Hughes Syndrome APS Forum | HealthUnlocked

Hughes Syndrome APS Forum

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Might be diagnosed with Antiphospholipid Syndrome (APS)

Hi I previously in January 2023 was diagnosed with PE, the past year has been d...
Summer133 profile image

Low O2

CAPS survivor here. Lately my O2 has been consistently between 87% -93% resting ...

Persistently low INR

For the past 12 weeks or so, I've had a persistenly low INR, ranging from 1.2 to...
henyrjonze profile image

extremely high inrs for aps

I've had my inr past 10.8 and had to receive plasma 2 days ago it was 9.9 they...
shinyeyes profile image

Parathyroid

I am booked in for a Parathyroidectomy and I just wondered whether my APS, as an...
Raschen profile image

Dentist asking for INR Test Results

Last week my dentist asked me for my INR test results. I'm a little suspicious ...
helendr profile image

Hotelfanatic

Hi everyone,I'm new to this group,was diagnosed with Aps 2020 after a miscarriag...
Hotelfanatic profile image

Phosphatidylserine

I thought I posted here about phosphatidylserine but can't find it now.... Does ...
Coppernob profile image

Nosebleeds

Hi, How many of you are getting regular nosebleeds that continue for an hour or...
Madmumma profile image

Warfarin & Tattoos

Hi everyone, since I started on warfarin I’ve not had any more tattoos, (NHS rec...
JollySailor profile image

Medsil

I had microblading 18 months ago.I stopped my riberaxaban for 2 days, I had no p...
Medsil profile image

anyone near LBI in NJ?

I am in Barnegat/Manahawkin now
Wittycjt profile image

microblading

I need advice on whether eyebrow microblading is safe if taking 10 mg Rivaroxiba...
Hockeysticks profile image
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About us

Hughes Syndrome - APS Support is a Forum that helps support people with Hughes/Antiphospholipid Syndrome and S...

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