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Covid Again
hi all just a quick question can Covid affected your lungs when you are on blood thinners?, I had Covid at the beginning of December which was pretty bad, i feel like I recovered well but I’m back to square one again my chest hurt and I’m a bit more breathless but I also suffer from severe anxiety and
hi all just a quick question can Covid affected your lungs when you are on blood thinners?, I had Covid at the beginning of December which was pretty bad, i feel like I recovered well but I’m back to square one again my chest hurt and I’m a bit more breathless but I also suffer from severe anxiety and
Cimmy
in
Lung Conditions Community Forum
7 months ago
Throat tightness
Hello has anyone had tightness in throat like pressure feeling? I can breathe and swallow ok but it's so annoying. I've been suffering severe fatigue and feeling like my body is full of led my GP continues to take blood and did mention I have hyperthyroidism before Christmas but didn't give me any
Hello has anyone had tightness in throat like pressure feeling? I can breathe and swallow ok but it's so annoying. I've been suffering severe fatigue and feeling like my body is full of led my GP continues to take blood and did mention I have hyperthyroidism before Christmas but didn't give me any
Joylene123
in
Thyroid UK
5 months ago
Christmas Covid
Looks like our Christmas present was Covid. At my partners mothers and both tested positive one this morning and the others last Thursday but so far I’m negative but sure I’ll get it. not sure where we picked it up as been careful. I’m not sure what to do meds wise as I took my 15mg of MTX yesterday
Looks like our Christmas present was Covid. At my partners mothers and both tested positive one this morning and the others last Thursday but so far I’m negative but sure I’ll get it. not sure where we picked it up as been careful. I’m not sure what to do meds wise as I took my 15mg of MTX yesterday
Alan7690
in
NRAS
7 months ago
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ACR (Microalbumin/Creatinine Ratio)
My Urine’s ACR result is 8.4 mg/mmol. HbA1C is 8.5. I am very worried. Kindly advise or provide insights.
My Urine’s ACR result is 8.4 mg/mmol. HbA1C is 8.5. I am very worried. Kindly advise or provide insights.
Limeandlemon
in
Diabetes India
5 months ago
My Christmas
I did not attend the family gathering unfortunately since I have anxiety inside indoor spaces with groups of people, and we have COVID and flu going around. My concern with COVID is that some people get long term symptoms like chronic fatigue, loss of smell or taste, and a few others. So it just still
I did not attend the family gathering unfortunately since I have anxiety inside indoor spaces with groups of people, and we have COVID and flu going around. My concern with COVID is that some people get long term symptoms like chronic fatigue, loss of smell or taste, and a few others. So it just still
davidthecoder
in
Anxiety and Depression Support
7 months ago
Covid update
I had a call back after 2.5 days from the covid medication delivery unit. They asked me to go to the local hospital to get an infusion of sotrovimab. The tablets form interacts with some of my medication so this one was chosen. I will let you know how I do on it.
I had a call back after 2.5 days from the covid medication delivery unit. They asked me to go to the local hospital to get an infusion of sotrovimab. The tablets form interacts with some of my medication so this one was chosen. I will let you know how I do on it.
artydutch
in
MPN Voice
7 months ago
cellulitis
I’ve been diagnosed today with cellulitis - never had it before and knew nothing about it so it’s all been a bit of a shock. I’ve been prescribed Flucloxacillin but unfortunately, by the time I was discharged from Urgent Care, the hospital pharmacy was closed so I can’t start them until the morning
I’ve been diagnosed today with cellulitis - never had it before and knew nothing about it so it’s all been a bit of a shock. I’ve been prescribed Flucloxacillin but unfortunately, by the time I was discharged from Urgent Care, the hospital pharmacy was closed so I can’t start them until the morning
Janann25
in
PMRGCAuk
6 months ago
Periods delayed after steroid injections
Hi,Has anyone had the experience of their periods being delayed after having steroid injections. If so, for how long? I'm a week late. They haven't been this late in a long while. I have an IVF consultation next month so I'm worried they won't return Thanks
Hi,Has anyone had the experience of their periods being delayed after having steroid injections. If so, for how long? I'm a week late. They haven't been this late in a long while. I have an IVF consultation next month so I'm worried they won't return Thanks
ABFr23
in
NRAS
7 months ago
Neupro Patch
I saw a consultant in the UK a month or so ago and explained that my transition from Mirapexin to Pregabalin was not going well. At that time, I was taking 150mg Pregabalin and 4 x 0.088 Mirapexin and that at that level i was getting some relief but that any reduction from that in the Mirapexin left
I saw a consultant in the UK a month or so ago and explained that my transition from Mirapexin to Pregabalin was not going well. At that time, I was taking 150mg Pregabalin and 4 x 0.088 Mirapexin and that at that level i was getting some relief but that any reduction from that in the Mirapexin left
Ced60
in
Restless Legs Syndrome
1 year ago
Pain management Team
I have been waiting for 4 years to see someone in the pain management clinic at our local hospital. What a complete joke. When are the doctors and so called specialists going to help a patient who is in considerable pain and saying to him I want to cut my foot off. He was a complete waste of time, why
I have been waiting for 4 years to see someone in the pain management clinic at our local hospital. What a complete joke. When are the doctors and so called specialists going to help a patient who is in considerable pain and saying to him I want to cut my foot off. He was a complete waste of time, why
Imagine1
in
Pain Concern
7 months ago
What causes cold sweats?
