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Experiences with
Chilblains
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Chilblains. Any Recommendations?
I’m not sure if my right hand has erupted with multiple
chilblains
or it’s something else. Does anyone have any recommendations for an interim home remedy for
chilblains
? The something else may be from trying to sort out what needs to be declutterred from my house prior to moving.
I’m not sure if my right hand has erupted with multiple
chilblains
or it’s something else. Does anyone have any recommendations for an interim home remedy for
chilblains
? The something else may be from trying to sort out what needs to be declutterred from my house prior to moving.
Lupiknits
in
Scleroderma & Raynaud's UK (SRUK)
4 months ago
Painful toes - mother with CBD
My mum has CBD, and whilst still able to walk, has decreased mobility and has been suffering from painful toes, initially from
chilblains
, but still complaining of discomfort months later. Is this a symptom of CBD?
My mum has CBD, and whilst still able to walk, has decreased mobility and has been suffering from painful toes, initially from
chilblains
, but still complaining of discomfort months later. Is this a symptom of CBD?
PeterPanandLostBoys
in
PSP Association
2 months ago
Cold water swimming
(Now I'm no longer on the brink of
chilblains
at all times it seems like it could be a reasonable endeavour!) Does anyone do cold water swimming (or similar) and feel any benefit?
(Now I'm no longer on the brink of
chilblains
at all times it seems like it could be a reasonable endeavour!) Does anyone do cold water swimming (or similar) and feel any benefit?
WitchingHour2point0
in
Thyroid UK
4 months ago
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Has anyone been prescribed Fluoxetine for Raynaud's?
I don't get full blown 3 phase Raynaud's attacks these days but my fingers are often blue for long periods of time despite being in a warm environment and my feet suffer quite badly, they are white and I get
chilblains
in winter sometimes with very nasty purple blisters which are extremely painful.
I don't get full blown 3 phase Raynaud's attacks these days but my fingers are often blue for long periods of time despite being in a warm environment and my feet suffer quite badly, they are white and I get
chilblains
in winter sometimes with very nasty purple blisters which are extremely painful.
lynntregaron
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
Hyponatremia, Raynaud's and P.S.V.T
Raynaud's which I have had since my 20's suddenly began to cause me problems: Pains and blotchy finger joints and
chilblains
. I am also feeling very depressed and lethargic. My bisoprolol has been increased to 2.5 mg daily and I have been started on nifedipine.
Raynaud's which I have had since my 20's suddenly began to cause me problems: Pains and blotchy finger joints and
chilblains
. I am also feeling very depressed and lethargic. My bisoprolol has been increased to 2.5 mg daily and I have been started on nifedipine.
Mstislav
in
British Heart Foundation
1 month ago
What on earth is Chilblains Lupus?
What I do know is it shouldn't be confused with lupus pernio but it is, confusingly, also called pernio or perniosis.After a lot of googling I think that my worsening/changing Raynaud's sounds like
Chilblains
Lupus.
What I do know is it shouldn't be confused with lupus pernio but it is, confusingly, also called pernio or perniosis.After a lot of googling I think that my worsening/changing Raynaud's sounds like
Chilblains
Lupus.
Brychni
in
LUPUS UK
3 months ago
Anyone else driven crazy by Chilblains
The
chilblains
along with some of the other bits (repeated mouth ulcers, and the old neck pain) make me wonder if this could be something else coming to join the party...
The
chilblains
along with some of the other bits (repeated mouth ulcers, and the old neck pain) make me wonder if this could be something else coming to join the party...
softekcom
in
PMRGCAuk
6 months ago
Iloprost infusions
Chilblains
at this time of the year add to the pain. I have tried Sildenafil (but couldn't tolerate the side effects) and for a while now have been on Amitriptyline (or Nortiptyline), and Pregabalin. So far, nothing has relieved the pain in my feet.
Chilblains
at this time of the year add to the pain. I have tried Sildenafil (but couldn't tolerate the side effects) and for a while now have been on Amitriptyline (or Nortiptyline), and Pregabalin. So far, nothing has relieved the pain in my feet.
skylark15
in
LUPUS UK
5 months ago
Iloprost infusions
Chilblains
at this time of the year add to the pain. I have tried Sildenafil (but couldn't tolerate the side effects) and for a while now have been on Amitriptyline (or Nortiptyline), and Pregabalin. So far, nothing has relieved the pain in my feet.
Chilblains
at this time of the year add to the pain. I have tried Sildenafil (but couldn't tolerate the side effects) and for a while now have been on Amitriptyline (or Nortiptyline), and Pregabalin. So far, nothing has relieved the pain in my feet.
skylark15
in
Scleroderma & Raynaud's UK (SRUK)
5 months ago
Good vibes please...
