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Imagery for the relaxation- much needed after yesterdays jaunt!
Morning all my friends :D Hope you are all rested and not aching or hurting too much from yesterdays escapades :o I know I am and I spent most of the day chasing fluffies, baddies and trying to escape the naughtiness of those whom shall remain nameless............ you know who you are heheheheheh!
Morning all my friends :D Hope you are all rested and not aching or hurting too much from yesterdays escapades :o I know I am and I spent most of the day chasing fluffies, baddies and trying to escape the naughtiness of those whom shall remain nameless............ you know who you are heheheheheh!
Hidden
in
Fibromyalgia Action UK
11 years ago
New NICE Guidance released.
The Department of Health has asked the National Institute of Health and Care Excellence (NICE) to produce guidance on using topotecan, pegylated liposomal doxorubicin hydrochloride, paclitaxel, trabectedin and gemcitabine in the NHS in England and Wales. The Appraisal Committee has considered the evidence
The Department of Health has asked the National Institute of Health and Care Excellence (NICE) to produce guidance on using topotecan, pegylated liposomal doxorubicin hydrochloride, paclitaxel, trabectedin and gemcitabine in the NHS in England and Wales. The Appraisal Committee has considered the evidence
SoniaOvacome
in
My Ovacome
11 years ago
Have you taken Xarelto (rivaroxaban)?
Another request - please get in touch if you can relate to this and live in the UK: - We are looking for someone with AF who is willing to tell their story to the media and be photographed. Ideally they would be on warfarin or aspirin and have been refused a novel oral anticoagulant (dabigatran, rivaroxaban
Another request - please get in touch if you can relate to this and live in the UK: - We are looking for someone with AF who is willing to tell their story to the media and be photographed. Ideally they would be on warfarin or aspirin and have been refused a novel oral anticoagulant (dabigatran, rivaroxaban
AFAssociation1
in
AF Association
11 years ago
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Referred to specialist unit
I have been waiting for the results of a liver biopsy since May-largely because the pathologist was off sick/on holiday and no-one knew whether or not I needed treatment for AIH overlap. I was diagnosed with PBC some 20years ago and had become a bit complacent because although I appear to have some of
I have been waiting for the results of a liver biopsy since May-largely because the pathologist was off sick/on holiday and no-one knew whether or not I needed treatment for AIH overlap. I was diagnosed with PBC some 20years ago and had become a bit complacent because although I appear to have some of
crundalite
in
PBC Foundation
11 years ago
I have had a high anti nuclear factor of 340, TSH fluctuating between 3.8-5.8, FT4 12.8. I have intermittent joint pain in fingers, hairloss
I have brain fog. I have see two rheumatologists who say my results are boarderline therefore I cannot be treated. I have been given a script for an antimalarial tablet. I don't feel normal but I am getting no where. Any thoughts?
I have brain fog. I have see two rheumatologists who say my results are boarderline therefore I cannot be treated. I have been given a script for an antimalarial tablet. I don't feel normal but I am getting no where. Any thoughts?
Frazzie1
in
Thyroid UK
11 years ago
PBC
Just found out that I'm AMA positive. My symptoms are itching and slight pain on my right lower rib. If you're AMA positive, does it mean you have PBC? I have read too much regarding PBC and I'm very worried and scared. My husband told me to be positive and I'm trying to.
Just found out that I'm AMA positive. My symptoms are itching and slight pain on my right lower rib. If you're AMA positive, does it mean you have PBC? I have read too much regarding PBC and I'm very worried and scared. My husband told me to be positive and I'm trying to.
barotacnuevo
in
PBC Foundation
11 years ago
Great North Fun Revisited
A day has gone by and the excitement has died down. My personal congratulations to everyone to attempted the GNR - and especially to those who got to the finish under their own steam. I seem to have created some excitement by blogging as I went along. In reality, it was a couple of posts at the start
A day has gone by and the excitement has died down. My personal congratulations to everyone to attempted the GNR - and especially to those who got to the finish under their own steam. I seem to have created some excitement by blogging as I went along. In reality, it was a couple of posts at the start
Malcy
Graduate
in
Couch to 5K
11 years ago
Zoloft and Ativan
Hi, anyone take the antidepressant Zoloft and the anti-anxiety drug Ativan. I'm taking both to try and get rid of my wretched Depression. Stay well. Martin
Hi, anyone take the antidepressant Zoloft and the anti-anxiety drug Ativan. I'm taking both to try and get rid of my wretched Depression. Stay well. Martin
martin1945
in
Lung Conditions Community Forum
11 years ago
Anyone on here NOT on Urso for their PBC? How are your LFTS with NOT being on this medicine?
I went off the Urso last year as a last resort as I had had a horrendous year with the itch( much like yr had before was diagnosed) . I had read an article about a new drug being trialed for PBC and it mentioned that quite a few of the participants who had never had ich from their PBC complained of
I went off the Urso last year as a last resort as I had had a horrendous year with the itch( much like yr had before was diagnosed) . I had read an article about a new drug being trialed for PBC and it mentioned that quite a few of the participants who had never had ich from their PBC complained of
littlemo
in
PBC Foundation
11 years ago
dry and thinning hair
hello , i have been taking methotrexate , 15mg weekly , hydroxychloroquine 2 tablets daily and 1 folic acid tablet weekly which have helped me greatly my problem is now iv got thin and very dry hair and was wondering as anybody got any advice to help me with this problem thank you Lorraine
hello , i have been taking methotrexate , 15mg weekly , hydroxychloroquine 2 tablets daily and 1 folic acid tablet weekly which have helped me greatly my problem is now iv got thin and very dry hair and was wondering as anybody got any advice to help me with this problem thank you Lorraine
lorrain
in
NRAS
11 years ago
Does Prednisolone make your hair fall out?
