linking to APS on the web: Hi All I... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,330 members10,524 posts

linking to APS on the web

suntap profile image
3 Replies

Hi All

I notice several of you advocate and educate others about Hughes Syndrome.  I have a website for my business and wondered it I could put a link to the charity website?  Or is this not the done thing?  I don't want to step on anyone's toes.

Also, is there a succinct paragraph stating what Hughes is and some of its symptoms that I could also put up?

Thanks for all your great work.

Di.

Written by
suntap profile image
suntap
To view profiles and participate in discussions please or .
3 Replies
MaryF profile image
MaryFAdministrator

Hi, if you contact the charity, I am sure they can help you with that. Best wishes. MaryF

suntap profile image
suntap in reply to MaryF

Thanks Mary

tim47 profile image
tim47

I used to have  a couple of active websites completely unrelated to Hughes and I used to include a link to HSF  amongst my 'other links' simply to spread the word. I also linked to  a few other sites of interest that I supported.

You may also like...

Anyeurisms and APS? Are they Linked?

Abdominal aeortic anyeurism. The aeortic arch was also involved. Dacron was used to replace parts...

APS and links to other conditions

but do read all the posts. I’ve read a lot recently about other conditions and the link to APS. My...

Is APS linked to other immune issues?

others. E.g my Igg is high but also my Ige is very high (allergies). I wonder if these others are...

Osteoneocrosis link to APS

systemic corticosteroids \\" All these years I haven't been able to put a reason down to my...

APS and Lupus Genetic link?

it seems the most likely thing to me. And, if I have lupus \\"like syndrome\\" can that progress...