Lupus Trust
@lupustrust
The Lupus Trust was set up as a registered charity in 1991. Its aim is to support lupus research at Guys Hospital & raise lupus awareness.
ID:525498869
http://www.lupus.org.uk 15-03-2012 16:02:23
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As I get older and get more aches and pains the harder it is to remember what it was like when I had no pain at all.
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #chronicnotebook
Sadly true. π«€
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #lupus truth #lupus facts
If you think you may have lupus but are having difficulty getting a diagnosis our article 'what to do if you think you have lupus but can't get a diagnosis' may help: lupus.org.uk/.../what-to-doβ¦...
#WorldLupusDay #chronicpain #autominnunedisease #invisibleillness #lupusfact
When you tell people that you have lupus they sometimes don't understand that lupus is infact a chronic often debilitating disease with (currently) no cure and is sometimes even fatal.
#WorldLupusDay #Lupus #lupustrust #lupusfact
For me this is exactly right. not one person knows when I get very sick. I prefer to stay at home in the peace and quiet and recover until I feel well enough to interact with people again.
#lupus #lupus trust #lupus awareness #chronicillness #chronicpain
Made me laugh as it's totally accurate!! π
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #lupus truth #lupus facts #doctorsappointment
As members of the Prescription Charges Coalition, weβre joining The PDA, National Pharmacy Association, RCGP, Royal Pharmaceutical Society in calling for an urgent review of the exemption list for prescription charges in England.
Find out more-
prescriptionchargescoalition.co.uk #ReviewTheList #lupus
It always saddens me when I see people post that they feel they're a burden. We didn't ask for lupus and we didn't deserve it, so remember these words.
#lupus #lupus trust #lupus awareness #chronicpain #chronicillness #invisibleillness #autoimmunedisease #lupus warrior
It's no wonder we sometimes fell like this, we put up with a lot & for the majority of the time in silence. π
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #lupus truth
Lupus in a nutshell! π
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #lupus truth #lupus facts
This happened to me recently and I reacted exactly the same way π
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #lupus truth #lupus facts
I find myself trying to negotiate with my body saying 'I know there has to be some pain, but could it be a bit less than this?'
#chronicpain #autominnunedisease #invisibleillness #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness
And so they should!
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness #lupus truth #lupus facts
Very true, it's exhausting explaining over and over why you aren't 'better yet' or how 'yes, you're still in pain'.
#chronicpain #autominnunedisease #invisibleillness #lupus fighter #LupusSucks #chronicillness #LupusLife #lupus warrior #lupus #lupus trust #lupus awareness
I start a story, lupus brain fog kicks in and I can't remember where the heck I was going with it, so I just keep going in the hope I'll eventually remember. π
#lupus #lupus trust #lupus awareness #brainfog #lupus brainfog #chronicillness #autoimmunedisease #chronicpain