Behcets and lupus : Hello does anyone have a... - LUPUS UK

LUPUS UK

31,744 members28,102 posts

Behcets and lupus

donna profile image
16 Replies

Hello does anyone have a diagnoses of Behchets diesease to add to their Lupus SLE?

Written by
donna profile image
donna
To view profiles and participate in discussions please or .
Read more about...
16 Replies
lynzard profile image
lynzard

Hi there

Relly sorry, never heard of it. Will have a good old google. Take care

joannebond360 profile image
joannebond360

Been told I have characteristics of both diseases.

joannebond360 profile image
joannebond360 in reply to joannebond360

You can get a cross over between both

donna profile image
donna in reply to joannebond360

Hi thank you for replying to me .sorry to hear you have a cross over..there seems to be a lot of info left on my original question now so l hope you will get some help information to xxx bestwishes Donna xx

caz59 profile image
caz59

Hi donna. can you describe what Bechets is please, never heard of it.

donna profile image
donna in reply to caz59

Hi caz59 , thanks for leaving a reply.there seems to be quite a few explanatory replies to my question now so I hope you will find them as helpful as me ..I know what my symptoms are ,but now reading so much has linked a lot more together..the never ending diagnoses puzzle! Bestwishes Donna

Hi Donna, i was diagnosedwith Behcet disease and Sjogren,raynald last year. This year with SLE.If i am right someone correct me if i am wrong please, but Behcet is to do with inflamation of the arteries and blood vessels. I think Rheumy told me last year i have it at back of my eye and if i am right it can also be called vasculitis of the eye! Not sure on that but maybe someone on this forum can put me right! It is a rare disorder of the immunity. I callapsed with it last year. I see the eye clinic every 3 months and so far its stable and not active, the main artery behind my eye.

donna profile image
donna in reply to

Hi smurfette43 thanks for your reply..I'm sorry to hear your having such a rough tome with it all x hope things settle own for you very soon xxx bestwishes Donna x

tracynoe profile image
tracynoe

Behcet's is a rare form of Vasculitis and can cause a huge array of problems and symptoms there is a dedicated section of healthunlocked for Vasulitis UK

donna profile image
donna in reply to tracynoe

Thanks tracynoe for pointing me to the vasculitis UK HU forum..didn't make the link myself..bestwishes donna

RichardE profile image
RichardE

Hi everyone.

As smurfette43 and tracynoe say, Behcet's is a form of Vasculitis - an autoimmune disease causing inflammation of the blood vessels. Some types are similar to Lupus and people with SLE can sometimes have Vasculitis as a secondary condition.

As well as our HealthUnlocked page we have some more information on Behcet's and the other types of Vasculitis on our website :

vasculitis.org.uk/about-vas...

By the way Vasculitis UK have been invited to have a stand at the Cambridgeshire branch of Lupus UK's information day next month. So if any of you are coming along to that event please say hello.

Richard,

Vasculitis UK.

donna profile image
donna in reply to RichardE

Hello Richard ,thank you for taking the time to reply to me about the Bechets and linking to the vasculitis website.. more reading! and learning.i will also check out the HU forum..as I mentioned I haven't been diagnosed as yet with Behcets but my GP believes it is what's going on...there is certainly a new twist to my symptoms..never a dull moment!

Bestwishes Donna

RichardE profile image
RichardE in reply to donna

You're welcome Donna. Do shout if you have any questions about Vasculitis and I'll try my best to help.

Oh and your GP sounds pretty switched on to autoimmune diseases. In our experience GPs often know little to nothing about Vasculitis !

All the best,

Richard.

in reply to RichardE

To Richard.I would be very interested to go. Where can i find out the information and place where it will be held and the time? As i will have to arrange child care.Thanks for letting us know.

RichardE profile image
RichardE in reply to

The Cambridgeshire Group of LUPUS UK has organised this event for the 12th October 2013 at the Wellcome Trust Conference Centre, Hinxton, Cambridge.

I believe that the event has proved very popular and I think they now have a waiting list for places. But if you contact Shelagh Cheesman via mail@cambridgeshirelupus.org.uk she will be able to let you know the current position for places.

Mainshah profile image
Mainshah

RichardE your right there my gp now as little as I did lol, she dint nw what was going on with me so suffered for 4 weeks with aches and pains and stayed in a flare up for that long until I cunt walk a few steps to the bathroom, due to a rash on my legs an over sized / swollen feet.

Took matters in my own hands then went to hospital and with in a week was diagnosed with lupus SLE.

GPS now very helpfull and keeps a good eye on me

You may also like...

Lupus or not lupus?... That is the question...

but can anyone advise on whether this will change? Did anyone else find out they had lupus via...

Relationships and Lupus

Why don't you have a boyfriend? Aren’t you lonely? Don’t you want to get married and have kids? I...

antibiotics and lupus

Hi I have been diagnosed with lupus and take pacquenil. The winters are tough and I took penicillin...

👣👣👣👣👣👣👣👣👣👣👣👣👣👣👣LIFE WITH LUPUS👣👣👣👣👣👣👣👣👣👣👣👣👣👣

not a normal guy). We have to laugh and make the best we can when we have Lupus. So Crusee I saw...

The Lupus Encyclopedia

here about lupus, sweating & the autonomic  system, George posted a great excerpt from The Lupus...