Any hints or tips?: Hi I was diagnosed... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

11,113 members5,638 posts

Any hints or tips?

SBrown1966 profile image
3 Replies

Hi I was diagnosed with Raynauds many years ago. Managed to ignore the symptoms when working. Now I’m not working I notice them more. I get achy legs a lot. I was wondering if anyone had any top tips to help with this. Thanks

Written by
SBrown1966 profile image
SBrown1966
To view profiles and participate in discussions please or .
3 Replies
Tiggywoos profile image
Tiggywoos

Hi SBrown . Sorry to hear about your legs but I can totally sympathise . Mine wake me up every night and are only relieved by getting up . It’s like someone is squeezing the calves . I’ve tried loads of things nothing sadly has worked for me . The only thing they helps a little is a heated blanket I got from Argos . Take care

Sophiebun11 profile image
Sophiebun11

Hi SBrown1966, It is no fun having leg spasms or cramps. They leave your legs so tired and painful afterwards.

When I'm flying out of bed in the middle of the night due to the cold and cramping I found a bizarre trick which helps me. I turn on my blow dryer and aim it at the area with the cramp. The heat increases circulation and relieves the spasm within 30 - 60 seconds. Before I figured out the blow dryer trick a spasm could last 10 - 20 minutes and make it so I couldn't stand or walk on that leg or it would get worse.

I wear a pair of leg warmers to bed which helps as well. With the feet cut out it doesn't make you too hot in the summer or fall. Then I add several thick socks too in the winter.

I just bought some compression stockings on Amazon. They are helping too. They have such cute ones now, I got dogs, cats, and assorted patterns in a 6 pack, not the ugly orthopedic ones. They might help you during the day with your achy legs. They even come thigh high if your aches go all the way up. In the winter nights my spasms go all the way up my inner thighs, those are the most excruciating ones.

Good luck, I hope you find a little relief.

🐇

Tiggywoos profile image
Tiggywoos in reply toSophiebun11

Great idea about the leg warmers 😊

Not what you're looking for?

You may also like...

Hints and tips please from my "Scleroderma family"? (new on this website)

Dear "family", It's been only a few days that I came across this forum and I've already found some...
tanya1981 profile image

Any advice?

Hey everybody! I got diagnosed Raynaud’s disease a while back now... I’ve dealt with multiple...

Hey i need some advice and any tips!!!

As it has started to get colder , im finding it hard to get anything out of the fridge or freezer.....

ulcerated finger tips

I have ulcerated finger tips, with horrible crusts. Does anybody have any suggestions on how to...
aramaya profile image

Just diagnosed scleroderma/myositis - any help or guidance appreciated

Hello all, First time posting…. I have noticed just how incredibly helpful and supportive this...
ruablue profile image

Moderation team

AnnabelSRUK profile image
AnnabelSRUKAdministrator
Chicunique27 profile image
Chicunique27Administrator
SRUKadmin profile image
SRUKadminPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.