I’ve been taking Prednisolone for PMR since May 2021. I’ve been very gradually reducing and have been on 4mg for 1 month. I take the Pred at about 5am with yoghourt and banana. I had Covid 2 weeks ago. I didn’t up the Pred dose. I have no PMR pain. I feel ok in the mornings but have high anxiety
I’ve been taking Prednisolone for PMR since May 2021. I’ve been very gradually reducing and have been on 4mg for 1 month. I take the Pred at about 5am with yoghourt and banana. I had Covid 2 weeks ago. I didn’t up the Pred dose. I have no PMR pain. I feel ok in the mornings but have high anxiety
Geology
in
PMRGCAuk
1 day ago
Feeling cold all the time
Hi, I have scleroderma and reynauds and while I am used to having cold hands and feet of late I am very cold all over, even my core. I was wondering if I might be low on some vitamins or minerals and was hoping someone might be able to advise. Regards, Darren
Hi, I have scleroderma and reynauds and while I am used to having cold hands and feet of late I am very cold all over, even my core. I was wondering if I might be low on some vitamins or minerals and was hoping someone might be able to advise. Regards, Darren
Deiseboy
in
Scleroderma & Raynaud's UK (SRUK)
2 days ago
10 year old with red patches on her face
Hi all,Just tying to figure out what we're dealing with here using your experience. My daughter, which is 10, started what looks to be a case of impetigo (meaning blisters in her nostril, crust and typical looking scabs). She only had few spots (under her nose and in top of one nostril). We started
Hi all,Just tying to figure out what we're dealing with here using your experience. My daughter, which is 10, started what looks to be a case of impetigo (meaning blisters in her nostril, crust and typical looking scabs). She only had few spots (under her nose and in top of one nostril). We started
euxy103
in
LUPUS UK
2 days ago
PV and common Cold
Morning all, Only diagnosed with PV since Nov 23. Low risk as im 38 and platelets have stopped increasing since the introduction of aspirin and a few other for the itch. In the last 2 months it feels like im constantly battling a cold. I get slight relief for a few days and then its back. Anyone else
Morning all, Only diagnosed with PV since Nov 23. Low risk as im 38 and platelets have stopped increasing since the introduction of aspirin and a few other for the itch. In the last 2 months it feels like im constantly battling a cold. I get slight relief for a few days and then its back. Anyone else
Headaball
in
MPN Voice
4 days ago
hand and foot scan question
I have a letter telling me to stop taking pain medication for four weeks Before my hand and foot scan. Im taking liquid naproxen as it takes the edge off, however I’m unable to even manage a day with out pain relief Have you had a hand foot scan and told not to take and meds for four weeks till
I have a letter telling me to stop taking pain medication for four weeks Before my hand and foot scan. Im taking liquid naproxen as it takes the edge off, however I’m unable to even manage a day with out pain relief Have you had a hand foot scan and told not to take and meds for four weeks till
Beachwalk
in
NRAS
4 days ago
Is pseudamonas contagious??
Hi, Does anyone know if my pseudamonas could be transmitted to those who live in close proximity? I always thought not but I've been worried about my OH's persistent cough - I know there could be many other reasons for his cough and his recent sputum test was clear but....
Hi, Does anyone know if my pseudamonas could be transmitted to those who live in close proximity? I always thought not but I've been worried about my OH's persistent cough - I know there could be many other reasons for his cough and his recent sputum test was clear but....
Leafsweeper
in
Lung Conditions Community Forum
5 days ago
freezyfeet
Nothing seems to help with cold feet except my heated mat and gloves for my hands.
Nothing seems to help with cold feet except my heated mat and gloves for my hands.
Freezyfeet
in
Scleroderma & Raynaud's UK (SRUK)
6 days ago
UK winter flu vaccines, booking available
Boots are now taking bookings for the UK winter flu vaccines.
Boots are now taking bookings for the UK winter flu vaccines.
fapumpkin
in
CLL Support
7 days ago
Covid
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
JLAR01
in
LUPUS UK
7 months ago
Blood in urine/uti symptoms but no infection
I'm currently in a flare up, following a hysterectomy nearly 5 months ago for Fibroids and Adenomyosis. They now think I have Occult endometriosis, as my pelvic pain has flared up again since starting hrt. Ive been referred to a bsge centre.My bladder symptoms are awful I feel like I have a raging uti
I'm currently in a flare up, following a hysterectomy nearly 5 months ago for Fibroids and Adenomyosis. They now think I have Occult endometriosis, as my pelvic pain has flared up again since starting hrt. Ive been referred to a bsge centre.My bladder symptoms are awful I feel like I have a raging uti
Mindfullness4791
in
Endometriosis UK
8 days ago
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