RLS with much more: I am exploring beyond... - My MSAA Community

My MSAA Community

9,248 members21,016 posts

RLS with much more

Wanted-sleep profile image
4 Replies

I am exploring beyond just my having RLS.

Any sharing from others that have/had RLS that was later labelled MS would be very welcome.

I know and feel there is so much more going on than just RLS.

Ailments/symptoms that pop up like a light swith just to be turned off after a lapses in time is concerning and annoying. There are several.

Each hand and wrist

Sole of right foot in pain off/on for weeks.

Tennis elbow even though never held a racket in years yet it has been a couple of months waiting for it to return to normal.

Weeks of a plugged ear misteriously disappears and returns to normal.

Neck and back pains just come and go?

Feedback most welcome. Advise for fixes.

MS or not?

Written by
Wanted-sleep profile image
Wanted-sleep
To view profiles and participate in discussions please or .
4 Replies
NorasMom profile image
NorasMom

I've never been diagnosed with Restless Legs, but one of my first MS symptoms was leg issues. I had the twitchiness and weird aches regularly at night. Sometimes, they'd be so bad that I'd cry myself to sleep. Are you feeling a heaviness in one or both legs when you walk any distance in hot weather? Or you reach a point where your legs just won't move for a bit and then suddenly they're fine after you pause for a minute or two?

PWilli profile image
PWilli

I had Passive Leg Movement Disorder before being diagnosed with MS. Now I have both. I don’t have the RLS sensations, my legs are in motion while I sleep - I was unaware of it until a sleep study. Some nights when I crawl in bed I accuse my husband of moving his legs and then find out it’s actually mine moving. 😜

Frances_B profile image
Frances_B

Re your question "MS or not?". No-one here can tell you - you will need to talk to your doctor and if they think it necessary you can be referred to a neurologist for appropriate tests. There are many MS mimics which only doctors can rule out through doing relevant tests - it's not as simple as matching a list of your symptoms with those you can find online from people in chat rooms like this one and then asking those people if they think you have MS. The causes of what is causing your symptoms could be several unrelated problems.

Tazmanian profile image
Tazmanian

Make sure you see an ms neurologist

Not what you're looking for?

You may also like...

As the Clash says, should I stay or should I go?

Today was that ever elusive good day, when I’m sure I can drive and be ok long enough for there and...

Stormy 2nd Surgery

My poor pup has to have surgery again tomorrow morning to remove his dew claw. It just hasn’t...

Daughter has Cancer

I told you that my dog had surgery Friday morning, but my day went downhill from there fast. Emily,...

Can Anyone Who has Discontinued Ocrevus Please Tell Me What Happens With Crap Gap Symptoms?

Hi all, I posted a while back about stopping Ocrevus and starting Mavenclad. I am turning into a...

Heat and MS

I would like to know how Heat affects the MSers on this site. It can make me slow and sluggish but...