chilblanes: I have developed chilblanes... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

11,113 members5,639 posts

chilblanes

fingers profile image
4 Replies

I have developed chilblanes on one toe and possibly on another any ideas on treatment's or remedy

Written by
fingers profile image
fingers
To view profiles and participate in discussions please or .
4 Replies
Smudge_Crawford profile image
Smudge_Crawford

Fingers, treatment for chilblains

Smudge_Crawford profile image
Smudge_Crawford in reply toSmudge_Crawford

Treatment for chilblains, I also have Reynauld's Phenomenon, and very low blood pressure, unfortunately to take the treatment to open up the blood vessels and prevent chilblains from forming, ypu need normal blood pressure 😢, my Dr tells me I can't take this because it would 'in his words' put me on on the floor, so he told me use 5% Ibroprophen gel on my chilblains and invest in some USB heated socks, which are wonderful, cost about £35, but well worth the money, if you have normal blood pressure I would suggest speaking to your Dr for advice

fingers profile image
fingers in reply toSmudge_Crawford

Thanks i have the opposite, high blood pressure, my doctor suggested calamine lotion ?

Glow-worm profile image
Glow-worm

Definitely wear warm wool socks - I mean thick walking-boot socks, especially in bed. (For my feet, the chilblains always seem to come on overnight.)

If need be, wear the next size up in shoes, so that you can wear thick warm socks and have less pressure on swollen toes.

Mine started in childhood, but I find now, with milder winters, I get chilblains less than I used to.

If you're new to chilblains, the big problem is damp. I can't tolerate damp cold (but quite like dry cold), and the same goes for my hands.

I have done lots of work outdoors over the years, and am perfectly capable of developing chilblains in June, if my hands are getting cold and wet for any length of time (welcome to the British Isles!).

I can't remember if I've tried calamine lotion for chilblains specifically, but I have used it for other skin itches. Post-Covid, it was hard to obtain for a while, but when I finally managed to obtain some it was in the form of Aqueous Calamine Cream (a mixture of calamine lotion with aqueous cream).

Not what you're looking for?

You may also like...

Methotrexate

I'm starting on 10mg on Sunday night (as I have a dressage competition on Sunday afternoon I'm...
Nikki246 profile image

Mycophenolate

Hi there I have limited scleroderma and I have been asked if I want to go on a trial study for...
SwanSRUK profile image

mycophenolate

Hey all, Any one on mycophenolate? Just wondering how everyone getting on with mycophenolate - i...
naila_007 profile image

Digital ulcers

Hope you are all keeping warm and safe. Does anyone have any tips on coping with ulcers on their...
Jacko37 profile image

Lesions in nose?

Hi! I have Limited Cutaneous Systemic Sclerosis--about 5 years now. Just curious--does anyone...
pallinurse 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.