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Covid jab and pausing methotrexate
Hello, please can anyone help with a covid jab/methotrexate question... I have problems with my memory but I am fairly sure there were posts about a published report saying Methotrexate could stop the jab taking effect, and to stop taking it for 2 weeks ... but am I misremembering, and if not was
Hello, please can anyone help with a covid jab/methotrexate question... I have problems with my memory but I am fairly sure there were posts about a published report saying Methotrexate could stop the jab taking effect, and to stop taking it for 2 weeks ... but am I misremembering, and if not was
Ann1A
in
PMRGCAuk
9 months ago
Dizziness / Vertigo whilst on Pred
I’ve been suffering with nausea and dizziness whilst on Pred, whilst this has been awful it’s not as bad as the PMR pain I was experiencing. My GP and an a nurse have suggested this could be to do with the inner ear. I do suffer from travel sickness and avoid roller coasters / waltzers because they
I’ve been suffering with nausea and dizziness whilst on Pred, whilst this has been awful it’s not as bad as the PMR pain I was experiencing. My GP and an a nurse have suggested this could be to do with the inner ear. I do suffer from travel sickness and avoid roller coasters / waltzers because they
SpaghettiWestern99
in
PMRGCAuk
8 months ago
Thrush?
Hi has anyone had thrush so bad that your swollen, got sores around the entrance to your vagina, been itchy and when you pee it hurts so bad you wanna cry? I'm using caneston external cream and the applied the internal one yesterday but it doesn't seem to be getting any better. Doctors are all closed
Hi has anyone had thrush so bad that your swollen, got sores around the entrance to your vagina, been itchy and when you pee it hurts so bad you wanna cry? I'm using caneston external cream and the applied the internal one yesterday but it doesn't seem to be getting any better. Doctors are all closed
Kayloufell
in
BASHH
5 months ago
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Testosterone
Hi everyone, I'm a long time ThyroidUK participant. Right now the thyroid replacement is good, vitamins, minerals, are all great. I'm very particular to ensure this. I use HRT (Triestrogen/progesterone) topical cream and have used since age 45 and I'm now 65. Here's the problem: in March
Hi everyone, I'm a long time ThyroidUK participant. Right now the thyroid replacement is good, vitamins, minerals, are all great. I'm very particular to ensure this. I use HRT (Triestrogen/progesterone) topical cream and have used since age 45 and I'm now 65. Here's the problem: in March
gabkad
in
Menopause and Perimenopause Support
9 months ago
RA and (periodontitis)gum disease 😱
morning all! So yesterday I went to the dentist because a large filling on a back tooth that I’ve had for many years fell out!when I got there the dentist popped a temporary one in and he did some X-rays he then said I have periodontitis gum disease 😱with bone loss he said to start with I need to have
morning all! So yesterday I went to the dentist because a large filling on a back tooth that I’ve had for many years fell out!when I got there the dentist popped a temporary one in and he did some X-rays he then said I have periodontitis gum disease 😱with bone loss he said to start with I need to have
Mybirthday1975
in
NRAS
4 months ago
Overactive Bladder Syndrome
Bit strange to post this here but bear with me please. It seems that many of the med's for OAB have a side effect of high heart rate. I've been diagnosed with Paroxysmal Tachycardia and am trying Tolterodine for my OAB (which increased my comfort level considerably) but have had to stop as my monthly
Bit strange to post this here but bear with me please. It seems that many of the med's for OAB have a side effect of high heart rate. I've been diagnosed with Paroxysmal Tachycardia and am trying Tolterodine for my OAB (which increased my comfort level considerably) but have had to stop as my monthly
Oggy99
in
AF Association
8 months ago
Covid an d Pmr
Hi everyone, I have PMR an d have been testing positive for eleven days for Covid. Am currently on twelve an d a half mg of Pred a day.I have Kyphoscoliosis which is a Spinal Deformity which causes my lung space to be a bit compromised so am worried because have got th e most awful cough which is making
Hi everyone, I have PMR an d have been testing positive for eleven days for Covid. Am currently on twelve an d a half mg of Pred a day.I have Kyphoscoliosis which is a Spinal Deformity which causes my lung space to be a bit compromised so am worried because have got th e most awful cough which is making
Attic
in
PMRGCAuk
9 months ago
Shingles vaccination - or not?
