Hi can anyone give me some advice on Livedo Reticulairs please, I have been to GP but they don't seem interested, I had blood test weeks ago an when ask about it they just say nothing is wrong thanks .
Livedo Reticulairs : Hi can anyone give... - Scleroderma & Ray...
Livedo Reticulairs
![Seeley profile image](https://images.hu-production.be/avatars/d0aefb0c5899494b885d0896e68ffb02_small@2x_100x100.jpg)
Written by
![Seeley profile image](https://images.hu-production.be/avatars/d0aefb0c5899494b885d0896e68ffb02_small@2x_100x100.jpg)
Seeley
To view profiles and participate in discussions please or .
Read more about...
1 Reply
•
Hi Seeley,
Sorry to hear you're not getting the support you need from the GP etc.
I was recently diagnosed with livedo reticularis by my scleroderma specialist rheumatologist. He said it's not something that is significantly worrying, and is normally controlled quite well by low dose aspirin daily, which is what he has prescribed me with. The hope is that this will also help with my Raynaud's symptoms, as the aspirin should help to increase the amount of blood reaching my extremities.
Hope this helps and that you get support where needed soon.
Thanks,
Sara
Not what you're looking for?
You may also like...
Medication
Hi can anyone tell me what medication they are on for Raynauds as I have been told by the doctors...
Suspected Raynauds - guidance needed
First time poster here. I've been concerned for a while about my hands. I've been feeling the cold...
Silver ring splints
My rheumatologist is sending me off to see a 'hand therapist' in September. I think in may be an...
Royal Free visit
Hi all,
I just thought I would give a quick update.
I attended the Royal Free Hospital last...
Just diagnosed officially - Heated gloves on the NHS? What are they like?
I've had Raynaud's for aaaaaaaaaaaages but I finally saw a Rheumy who officially diagnosed me and...