I'm new here with Schamberg's Purpura - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,402 members10,612 posts

I'm new here with Schamberg's Purpura

Mothersh1p profile image
4 Replies

I have been told I have Schamberg's Purpura. I'm 63. It is mainly on my lower legs and comes and goes but never goes away completely. It started on the tops of my feet but cleared up completely after a few years only to return on my lower legs. The bright red dots do fade eventually, like bruises but are replaced by more almost immediately in other places. I'm not overweight, very healthy and keep very active. Nothing seems to affect the rate of occurrence of the dots or clear them up. My doctor says there is no treatment and that I just have leaky veins as I have thread veins. Has anyone any advice or self help for keeping the dots to a minimum? Are there any effective treatments at all?

Written by
Mothersh1p profile image
Mothersh1p
To view profiles and participate in discussions please or .
Read more about...
4 Replies
MaryF profile image
MaryFAdministrator

Hi there, have you also got a diagnosis of Hughes Syndrome/APS? This forum is specifically for Hughes Syndrome/APS. Do you need me to help you find a forum? MaryF

Mothersh1p profile image
Mothersh1p in reply toMaryF

Thank you! I only noticed I was on the wrong forum as I posted the message. How do I find the right forum please?

MaryF profile image
MaryFAdministrator in reply toMothersh1p

If you look at the top under communities, it will let you scroll through the list of every group/charity on here. Failing that, this here, has a list on the left hand side of all possible support groups: pcds.org.uk/p/the-primary-c...

To leave us, and travel onwards, just unfollow us, best of luck. MaryF

ps there is a Facebook group: facebook.com/Schambergs/pho...

Mothersh1p profile image
Mothersh1p

Thank you!

Not what you're looking for?

You may also like...

I'm new to this :/

Hello everyone, this is all new to me but I need someone who understands. I feel so alone. I am...
Charli84 profile image

Up to date with APS/THYROID/LUMPS on the hand etc

I last wrote on here because of the conflicting opinions about all my health problems. I'm on...
Teanna profile image

Any APS'ers have issues with petechiae

I've recently noticed petechiae on my lower legs and feet. Have any of you guys here experience...
mylafont profile image

New here...anyone from Ontario?

Hi there, I have APS and moved to Ontario (near London) from Alberta 3 years ago. I have yet to...

Hello, I'm new here.

Hi, everyone. I'm new to the forum and want to say hi. I had my pulmonary emboli in Aug. 2018 and...
niloreid2 profile image

Moderation team

See all
KellyInTexas profile image
KellyInTexasAdministrator
HollyHeski profile image
HollyHeskiAdministrator
lupus-support1 profile image
lupus-support1Administrator

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.