Posts - LUPUS UK | HealthUnlocked

LUPUS UK

31,597 members28,006 posts

All posts for April 2012

Are there any teachers (or trainee teachers) with Lupus out there?

Hi there, I was diagnosed with Lupus last september after having symptoms but...
heidieidi profile image

Oh hi! Nervous System Flare I assume? How nice to meet you! How long will you be staying???

I'm pretty sure I'm having some nervous system issues. This last month has been ...
Blueberry profile image

really bad day !!!!!

what a shitty day ive had ! had my ESA stopped cos it was contribution based and...
normajean profile image
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Very Achy Thigh and Knee Pain !

Can anyone tell me if they have achy thighs and knees a lot, as i have been on a...
Hidden profile image

Has anyone else experienced urinary/bladder discomfort as part of a flare?

I haven't so far had any organ involvement, so when I was in bed with a recent f...
Maya23 profile image

My Dr. says I have Lupus after my bloods came back saying so and that I don't have Rheumatoid,

But I went to my Rheumatoid Dr and he say's I don't have lupus but I do have Rhe...
Debbee profile image

Scratching my arms + thighs belly back little raised bumps antihistamine helps is there other ways 2 help. Its worse at night

Would like to know im not only one suffering with this its worse at night and so...
shells profile image

Azathioprine

Hi, all I'm waiting for results of blood work to see if i can take Azathiopri...
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not quite diagnosed?

Hi there, I am 41 and have been sick most of my life. I can remem...
SherrieP profile image

Middle aged fog?

When you're middle aged, how can you tell if it's Lupus Fog or the usual Midd...
janetd profile image

I won the tribunal

I am glad to say after 6months of driving myself mad we won the tribunal. I was ...
NiksB profile image

Feel. Down and alone

Went to docs other day waste. Of time saw a locomotives l went with my list. Suf...
suemac profile image

Recently diagnosed with APS......help! need some advice

Hi i have recently been diagnosed with SLE after being treated for the last 3 ye...
jani4063 profile image

Does anyone with SLE suffer with Hypochondria/paranoia? My latest symptoms are breathlessness and lumps around my jaw, what have I got now??

I've been diagnosed now for a couple of years, but like most have suffered for y...
Acorn1 profile image

hello, im new to this site

hi my name is jayne, im new to this site firstly is there anyone around the glou...
jaynemolz profile image

My first lupus blog

hello everyone,i was unsure to join a site like this as ive spent alot of time o...
poodlegal profile image

Does anyone else suffer from the skin round the base of fingernails splitting, is this due to the lupus or a side effect of

hydroxychloroquine or methotrexate
lupydragon profile image

My duaghter in law died of SLD, should her daughter who is 19 be checked?

Benjamin profile image

Hello. Im New on this site...

Hello, Im Linda and i have LUPUS for over 28 years.. Im Born in The Netherland...
Lovelylin profile image

A modern petition for cash strapped times

I have had some great care and some awful care for both myself and my children o...

Press statement on NICE’s Announcement on Belimumab

LUPUS UK is extremely disappointed that NICE has refused to recommend Belimumab ...
Paul_Howard profile image
Partner

An article from today's papers

I have also loaded this up on the Hughes Syndrome Foundation forum, due to membe...
MaryF profile image

Family ignorance !

Iwas wondering how do other Lupies cope when family members just (dont get it !!...
larissa profile image

is this part of Lupus !!!??

I've had a rash on my ankle for about a week now , its red and raised ( bumpy to...
larissa profile image

This Really helped me

I've just joined the group - I'm in the midst of a flare up because I ignored th...
Chuni profile image

I FINISHED THE LONDON MARATHON!!!!!

I ran it all and enjoyed every second of it. I would just like to say Thank You...
tracey_edey profile image

Is there a link between Spondylitis & Lupus

After some tests today on the nerves in my arm, the consultant Neuro physiologis...
tidmusshaz profile image

Has anybody had a EMG investigation of the muscel and nerves as part of a diagnoses of lupus?if so was there anything conclusive .

.
Poppygayle profile image

Turning myself more and more inwards and feeling invisible.

This is my first blog post. I've still not seen a Rheumy due to my GP letting me...
Blueberry profile image

Not sure there is really a point to me being here anymore

Not sure where to start. Have had Lupus for 20 years so quite used to the ups an...
RebeccaAnn profile image