I could thatch a roof with what I have left every time I brush my hair, I didn't have this problem before and my hair feels a lot thinner to the touch, it used to feel quite thick. I don't have any bald patches (yet!) I'm getting quite worried about the amount of hair loss, it seems to have got worse
I could thatch a roof with what I have left every time I brush my hair, I didn't have this problem before and my hair feels a lot thinner to the touch, it used to feel quite thick. I don't have any bald patches (yet!) I'm getting quite worried about the amount of hair loss, it seems to have got worse
DazedAndConfused
in
PMRGCAuk
11 years ago
Shall I ring my rheumy nurse?
Hi all . Not been posting but reading all yours daily. Well I changed to sulfasalizine and mtx about 3 months ago and I thought this is it, as I felt loads better and nearly normal. Well started to flare again about 2 weeks ago and this last week have felt dreadful. Flares happening every couple of
Hi all . Not been posting but reading all yours daily. Well I changed to sulfasalizine and mtx about 3 months ago and I thought this is it, as I felt loads better and nearly normal. Well started to flare again about 2 weeks ago and this last week have felt dreadful. Flares happening every couple of
BossyB
in
NRAS
11 years ago
August's Blog Post - Smartphone apps to help manage aspects of your lupus
The latest figures show that around 7 in 10 people in the UK own a smartphone. There are billions of apps available to download, which have an almost endless range of uses. With help from people on the LUPUS UK Facebook page and our HealthUnlocked community, I've pulled together a short list of some
The latest figures show that around 7 in 10 people in the UK own a smartphone. There are billions of apps available to download, which have an almost endless range of uses. With help from people on the LUPUS UK Facebook page and our HealthUnlocked community, I've pulled together a short list of some
Paul_Howard
LUPUS UK
in
LUPUS UK
11 years ago
my inr is 1.6 warfarin dose is 10 should I still be having fragmin injections no one can make their mind up
I was told originally to carry on having injections until inr stabalised at 2.5
I was told originally to carry on having injections until inr stabalised at 2.5
webbie
in
Anticoagulation Support
11 years ago
Daily Laughter Wednesday
Daily Laughter Wednesday May I first thank you all for responding to my call yesterday. I thought that I was wearing the wrong aftershave and everybody was staying clear of me, but as usual the friends on this site put me at ease. Thank you so much, every now and again I loose the plot. xxxx The
Daily Laughter Wednesday May I first thank you all for responding to my call yesterday. I thought that I was wearing the wrong aftershave and everybody was staying clear of me, but as usual the friends on this site put me at ease. Thank you so much, every now and again I loose the plot. xxxx The
Hidden
in
Lung Conditions Community Forum
11 years ago
Acceptance
I have been so depressed lately and have had a couple of meltdowns (one at Walmart and one with my Neuro). I decided the most important thing I can do for my emotional well being, in addition to Paxil, is to quit thinking about "what was". I came across this poster and thought it very fitting so I printed
I have been so depressed lately and have had a couple of meltdowns (one at Walmart and one with my Neuro). I decided the most important thing I can do for my emotional well being, in addition to Paxil, is to quit thinking about "what was". I came across this poster and thought it very fitting so I printed
tlongmire
in
Cure Parkinson's
11 years ago
Acceptance
I have been so depressed lately and have had a couple of meltdowns (one at Walmart and one with my Neuro). I decided the most important thing I can do for my emotional well being, in addition to Paxil, is to quit thinking about "what was". I came across this poster and thought it very fitting so I printed
I have been so depressed lately and have had a couple of meltdowns (one at Walmart and one with my Neuro). I decided the most important thing I can do for my emotional well being, in addition to Paxil, is to quit thinking about "what was". I came across this poster and thought it very fitting so I printed
tlongmire
in
Cure Parkinson's
11 years ago
Acceptance
I have been so depressed lately and have had a couple of meltdowns (one at Walmart and one with my Neuro). I decided the most important thing I can do for my emotional well being, in addition to Paxil, is to quit thinking about "what was". I came across this poster and thought it very fitting so I printed
I have been so depressed lately and have had a couple of meltdowns (one at Walmart and one with my Neuro). I decided the most important thing I can do for my emotional well being, in addition to Paxil, is to quit thinking about "what was". I came across this poster and thought it very fitting so I printed
tlongmire
in
Cure Parkinson's
11 years ago
Festivals
Hi everyone, I am in need of some advice. I have managed to get hold of a lsat minuet ticket for V Festival ( my friend selling it). I have never been to a festival before but have always wanted to go. But I am a bit worried how my chest will be. My asthmas is difficult to control and have had ITU
Hi everyone, I am in need of some advice. I have managed to get hold of a lsat minuet ticket for V Festival ( my friend selling it). I have never been to a festival before but have always wanted to go. But I am a bit worried how my chest will be. My asthmas is difficult to control and have had ITU
Hidden
in
Asthma Community Forum
11 years ago
Tinea versicolour
Does anyone else have this condition or have any tips on controlling it? It first appeared on me about 5 years ago, and since then, every summer it flares up. The doctor gave me an antifungal shampoo to use on it but nothing I've tried seems to clear it up. I've tried Selsun shampoo and various other
Does anyone else have this condition or have any tips on controlling it? It first appeared on me about 5 years ago, and since then, every summer it flares up. The doctor gave me an antifungal shampoo to use on it but nothing I've tried seems to clear it up. I've tried Selsun shampoo and various other
helen_back
in
MY SKIN
11 years ago
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