Here we go: Only 8 more members signing... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,411 members10,622 posts

Here we go

MaryF profile image
MaryFAdministrator
7 Replies

Only 8 more members signing up and we will be '600'... not bad for such a short space of time!

M x

Written by
MaryF profile image
MaryF
Administrator
To view profiles and participate in discussions please or .
7 Replies
taffydaffy profile image
taffydaffy

Wow another 100 that was quick well done to you all your doing a great job x

7 more to go now! Will be reporting to the trustees this evening about the strength and numbers of our HU community :)

MaryF profile image
MaryFAdministrator in reply to

good good and goody x

paddyandlin profile image
paddyandlin in reply to

that is great hope it goes well?

SueLovett profile image
SueLovett

This is amazing especially as I witnessed a young doctor telling a medical student that APS is 'very very rare'! He also informed his young friend that it was 'something that caused tiny clots'!

I think I put him right on a few things but would have liked more time.!

I gave him a couple of handouts on Hughes which he grudgingly accepted and then placed on the desk without opening them. This arrogance holds us back.

Thank goodness for the Hughes Fondation and it's members for bringing it to people's attention.

Well done Kate and All x

Lesley_D profile image
Lesley_D

Amazing, and such a strong group full of caring people

Lesley

x

jessielou profile image
jessielou

Thats great. Mmmmm very rare condition. I think not!!!!

Love n hugs sheena xxxxx not:-) :-) :-)

Not what you're looking for?

You may also like...

Here we go again...

Hi everyone, I'm pregnant again! 7 weeks, just had a scan and it's just one this time thank...

where do i go from here????

Hi all today i received my blood test results and both were negative. im not sure where to go...
linda1scot profile image

Well, we are now well over 5,000 members on here

Thank you for all the great feedback you send us Administrators, both out here and by private...
MaryF profile image
Administrator

We do NOT have APS. We have AUTOIMMUNITY!

I've been seeing a number of posts lately regarding unfortunate experiences with doctors, poor...
TheKid profile image

New here

Hi, I live in the US (Texas) and was diagnosed with APS/Hughes in 2011 after a series of surgeries,...
junipers76 profile image

Moderation team

See all
lupus-support1 profile image
lupus-support1Administrator
KellyInTexas profile image
KellyInTexasAdministrator
HollyHeski profile image
HollyHeskiAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.