Posts - Hughes Syndrome APS Forum | HealthUnlocked

Hughes Syndrome APS Forum

10,356 members10,544 posts

All posts for November 2015

Some good news

My GP has confirmed that I was normal on the cardiolipin test so that is a huge ...
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Fab news for type 1 diabetics today

The telegraph have featured An article explaining that by injecting back in immu...
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Xarelto

Today i started on blood thinner and I'm on xarelto. Anyone who knows about it? ...
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Dr. Situnayake

Has anyone seen Dr S? Just wondered what your experience was?
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Looking for a great hematologist in Houston, Texas

If someone knows of a great hematologist in houston texas it would be greatly ap...

Manchester Specialist - Dr Thachil (haematology) at Manchester Royal Infirmary

I just wanted to share what I can only describe as an amazingly positive experie...

nerve conduction study says no peripheral neuropathy?!

Hello nice people! I'm in the UK.... I have quite a complex health history which...
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Hughes Syndrome Study

My name is Harriet and I am an undergraduate psychology student at Birkbeck, Uni...
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Any Information

Hey I finally found out which lupus I have and it's lupus anticoagulant also kno...
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My story

Hello I am 41 and a few weeks ago had a funny turn at work which I think was a r...
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HAPPY BIRTHDAY Professor Graham Hughes

Happy Birthday to Professor Hughes today! Wishing him all the best from our for...
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Stiff eye

Hello - from time to time over the last few weeks I have had an odd sensation in...
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Getting used to APS

Went into St Thomas' hospital in July because I was very breathless. They discov...
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Got my Thyroid Results

My TSH is 0.84 (standard range listed as 0.35-4.0) My Free T4 is 1.0 (standard r...
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Seronegative APS

Hi, just been to see my Rhumatologist this morning and I was pretty nervous. I b...

Newly Diagnosed

Hi I'm Debbie from Long Island, New York, USA! I'm a very happy-go-lucky person ...
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Seeing my Neurologist

Hi guys, Next Sunday (26th Nov) I'm seeing my neurologist for my results of m...
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HELP !!!! Although I've got APS, but I've got an another PE???

I've had APS for many years. I've also have a stent in my groin for which I had ...

Is this hereditary

Hi I'm Nanny23 my sister was recently diagnosed withAPS! Shud I also be tested!
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A round up of articles from the press

1. http://www.dailymail.co.uk/health/article-3326062/Could-WALNUTS-prevent-hea...
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Can I take iron supplements?

I have APS. I am on Warfarin and statins. Can I take iron supplements?
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Getting tested for thyroid

Hi Everyone, I know there have been many posts on here related to thyroid issue...
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Plaquenil

Hi there, has anyone had any trouble recently getting plaquenil from pharmacies ...
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APS with no painkillers

I am on this site and read about all the pain everybody have. I have only a litt...
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Only four days left to give feedback on the NHS

This was kept rather quiet, if you are in the UK do consider filling it in....
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Administrator

Neurologist Vs. Hematologist

Any help I can get with this would be great! I have heard a lot on here about fi...
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Hi Kerstin!

Hi Kerstin! So sorry I didn't know I was in Clair's site so sorry! Now I know! I...
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Headaches and aps

Hi! Does anyone else get headaches that start in the day and get really bad at n...
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A new paper on Hughes Syndrome/APS and the Kidney

Via HSF Facebook page: An helpful article has been written by APS experts loo...
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not getting any better

Hi all I am newly diagnosed and am in sunny Queensland Australia. I had several...
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