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

Scleroderma & Raynaud's UK (SRUK)

10,833 members5,407 posts

All posts for March 2020

Won my pip

hi everyone had a fone call today won my pip back after 12 month stress all back...
Sarog72 profile image

HERBAL REMEDIES FOR CALCINOSIS? CHANCA PIEDRA TEA OR ESSAIC TEA?

Hi everyone, Let me 1st start off by saying I absolutely love this group! I just...
DaisyLA profile image

Rheumatology 2nd appointment

I had my first rheumatology appointment earlier this month and had several blood...
Kels1974 profile image
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IS COLLAGEN SUPPLEMENT SAFE?

Hi all - Does anybody know anything about marine collagen/hyalauronic acid suppl...
DaisyLA profile image

Please help

I have limited systemic scleroderma/raynauds/calcinotis cutis and I’m a 36 year ...
DaisyLA profile image

Nitro cream use for Raynaud's?

Hi everyone, has anyone ever tried nitro cream for Raynaud's on hands? My Dr jus...
beaglab profile image

Conference call

Just a gentle reminder about the conference call tomorrow (Sunday)Any problems, ...

I feel electric flow throughout my body

I am a Buddist I started meditation about 2 years back. While doing meditation I...
helita profile image

New Raynaud’s Diagnosis

Hi All I was diagnosed last week with Raynaud’s having had numbness and pain in ...
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wales

Hi all,does anybody know if the warning letters apply to Wales. I have systemi...
haulotte profile image

No letter?

I was expecting to recieve a letter about being in the high risk category for co...

Who is on this Govt list then?

I cannot find out if I am on this so-called ‘vulnerable’ list however on the RA ...

Doubts about lupus

Hello all, My name´s Fiorella and I was diagnosed with primary Raynauds 5 years ...
Fiorella profile image

meeting replacement with weekly conference calls to alleviate worry's around covid 19 around the West Midlands area.

Hi folks, I have been asked if we can have weekly conference calls with all the ...
avtargill31 profile image

Limited cutaneous systemic sclerosis, secondary Raynauds and IEM versus COVID-19

Hello Reading confusing reports about this, should we who have this be self isol...
-missymoo profile image

High risk

Hi does anyone know if we with raynaurds are high risk?
Verily profile image

Birmingham meeting postponed

Hi folks, it’s with deepest regret that I’ve been asked to postpone our May meet...

Novel Coronavirus (COVID-19) advice for our community

Hello Everyone, We have published the latest information on Novel Coronavirus (...
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Any advice?

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

Raynauds and Scleroderma - Stinging, inflammed and sore finger tips!

Got 3 stinging fingers on my right hand.The middle one being the most troublesom...
eembee1 profile image

Need advice!

In February my right hand (specifically just fingers) suddenly swelled up two ti...

Coronavirus

Hi I have interstitial lung disease as per scleroderma. Naturally worried abou...
NSV69 profile image

Does this look like raynauds?

My hands, nose and feet are always cold.I have my first rheumatology appointment...
Kels1974 profile image

I get like an electric shock feeling that runs through my body, has anyone else experienced this?

Everytime I'm with my partner, we're making love, everything is going fine until...
John1212 profile image

Any one else having leg problems.

Hiya I have had always had a problem with cold hands and feet . Just over a year...
Amaya55 profile image