Posts - Hughes Syndrome APS Forum | HealthUnlocked

Hughes Syndrome APS Forum

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All posts for February 2015

What causes the cognitive issues in APS?

I've read sticky blood can be the cause, lowering oxygen delivery to the brain. ...
drob32 profile image

Sudden high pitched whine in right ear.

About a week ago I was lay on the sofa and very suddenly got really sick and diz...
Tomcat profile image

Need APS doctor in Sutton Coldfield near Birmingham.

My husband has been confirmed as having APS after a 3rd recent stroke. He was ev...
Vespa1 profile image
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Foggy head and jaw pain.

As an Hughes Syndrome patient I'm aware of foggy head symptoms which I'm curren...
JoJo0405 profile image

Muscular pain in arms/shoulders - lupus flare or low INR?

Does anyone else suffer with bad muscular (rather than joints) pain and heavines...
frankie100 profile image

Any APS doctors in Maryland/Delaware/Virginia

I was searching for doctors using google, but I wanted to see if anyone knew of ...
drob32 profile image

MTHFR C677T, MTHFR A1298C and Factor XIII related with lupus anticoagulant?

Hi to all! After my second miscarriage i have done some genetic tests. I have mu...
dea29 profile image

Vit.d

Hi! My vit.d is 14 ng/L and my endocrinologist said that i should drink 3 drops ...
dea29 profile image

A prof.or dr. Specializing in Hughes syndrome

Does anyone have a prof they see in France or any country in Europe easily acces...
designer16 profile image

APS antibodies, non typical symptoms

I just had the Cyrex Assay #5 done, which tests for most known autoimmune antibo...
drob32 profile image

costochondritis

have had a virus for the last 8 days,went to Drs yesterday, saw one who I have n...
donnabrain profile image

Can I do an assault course on warfarin?

As a fundraiser the charity I work for are doing a sponsored assault course.... ...
Lucky67 profile image

APS antibodies

What is the differance between having the APS antibodies and not having the synd...
sleepy3 profile image

TIAs or seizures?

Hi everyone, I was diagnosed with APS with chorea in January and, because of whi...
minnime63 profile image

Anti phospholipid antibodies and cerebellar ataxia

Hi all, whilst investigating my own particular health issues I came across the ...
lloydyuk profile image

Article: doctor on importance Vitamin D in APS patients

"Vitamine D deficiency [2] is common among APS patients and is associated with c...
Tranquility1 profile image

Tooth problems

Hi all Just want to ask if anyone else with APS suffers with tooth sensitivity ...
ledlegs profile image

Brain fog. Could transfats be a part of the problem

Just seen this http://articles.mercola.com/sites/articles/archive/2014/12/02/tr...

were in the daily mail again!!!

just a shame that they never go into more detail and just simplify it like its '...
emmaj profile image

Is scratching related to APS?

Hi! I feel scratching(my legs and lower back) for three months. Is it related wi...
dea29 profile image

A great article from The Daily Mail

http://www.dailymail.co.uk/health/article-2960372/Woman-heartbroken-SEVEN-miscar...
MaryF profile image
Administrator

interesting find

Hi all, new here as although I have had a diagnosis of APS for 8 years I didnt k...
barb64 profile image

IgG antibodies, translation please

I have been told my IgG anticardiolipin antibodies are elevated at 26, my beta2g...
Twadd profile image

Recommended food according to my condition(lupus anticoagulant and hypothyreosis)?

Hi to all! I will be grateful if somebody tell me advice about recommended food ...
dea29 profile image

After c section

I would like to announce that my baby girl was born healthy 3 weeks ago and she ...
Glassart profile image

Map Your GP

Hi all, It has become apparent through my enquiries that there is a need for a t...
NaggingWife profile image

Muscle Twitches and Hughes ?

Hi, In currently I am not diagnosed with APS, but my Beta-2 Glycoprotein 2 IGM i...
Jimalos profile image

Opinion about my problem

Hi! I`m new on this forum. I`m 29 years old and I`m from Macedonia. I`m glad tha...
dea29 profile image

Anyone know a GP in Salisbury who has APS experience?

We have recently moved to Salisbury, but simultaneously my husband was found to ...
NaggingWife profile image

Anyone IgA Deficient with APS? Sarcoidosis APS

My nearly 50 year old husband has just been diagnosed with APS after 2 different...
NaggingWife profile image