Posts - Behçet's UK | HealthUnlocked

Behçet's UK

5,243 members4,329 posts

All posts for November 2013

London to Paris fundraiser for the Behcet's Syndrome Society

So we've booked the Adventure Company, we have the route planned, now all we nee...
BSSAdmin profile image

Is most everyone with Behcet's on some type of an immunosuppressant long-term? What is your experience? Thanks

(One doctor wants me on azathioprine for two years to settle down my system and ...
Rose138 profile image

On for the kiddies ( click or copy and paste link and follow instruction )

http://www.portablenorthpole.com/home?emst=wak79o8cUI_614287_39568_24&utm_campai...
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Is hair loss common in this disease? Or is it my Hashimoto's acting up again? It's bad enough I feel like hell. do i have to be bald too?

freckles66 profile image

LEG PAIN WHEN WALKING

I will try and describe this the best I can. I am having to rely alot now on usi...
pheobe67 profile image

Leicester Support Group meeting Change of Date

We have had to rearrange the date for the next Leicester support group meeting d...

London Support Group Reminder

Hi there, Just wanted to remind everyone that there will be a group held on Thur...

1st flare up in two & half months after stabilised on infliximab infusions !

Hi , everyone ... not been on here for a while - dont worry not forgotten you :-...
SignalBoxer profile image

Heart beating fast.

Hi new on here ,does any one else have problems with their heart beating very lo...
happyhacker56 profile image

my son is worse because of drugs does it get better

lottie01harry profile image

Hi I have just heard from someone else who has behcets that there is a specialist who comes to the UHW in cardiff once a week on a Thursday

Just wondering if any one else knows if this is right ? X
Jackamo profile image

HI. I'm new here!

My name's Bliss. I'm Canadian Eh? I live in a teeny tiny town in an area of Bri...
blissaru profile image

esa stopping in april, due to contributions running out, husband works so been told i will get nothing. is there anything else i can claim

my esa i recieve is from when i worked full time. i lost my job due to behcets a...
millie11 profile image

Dr. Yusuf Yazici

I've been referred to him by my local dr I've seen Dr Yazici once so this Tuesda...
Nicole86 profile image

Sleep

So for a couple months now I have not gotten a good nights sleep. I've tried lu...
Nicole86 profile image

Hello everyone! I'm new here and looking for support and info on bechets disease! I was diagnosed in February 2013 and it's awful

I've tried prednisone and colcrys and humira injections but nothing has helped. ...
Nicole86 profile image

London Support Group: December

Our next meeting will be held on Thursday 12 December, 3-5 pm at the: Centre for...
Hidden profile image

Is anyone else recieving e-mails via health unlocked from a lmfc .i thought our information was restricted to this site.......

It may be a troll...someone who has registered to gain access.its not pleasant t...
Oceanna profile image

Suspected Behcet's... Any advice?

Hi all, I was diagnosed with CFS/ME back in 2000, but never thought it was the w...
Jaxxi profile image

Back Surgery?

has anyone had any sort of back surgery? I am looking at lower back surgery to c...
Dmartin138 profile image

Positive comments!!!

Hope everyone is doing alright. Mild flare up at the moment. Just wanted to post...
Dmartin138 profile image

Cambridge Vasculitis Support meeting on 7 December

The Behcet's East of England support group is linking with the Vasculitis group ...
Zebra profile image

Am atm suffering from what feels a never ending headache... :-(

am on day 6 of constant pounding n throbbing head, eyes burning,blury and sensit...
nickyclem profile image

Hi all went to c my rheumatologist today an she know says I have fibromyalgia as well as the bechets an everything else just wondering if

Anyone else has this if so how do u manage it thanks all xx
Jackamo profile image

how do I claim any money/benefits as ive left my job due to my illness

17months have passed and to be honest im no further forward, still having ulcers...
evo74 profile image

i have this weird burny, throbby dizzy feeling in my spine and head. almost always. does anyone else deal with this?

freckles66 profile image

I feel badly that I'm earning "frequent flyer miles" so to speak with all my many recent questions, but if I may ask one more for now: Does

it seem rather extreme that my rheumatologist would pull me off Imuran and tell ...
Rose138 profile image

Just wanted say hello formally and anyone else in USA. If not where are you from?

Title describes it. My name is Dean. I'm from San Diego, CA. seems medicines in ...
Dmartin138 profile image

ACNE

when you guys break out with any sort of acne does anyone else feel after they h...
Dmartin138 profile image

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