Posts - LUPUS UK | HealthUnlocked

LUPUS UK

31,918 members28,241 posts

All posts for April 2013

Been turned down for DLA and ESA now!!!!

Whilst I appreciate that the government doesn't have an open money pot to hand o...
beckybooboo profile image

Oh God, it doesn't half hurt today.

Not having a very good day, hurting, better half in hospital (poisoned legs n br...
jayniey profile image

Plaquenil and Quinoric

50 year old male have been on Plaquenil since 1989 have noticed that since I sta...
Liberton profile image
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Please,please anybody tell me what to do now

my arms and legs are killing me I feel sick and sweating but no temperature. Thi...
letslaugh63 profile image

A long, hot, sticky night in flares, & I don't mean down the local disco for a 70's extravaganza.

I've always had night fevers & achy joints when my lupus flares, but last night ...
roobarb profile image

Sheffield Lupus Group first ever meeting :)

Hi All :) After having to postpone our first meeting in March due to horrible...
Silvermyst profile image

has anyone else lost babies due to their lupus and gone on to have a 'successful' pregnancy?

im just wondering what to expect from my 'pre-conception' appointment and i am m...
mummybumble profile image

IV steroid drip

Hi everyone, hope you all had a good day, I did today and took my babies to the ...
amandamummy profile image

I have Lupus (sle) but also have other autoimmune illness's but doctors have'nt a clue about me,Is there any1 else in same situation?

I have been steroids for nearly 7yrs now which have caused me to break my hip tw...
Lisa78 profile image

Reference Pregabalin withdrawal - again!!

I've found amitriptyline along with dihydrocodeine (if u don't object to a bit (...
jayniey profile image

London Lupus suffers-April meeting date??

I recall that some London members had a meeting a little while ago and were talk...
bam1993 profile image

breathlessness , anyone ????????

i have been suffering from breathlessness for a few years now, but these last fe...
rockchic profile image

Anyone interested in starting a nutters club?

I propose Sher 78 as the Chairperson. I'd join, I could do with a good laugh. L...
jayniey profile image

SLE for sale!!!!

Any takers, I can throw in pregabalin withdrawal 4 free if u like? I could even ...
jayniey profile image

Confused!

I've been recently diagnosed. 8 weeks and 2 days to be exact, and I still don't ...
E-Say profile image

Why don't they get it?

I'm going nuts over here, I'm fed up with people making me feel like a hypochond...
Lupdaloop profile image

Pregabalin withdrawal and hallucinations getting worse!

My skin is now raw, blistered and swollen. Lost a tooth this morning. Docs offer...
jayniey profile image

Mycophenalate side effects?

I have just increased my dose and and soooo tired but not like my usual Lupie fl...
DaleDiva profile image

Problems

Im having pains in my lower back, chest pain underneath my right breast, headach...
Danielle2419 profile image

went for rheumy on monday

hiya all hope you all feeling not to bad i had a appointment on tuesday i have 2...
else5 profile image

Young and coming to terms!

Hey I have SLE for over 3years It became active at 19 and I was diagnosed at 21 ...
shay1 profile image

Hi everyone. Does any body know if there is any LUPUS group meetings in or near Warrington. thanks. x

gazzasoens profile image

Is this usual?

I'm fed up! Is it usual to feel er.......er.......crap! Sorry can't think of ano...
talula profile image

Copper/magnetic bracelets

Has anyone used either copper or magnetic jewellery and have they found any bene...
Jaxqueline profile image

Hi guys, I'm back asking for another favour haha!

Thank you all soooo much for voting for my cupcake bouquet last month, unfortuna...

have a laugh on me

I thought I was doing well today and decided to do a roast dinner, I put the mea...
luupysue profile image

thought it was going to well....

after my previous posts my body decides to go mad again, developed the worst hea...
scoobydoo1 profile image

Went to my first Lupus Group meeting.

I went to my first Lupus group meeting last saturday, it was held at a local gar...
T3KAO profile image

Mononeuritis Multiplex

Does anyone have Mononeuritis Multiplex as a complication of SLE? If so what tr...

Lupuzor anyone?

Just been doing some digging on meds,thanks to reading other people's blogs and ...
Lupdaloop profile image