to wish all of you the guidance to find this type of support, as so many do here. Also, my prayers and love extends beyond my understanding. It has been a pleasure to steward this journey.”
God Bless you, Kathleen
Kathleen Wilson
Founding President
❤️
we leave knowing that
we did our best and
stayed true to our mission and purpose.
Please visit our General Questions and Answers forum to read more.
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Circulation and m.s.
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I don't personally have that problem, but I've read that it can be an issue.
Here's an article that describes some symptoms and offers some tips.
https://www.msfocusmagazine.org/Maga...ation-Boosters~ Faith
MSWorld Volunteer -- Moderator since JUN2012
(now a Mimibug)
Symptoms began in JAN02
- Dx with RRMS in OCT03, following 21 months of limbo, ruling out lots of other dx, and some "probable stroke" and "probable CNS" dx for awhile.
- In 2008, I was back in limbo briefly, then re-dx w/ MS: JUL08.
- Betaseron NOV03-AUG08; Copaxone20 SEPT08-APR15; Copaxone40 APR15-present
- Began receiving SSDI / LTD NOV08. Not employed. I volunteer in my church and community.
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Yes I have this only it’s my left foot. I’m afraid it’s all MS related and there’s not a darned thing we can do about it. Sorry to be the bearer of bad news and not sounding very optimistic. It’s got to do with the nerves that automatically increase or decrease blood flow to the extremities. I find it all too hard to understand completely and maybe someone else can shed more light on it. Just letting you know it’s not just you.It was one agains't 2.5million toughest one we ever fought.
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Originally posted by Carlyle View PostHi,I’ve noticed my right foot is red lately.I also have drop foot.Is circulation problems and m.s. go together?Does anybody experience this?Thank you
My entire right side is affected by MS and I have foot drop too, along with a red (sometimes purplish when cold) right foot. My right hand becomes discolored also.
Originally posted by oceanpride View PostIt’s got to do with the nerves that automatically increase or decrease blood flow to the extremities.
Elevating my legs in the recliner several times during the day is helpful.
Take CarePPMS for 26 years (dx 1998)
~ Worrying will not take away tomorrow's troubles ~ But it will take away today's peace. ~
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It's good to know I'm not the only one with this problem. My pcp was alarmed and had me take a test for PAD (peripheral arterial disease) using an ultrasound. Everything checked out OK.
I elevate my right leg and foot during the day too. I also have Raynauds causing poor circulation. Exercise is good, but for me it's pretty limited.1st sx '89 Dx '99 w/RRMS - SP since 2010
Administrator Message Boards/Moderator
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Hi Carlyle,
I read the initial post and identified with your observation but hoped others would comment.
Simply was not sure that my MS was related to exactly what you described.
I noticed this red foot / cold foot problem once. On my MS affected side also. It lasted for maybe a month or so. That was over a year ago. Once and done? It returned to normal and has been so ever since although at times both feet are cold. Most likely a circulation problem.
One comment... Many who responded are PPMS, like me. Doubt this means anything.
Jer
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Hi Carlyle.
Before assuming it’s due to a circulation problem and\or MS please see your PCP to rule in\out any other health issue.
I have experienced swollen, red, and very painful feet. Both feet at the same time.
This happened twice as part of exacerbations, no steroids were used.
My feet stayed that way until the exacerbation resolved. Then my feet went back to normal and it never happened again.Diagnosed 1984
“Lightworkers aren’t here to avoid the darkness…they are here to transform the darkness through the illuminating power of love.” Muses from a mystic
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Red,swollen and ice cold feet
I just brought this up to my nuro. Yes it is MS’s fault.
same as Ocean it’s worse on my left side. My right leg spasms most, mostly in bed. End up alone a lot by morning. We make a joke of it, otherwise, well who knows.
Loved how someone said “dropped anchor” that’s exactly how it feels sometimes.
I personally have hot flashes run around the house 1/2 dressed with my feet bundled in fuzzy socks and slippers because they are freezing.
Nuro suggestion is a foot boot to keep my right foot up instead.hmmmmm we’ll see.
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