Posts - Hughes Syndrome APS Forum | HealthUnlocked

Hughes Syndrome APS Forum

10,397 members10,602 posts

All posts for June 2012

Anyone got any bright ideas on how to deal with oral allergy syndrome - particularly problems eating fruit?

I have Hughes, Sjorgrens, Fybromyalgia plus a few other things thrown in. I hav...
DorothyItaly profile image

Can anyone help with experience of Dental Implants with Hughes or other autoimmune diseases?

I am worried about the effect on Hughes syndrome, or impact on autoimmune disor...
CarolBSL profile image

holiday insurance

Hello well we are going to holiday in UK as thought we would do a last minute ho...
daisy11 profile image
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Hello, I was wondering how many Hughes sufferers (APS) also have problems with periodontitis?

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symptoms worse since having a baby, is this normal?

Hey! I was just wondering if any ladies had experience worse symtoms after havi...
kay19987 profile image

Current Radio 4 programme live for a short while: and relevant newspaper article:

1. http://www.guardian.co.uk/healthcare-network/2012/jun/11/patient-from-hell-...
MaryF profile image
Administrator

For all you located in the USA - a useful resource - in case it is of interest!

Hi there. Most of you will have at some point come across this very profe...
MaryF profile image
Administrator

Waiting on my results but what a palava trying to get tested.

I read the article in the Sunday Mail a few weeks ago and alarm bells started ri...
Leelaked77 profile image

A break in the pain

Hi there, I just have to share this to you... Maybe this is old news for you, bu...
BrazilianBade profile image

I think we need to rethink our strategy on our posts on this forum regarding consultations ...

I am going to start off by saying please do not get the wrong impression about w...
travelnut profile image

Anyone know of a specialist pregnancy unit that deals with Hughes?

hi, after 3 miscarriages I have been diagnosed with Hughes and Factor v Leiden, ...
Kimmichelle86 profile image

Uncle Benny!! :-) :-) :-)

Hi Jet Home and up and about, take it easy, no doing too much, the witches are ...
jessielou profile image

Do confirmatory tests have to be positive for Hughes Syndrome?

I tested positive for lupus anticoagulant in the hexagonal phase after developin...
camerel profile image

WOW -cost of insurance

I cannot believe it - I have just been quoted over £500 for travel insurance for...
Lesley_D profile image

Please Please Help, do not understand what my GP has told me and unsure as whether I have Hughes or not.

I think (think being the operative word) that I have recently been diagnosed wit...
dragtalav profile image

need help pls

I've had a neurological condition for 8 years or maybe longer and was diagnoised...
nay87 profile image

Thank you

I still find it hard to understand how some doctor's and professionals can treat...
Beckyl1 profile image

I swear I'm going mad!

I'm 20 and know I have APS. All the symptoms are there. I had a DVT when I was 1...
MJLS profile image

Can someone help with talking me through costing for St Thomas

I'm looking at referring myself or going private. Can anyone give me some advice...
MJLS profile image

How do we get doctors to believe that moving blood clots can be felt?

It's infuriating! We are fed up with doctors telling us "You can't feel a blood ...
sbncmo profile image

Joint/ Muscle pain that 'moves' around body

Hi everyone! Does anyone have joint and/or muscle pain that seems to migrate ...
Hilariew930 profile image

Update

Bliemy well to update i am now taking 3 doses of 1200mg of gabapentin a day, on ...
Beckyl1 profile image

Brain fog

When does 'brain fog' stop being brain fog and start becoming something you nee...
margaretjo profile image

An added post to Sheena's post to our Jet!

Just a pic' for you bud for when you can view it....thought it might cheer you u...
Suzypawz profile image

Here we go.... big drum roll etc

As we approach the 800 mark with members, welcome everybody, this is growing fas...
MaryF profile image
Administrator

Atypical symptoms to APS??

I wondered if anybody else encounters the frustrating problem of when you see yo...
traceylou profile image

I'm Back

Hi all (I'm typing this with a smile) How are you all. I just wanted to say...
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Does APS have a symbol? Some kind of sign?

Hey guys, as per the question mentioned, do we have a sign like a ribbon in AIDS...
BrazilianBade profile image

Positive thoughts and good wishes, lots of luck to Jet!!!!! :-) :-)

Hi all I'm sure I speak for everyone in sending all the best, lots of luck and ...
jessielou profile image

APS in kids

Hi there, Have you got any news about APS in kids?. I've just heard about a 4...
David_Madrid profile image