- repeated
chilblains
. - 'chicken skin' on the inside of my knees - strange pain in my left heel/sole when i walk - Skin on my fingertips thickening and splitting, making housework very difficult. I thought it was dryness. But the usual moisturisers aren't working.
- repeated
chilblains
. - 'chicken skin' on the inside of my knees - strange pain in my left heel/sole when i walk - Skin on my fingertips thickening and splitting, making housework very difficult. I thought it was dryness. But the usual moisturisers aren't working.
softekcom
in
PMRGCAuk
5 months ago
Fibromyalgia action group
In winter this leads to
chilblains
sometimes. In summer to keep them cool I place a hot water bottle from my freezer (nice and cold) and place my feet on that. I have an added Dome mattress topper to make my bed more comfortable.
In winter this leads to
chilblains
sometimes. In summer to keep them cool I place a hot water bottle from my freezer (nice and cold) and place my feet on that. I have an added Dome mattress topper to make my bed more comfortable.
PlantFoods
in
Fibromyalgia Action UK
2 months ago
Fingertips, toes
I used to get what I think must have been
chilblains
on my toes in really cold weather but they were never painful or itchy. Also never had them on fingers until now.
I used to get what I think must have been
chilblains
on my toes in really cold weather but they were never painful or itchy. Also never had them on fingers until now.
Brychni
in
Scleroderma & Raynaud's UK (SRUK)
4 months ago
Figuring things out - first year since diagnosis
I was diagnosed just over a year ago following about a year of strange symptoms - GI issues, weight loss, Raynaud's, mouth ulcers, hand and wrist pain and swelling, unexplained fevers,
chilblains
, hair loss and funny rashes.
I was diagnosed just over a year ago following about a year of strange symptoms - GI issues, weight loss, Raynaud's, mouth ulcers, hand and wrist pain and swelling, unexplained fevers,
chilblains
, hair loss and funny rashes.
CGSLE
in
LUPUS UK
3 months ago
Notes for upcoming GP appointment
Background – my symptoms and current diagnoses
You will be able to see from my medical notes that I was diagnosed with Reynaud’s Syndrome and Chronic Blepharitis in my early teens, resulting in regular
chilblains
, swelling and discomfort to both hands and feet: and repeated styes/chalazions in
Background – my symptoms and current diagnoses
You will be able to see from my medical notes that I was diagnosed with Reynaud’s Syndrome and Chronic Blepharitis in my early teens, resulting in regular
chilblains
, swelling and discomfort to both hands and feet: and repeated styes/chalazions in
Wispymisty
in
LUPUS UK
2 months ago
Symptoms of cutaneous lupus
Subacute cutaneous Lupus..hair loss and lupus
chilblains
!!
Subacute cutaneous Lupus..hair loss and lupus
chilblains
!!
Joanus
in
LUPUS UK
1 year ago
Apixaban - and my toes
Checking up on images, the nearest I could find were
chilblains
. An issue I have absolutely never previously had. (I'm not 100% sure - no pain, just an odd sensitivity and a bit swollen, and shiny!) So I quit the Apixaban - and my toes have returned to my normal over about three weeks.
Checking up on images, the nearest I could find were
chilblains
. An issue I have absolutely never previously had. (I'm not 100% sure - no pain, just an odd sensitivity and a bit swollen, and shiny!) So I quit the Apixaban - and my toes have returned to my normal over about three weeks.
Carew
in
Atrial Fibrillation Support
1 year ago
chilblain damage to finger nails?
I have UCTD and reynauds but this is the first time for finger
chilblains
. Any thoughts are welcome!
I have UCTD and reynauds but this is the first time for finger
chilblains
. Any thoughts are welcome!
redmaggie
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
chilblains
Does anyone else have problems with
chilblains
? I take apixaban and for the last few years winters have been a misery with
chilblains
on my right ear, my toes but mostly my fingers-they stay swollen and stiff till the weather warms up.
Does anyone else have problems with
chilblains
? I take apixaban and for the last few years winters have been a misery with
chilblains
on my right ear, my toes but mostly my fingers-they stay swollen and stiff till the weather warms up.
123Abc123
in
AF Association
1 year ago
chilblains
I get Raynaurds and together with lupus my hands get really raw and saw like
chilblains
. I was advised to use cetreben handcream and take a piriton. Anyone else tried piriton?
I get Raynaurds and together with lupus my hands get really raw and saw like
chilblains
. I was advised to use cetreben handcream and take a piriton. Anyone else tried piriton?
0105luppyabby
in
LUPUS UK
1 year ago
Chilblains
Anyone with
chilblains
on their toes? How do you manage with shoes?
Anyone with
chilblains
on their toes? How do you manage with shoes?
Jacko37
in
Scleroderma & Raynaud's UK (SRUK)
2 years ago
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