Posts - Hughes Syndrome APS Forum | HealthUnlocked

Hughes Syndrome APS Forum

10,354 members10,542 posts

All posts for November 2023

microbleeds

Hi I wondered if any of you have had micro bleeds in the brain and had to theref...
chelb29 profile image

What doesn't mix well with Coumadin?

Hello, my name is Chris from french part of Canada, please forgive my poor Engli...

The Mind Body Connection with APS and any autoimmune disease

Hi again, I’m an Osteopath, Naturopath, Medical Acupuncturist etc and it took 20...
Madmumma profile image
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APS/POTS

another issue I would like to raise. Do the people with POTS also suffer from ch...

APS/Pots

could you guys share is anyone else has APS and POTS combined ? Was POTS diagnos...

This might help someone ?

Hi Everyone Just wanted to post some information that might be useful. I have f...
Tennisbum profile image

Coming home

So after 4.5 years in Nigeria and an APS diagnosis in summer 2020 I’m coming ba...
GillyA profile image

night sweats

I got aps sticky blood I been to seen once in the last 8 years think they forgo...
johncarver profile image

Having a seriously bad year

As per the title, I’m having one hell of a year.. Last year I had awful pains i...
Tomcat profile image

APS Symptoms

As many of you know I have been diagnosed with Sjogrens Syndrome, Lupus, Fibromy...
WendyWoo50 profile image

warafin and hairloss

hello- my daughter (12 years old) was recently diagnosed with APS - double confi...

I’m still not convinced

Hi Don’t want to name and shame any medical professional on here but will tell...

Change in range

Hi everyone hope you are all good I saw pharmacist today at St Thomas’ instead ...
APSGirl22 profile image

Feliz em participar , fui diagnosticada com síndrome do intestino irritável ,e estou aqui pra ficar atualizada e saber mais sobre o assunto

Passei por muitos médicos e com dores e todos os sintomas que a sii nos fornece...
Siiexplorer profile image