Hi all, hope to get some helpful advice on subject of shingles vaccination. Shingrix is available in my country (Norway) so I enquired of my GP about any recommendation in the light of my long-term polymyalgia (7+ years, maintained on 2.5 mg daily pred for about a year but unbelievably resistant to even
Hi all, hope to get some helpful advice on subject of shingles vaccination. Shingrix is available in my country (Norway) so I enquired of my GP about any recommendation in the light of my long-term polymyalgia (7+ years, maintained on 2.5 mg daily pred for about a year but unbelievably resistant to even
11541stella
in
PMRGCAuk
8 months ago
Otomize ear spray
HiI have an outer ear infection in both ears and I've been prescribed Otomize ear spray but it's making me feel really sick when I use it, has anyone else had this experience? I don't know if it's helping my tinnitus as I only started taking it yesterday afternoon. I'm currently using a hot water bottle
HiI have an outer ear infection in both ears and I've been prescribed Otomize ear spray but it's making me feel really sick when I use it, has anyone else had this experience? I don't know if it's helping my tinnitus as I only started taking it yesterday afternoon. I'm currently using a hot water bottle
Coxy00
in
Tinnitus UK
8 months ago
update on rls treatment
Gp has put me on 20mg Norspan patches and I am having acupunture and reflexology as well. Shumbah has suggested applying the sesame oil on troublesome leg....I have started that and will keep you informed....I have only been doing it for a week, but I think it is having some effect. The tugging, pulling
Gp has put me on 20mg Norspan patches and I am having acupunture and reflexology as well. Shumbah has suggested applying the sesame oil on troublesome leg....I have started that and will keep you informed....I have only been doing it for a week, but I think it is having some effect. The tugging, pulling
Hidden
in
Restless Legs Syndrome
8 months ago
My story
Hi, it all started by going into hospital for day surgery for Hemorrhoids. Within 36 hours my wife had taken me back to A & E with a high heart rate and low blood pressure. I was also in a lot of pain, which I put down to the surgery for Hemorrhoids. I was soon in majors and within a few hours I was
Hi, it all started by going into hospital for day surgery for Hemorrhoids. Within 36 hours my wife had taken me back to A & E with a high heart rate and low blood pressure. I was also in a lot of pain, which I put down to the surgery for Hemorrhoids. I was soon in majors and within a few hours I was
Hikingman
in
ICUsteps
8 months ago
Greater use of Benlysta, Saphnelo seen in US, EU to treat lupus
Goal to reduce long-term glucocorticoids use to prevent side effects
In both the U.S. and Europe, clinicians want to limit treatment with glucocorticoids — steroid hormones whose long-term use for autoimmune diseases is tied to serious side effects — among people with moderate to severe lupus
Goal to reduce long-term glucocorticoids use to prevent side effects
In both the U.S. and Europe, clinicians want to limit treatment with glucocorticoids — steroid hormones whose long-term use for autoimmune diseases is tied to serious side effects — among people with moderate to severe lupus
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
8 months ago
Flu and Covid vaccine
I was diagnosed with lupus in March this year. I dont know if I should take the flu and covid vaccine. I am scared it will make my lupus worse. Has anyone here take the vaccine?
