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Latest News from Prof Hughes! Yep! Lupus-Sjogrens-Hypothyroid dis. My hip. AND the cold weather hurts me.!!
Hi folks, Before christmas i wrote that i was seeing the Lupus legend Prof G Hughes at London Bridge Hospital... see here: http://lupusuk.healthunlocked.com/blogs/93247/Im-going-to-see-ProfGraham-Hughes-on-thursday Well, he was great. Turns out that indeed i obviously had childhood Lupus and
Hi folks, Before christmas i wrote that i was seeing the Lupus legend Prof G Hughes at London Bridge Hospital... see here: http://lupusuk.healthunlocked.com/blogs/93247/Im-going-to-see-ProfGraham-Hughes-on-thursday Well, he was great. Turns out that indeed i obviously had childhood Lupus and
faeryfey
in
LUPUS UK
13 years ago
Hi all anyone had hip replacement operation with FM would love to hear how you got onsue x
sue247
in
Fibromyalgia Action UK
12 years ago
fibro flare
having a really rough time at moment, not long been diagnosed and still getting head round all the crap stuff we go through but over last few weeks have been having a major flare up. hubby has just had a hip replacement op and so am trying to look after him and the house and 2 teenagers who forget they
having a really rough time at moment, not long been diagnosed and still getting head round all the crap stuff we go through but over last few weeks have been having a major flare up. hubby has just had a hip replacement op and so am trying to look after him and the house and 2 teenagers who forget they
wanita2k
in
Fibromyalgia Action UK
12 years ago
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Getting Nervous now
Well only 4 days to go till hip replacement operation, so much to do and not enough energy to do it. ! not looking forward to getting back after op not being able to do anything much, and the swollen legs etc Not to mention my hands and wrists are so weak and painful worried about crutches although my
Well only 4 days to go till hip replacement operation, so much to do and not enough energy to do it. ! not looking forward to getting back after op not being able to do anything much, and the swollen legs etc Not to mention my hands and wrists are so weak and painful worried about crutches although my
sue247
in
Fibromyalgia Action UK
12 years ago
Hi everybody new to this site
Well as I said new to this site but sadly had FMS since 1993 I found this from the nhs choices web site and was immediately drawn to reading the blog's. I have just returned from yet another hospital appt as usual feeling what's the point..., you know how it goes more tests on the way. I do now have
Well as I said new to this site but sadly had FMS since 1993 I found this from the nhs choices web site and was immediately drawn to reading the blog's. I have just returned from yet another hospital appt as usual feeling what's the point..., you know how it goes more tests on the way. I do now have
sue247
in
Fibromyalgia Action UK
12 years ago
Here we go again!!!! Just what can I do.....
I have had Lupus for 26 years and apart from the first few years and my times having my children, two miscarriages, followed by losing my first baby at 4 days old but going on to have another son and daughter, lupus has been quite kind to me. Now in my early 50s I seem to have problems all day and night
I have had Lupus for 26 years and apart from the first few years and my times having my children, two miscarriages, followed by losing my first baby at 4 days old but going on to have another son and daughter, lupus has been quite kind to me. Now in my early 50s I seem to have problems all day and night
schnauzersmudge
in
LUPUS UK
13 years ago
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