Posts - Scleroderma & Raynaud's UK (SRUK) | HealthUnlocked

Scleroderma & Raynaud's UK (SRUK)

10,797 members5,387 posts

All posts for February 2013

Good news!

Just got a call from the GP I saw this morning who said she called the Royal Fre...
tcogb profile image

And the waiting continues..

Saw my favourite GP today. You know why she is my favourite? She actually turns ...
tcogb profile image

Very sore finger ...painful to the touch & swollen :(

My ring finger is so swollen & tender to the touch nasty sore red patch on one ...
AliW profile image
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Immunoglobulin G treatment

Hi everyone has anyone had this treatment ? if so what for ? and what did it en...

Coding and Health Unlocked

Hi folks... this is going to be a bit a none Raynaud's blog this time around. I ...
Blue-Bunny profile image

toxcillizumab

i have raynauds and diffuse systemic scleroderma i have tried chemo for 9 months...
llindylou profile image

Cure with Cayenne

Those of you suffering with hot feet or cold feet. Here is a major way to help y...
Yogananda profile image

Back to GP...again....

Still waiting for my appointment to come through since my referral to the Royal ...
tcogb profile image

Even with three pairs of gloves, the Raynaud's still gets me! been to the doctor but she says there's nothing she can do, is this true???

nicolanymph profile image

preparing fruit

well interesting day today, after having a fresh pineapple ripping on the window...
sandycharlie profile image

I get Raynauds in my hands . I've tried Losartan but it made no difference and am wondering if nifedipine would help.

I read Sandycharlie's post and it seems a lot of people take it with success. Wh...
DeedeeP profile image

Dilemma: Heating or Internet?

From my previous blog, you have have ascertained that my landlord hasn't put me ...
Blue-Bunny profile image

Just found this and thought i would share ;)xx

Dental/Raynaud's Disease Connection In my clinical experience since 1969, I ...

Keeping warm at football matches

Sorry those who do not like football! I am a keen supporter or my local team and...
Cammeronuk2 profile image

Continuous iloprost.....how long does it take to work?

I had continuous iloprost this week in hospital, went in on Monday and got out t...
scotgirl profile image

Anyone noticed that the RSA site is going reaalllly slowly?

I mean I have -_-; I'm still here waiting for it to load. I think people have be...
Blue-Bunny profile image

has any1 ever put a claim in against an employer? i have been told my raynauds poss caused by my last job as machine vibrated thro my hands

sandycharlie profile image

The Raynaud's Winter Survival Kit

Today I have spend literally the whole day putting together a list of (cost effe...
medsoph profile image

tissue damage following chill blains

i have suffered chill blain s as a result of secondary raynards for several wint...
moss profile image

Has anyone used any voice activated software in relation to Raynauds or any other medical conditions and what has their experience been?

In particular has anyone used Dragon software?
strained1 profile image

Hello kind people with Raynauds, Does anyone get the tingles all day long?

I was doing good but htan every other month or so my bicepts and thighs start ti...
danacetz profile image

does anyone find doing more exercise help with raynauds? (mine in hands only at mo), thinking bout getting exercise bike

sandycharlie profile image

exercise

been to the doctors and been referred to a rheumatologist so hopefully will get ...
sandycharlie profile image

Mouth ulcers and raynauds connection?

Hello, I've had raynuads for about 5 or 6 years now diagnosed and am 18, I've...
DeGreenifyMe profile image

Having problems with travel insurance as I have lung involvement with scleroderma

Hi, am new to this site. Have been dianosed with raynauds and systemic sclerosis...
Bubbles01 profile image

Skin rashes & large blister appearing overnight

After recent blood tests and years of various symptoms my GP has finally referre...
tcogb profile image

Pre-ulcer starting on my left outside ankle

I can't sleep because of the super strong needle sharp stabbing pains. Any sugge...
danacetz profile image

Full or Fingerless Gloves?

More of a poll really for those who have tried the RSA Silver gloves. I have a p...
Blue-Bunny profile image

Warming cream?

Not officially diagnosed (although I do have lyme disease). My hands are always ...
miffy profile image

So Many Questions.....

Well 3 months after doctors "diagnosis"most people talk about 1 or 2 fingers,all...
Montiedon profile image