I was diagnosed with lupus in March this year. I dont know if I should take the flu and covid vaccine. I am scared it will make my lupus worse. Has anyone here take the vaccine?
kali9
in
LUPUS UK
7 months ago
Acalabrutinib/COVID/swollen lymph nodes under arm
Hi, I’ve been on Acalabrutinib for almost a year now. I have SLL. Everything had been going wonderfully, my lymph nodes significantly decreased in size, my 3-months follow up scan showed great results, my blood work looked normal, and the side effects were minimal. I recently noticed, however, that
Hi, I’ve been on Acalabrutinib for almost a year now. I have SLL. Everything had been going wonderfully, my lymph nodes significantly decreased in size, my 3-months follow up scan showed great results, my blood work looked normal, and the side effects were minimal. I recently noticed, however, that
Tofa80
in
CLL Support
9 months ago
Heart problems and the Covid autumn booster
Just had an interesting thought I'm below the 65 age limit for the covid autumn booster but I automatically get the flu jab each year as I have other problems. After having a heart attack last year would this qualify me for the autumn booster or not I had it last autumn but the goal post for age has
Just had an interesting thought I'm below the 65 age limit for the covid autumn booster but I automatically get the flu jab each year as I have other problems. After having a heart attack last year would this qualify me for the autumn booster or not I had it last autumn but the goal post for age has
Coopergirl52
in
British Heart Foundation
9 months ago
If it’s not one thing, it's another! Update
Following on from the previous post, I had my appointment with the Ophthalmology Surgical Unit yesterday. Basically appeared to be a couple of pre-op tests to take measurements of my eyes. I’ve been given a contact number to call in a day or two to find out where on the waiting list I am. Hopefully
Following on from the previous post, I had my appointment with the Ophthalmology Surgical Unit yesterday. Basically appeared to be a couple of pre-op tests to take measurements of my eyes. I’ve been given a contact number to call in a day or two to find out where on the waiting list I am. Hopefully
Gulfstream_Maggie
in
Fibromyalgia Action UK
9 months ago
Cold virus
I’ve had PMR for two years now and on 8mg pred attempting my second tapering cycle. I’ve have a really heavy cold now for over a week which started as a mild cold for two weeks before that. I’m wondering if my immune system is reducing my ability to get on top of this and allowing it to prevail much
I’ve had PMR for two years now and on 8mg pred attempting my second tapering cycle. I’ve have a really heavy cold now for over a week which started as a mild cold for two weeks before that. I’m wondering if my immune system is reducing my ability to get on top of this and allowing it to prevail much
Mervetheswerve
in
PMRGCAuk
6 months ago
overlapping symptoms
hi all I’ve finally seen a rheumatologist and he wasn’t able to give me a diagnosis as he says I don’t present the classic symptoms for any one particular autoimmune disease but I have overlapping symptoms of more than one condition. The hair loss and rash seem to be puzzling them too. I’ve been prescribed
hi all I’ve finally seen a rheumatologist and he wasn’t able to give me a diagnosis as he says I don’t present the classic symptoms for any one particular autoimmune disease but I have overlapping symptoms of more than one condition. The hair loss and rash seem to be puzzling them too. I’ve been prescribed
TheRedOnes
in
LUPUS UK
6 months ago
Mum grew her angel wings
hi all, I just wanted to write a post on here as I sadly lost my mum last week after a 7 year battle with PSP. Although it was pneumonia that took her in the end. I just wanted to write on here to say, give your loved ones suffering an extra big hug this Christmas and remember to be their loved one
hi all, I just wanted to write a post on here as I sadly lost my mum last week after a 7 year battle with PSP. Although it was pneumonia that took her in the end. I just wanted to write on here to say, give your loved ones suffering an extra big hug this Christmas and remember to be their loved one
Janice52
in
PSP Association
6 months ago
Flare up after ear infection
I've had ear infection which the doctor gave me antibiotic spray for, thankfully ear pain had gone after a few days, but left with jaw pain, headaches and extreme exhaustion, as soon as I feel a little better I feel I have the energy to do a little bit, then I'm straight down again after the slightest
I've had ear infection which the doctor gave me antibiotic spray for, thankfully ear pain had gone after a few days, but left with jaw pain, headaches and extreme exhaustion, as soon as I feel a little better I feel I have the energy to do a little bit, then I'm straight down again after the slightest
Bue2
in
Fibromyalgia Action UK
8 months ago
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