Posts - LUpus Patients Understanding and Support | HealthUnlocked

LUpus Patients Understanding and Support

3,419 members • 1,257 posts

All posts for October 2014

PIP

There has been a lot of talk, quite rightly, about PIP claims. I have Lupus, osteoarthris, a recent hip replacement (I am getting the other one done and both...

There has been a lot of talk, quite rightly, about PIP claims. I have Lupus, os...

•9 years ago

Red and Dry

My eyes every time I sleep at midnight It is red and dry, and it feels like there is sand in it. Why is this happening?

My eyes every time I sleep at midnight It is red and dry, and it feels like ther...

•9 years ago

Let's get talking!

Hi all, I don't know about you but I'm having a pretty rubbish day. I started on methotrexate last night and so far I'm too tired to move. I feel like I've...

Hi all, I don't know about you but I'm having a pretty rubbish day. I started o...

Volunteer•10 years ago

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Let's get talking! Sending hugs!

Hi all, I don't know about you but I'm having a pretty rubbish day. I started on methotrexate last night and so far I'm too tired to move. I feel like I've...

Hi all, I don't know about you but I'm having a pretty rubbish day. I started o...

Volunteer•10 years ago

Muscle twitching!?

Hi all, I was wondering if any of you have muscle twitching with their lupus? I know it's not a common symptom so obviously starting to worry its something...

Hi all, I was wondering if any of you have muscle twitching with their lupus? I ...

•10 years ago

A quick question

I have been diagonisrd with conective tissue disease and fibro ( positive ana speckled, positive anti RNP and DsDna). I am on plaquenil 200 mg per day and...

I have been diagonisrd with conective tissue disease and fibro ( positive ana sp...

•10 years ago

Scared mother SLE?

Hi all, I've just joined and been reading some of your posts and your all pretty fab how your dealing with things, me? Not so much!. I got poorly in May, it's...

Hi all, I've just joined and been reading some of your posts and your all pretty...

•10 years ago

Looking for new lupies for mutual support and understanding!

Hi there, I'm Suzy, I'm 23 and I've had Lupus for 12 years, I was diagnosed when I was 11 and was in the last stage of kidney failure. I was diagnosed with...

Hi there, I'm Suzy, I'm 23 and I've had Lupus for 12 years, I was diagnosed wh...

Volunteer•10 years ago

Bullying Culture in NHS Mental Health Services Putting Vulnerable Patients at Risk

Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are...

Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEA...

Administrator•10 years ago

I stopped taking my lupus medication, I feel fine, how do I tell my Rhematologist?

Hello, I was diagnosed with Lupus two years ago. When I was first diagnosed the only symptom I had was joint pain, Rheumatologist Diagnosed me with lupus...

Hello, I was diagnosed with Lupus two years ago. When I was first diagnosed the ...

•10 years ago