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Pneumonia vaccination
Hi all. I have recently returned to Spain for the foreseeable future and managed to get my covid vaccination shortly after my arrival a few weeks ago. I had my flu vaccination in the UK just before we came out. I have to say that I have responded well to both vaccinations with no adverse side effects
Hi all. I have recently returned to Spain for the foreseeable future and managed to get my covid vaccination shortly after my arrival a few weeks ago. I had my flu vaccination in the UK just before we came out. I have to say that I have responded well to both vaccinations with no adverse side effects
Elispeth
in
PMRGCAuk
9 months ago
Tired Tavern - Discord server for people with CFS/ME and Long Covid
Hi guys, Just wanted to say that our CFS/ME and Long Covid Discord server has been up and running for two weeks now and we're close to 150 members. We're a very welcoming community that helps one another by sharing experiences, comfort and understanding. We also have server and community events coming
Hi guys, Just wanted to say that our CFS/ME and Long Covid Discord server has been up and running for two weeks now and we're close to 150 members. We're a very welcoming community that helps one another by sharing experiences, comfort and understanding. We also have server and community events coming
TiredTavern
in
Myalgic Encephalomyelitis Community
8 months ago
RA complicated by arthritis in knees
Morning, so I have increasing pain in knees, worse on left. Diagnosed with Degenerate Oesteo-Arthritis in both knees, treatment for which is steroid injection, for time being, but ultimately will need knee replacement surgery. My question is, does anyone have tips to reduce pain & swelling & preserve
Morning, so I have increasing pain in knees, worse on left. Diagnosed with Degenerate Oesteo-Arthritis in both knees, treatment for which is steroid injection, for time being, but ultimately will need knee replacement surgery. My question is, does anyone have tips to reduce pain & swelling & preserve
Mama-K
in
NRAS
8 months ago
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Shingles
I have CFS/ME, Fibromyalgia etcMy previous doctor from when I moved new what I had etc. I have had shingles maybe three times. But I can't understand why they have message my husband, who is younger then me and as diabetes for the first time for a shingles injections and he as never had shingles? Any
I have CFS/ME, Fibromyalgia etcMy previous doctor from when I moved new what I had etc. I have had shingles maybe three times. But I can't understand why they have message my husband, who is younger then me and as diabetes for the first time for a shingles injections and he as never had shingles? Any
sharron1
in
Fibromyalgia Action UK
9 months ago
Been a bit quiet, been a bit low. Repeating a week...
Hello all,So I've been fighting a cold/cough bug since the tail end of my hols last week. The last run I managed was on Monday of this week, so I'm feeling a bit disappointed in myself, but every intention of getting back to it today after work 🤞🏾 I've now decided it was "ok" to let my body rest,
Hello all,So I've been fighting a cold/cough bug since the tail end of my hols last week. The last run I managed was on Monday of this week, so I'm feeling a bit disappointed in myself, but every intention of getting back to it today after work 🤞🏾 I've now decided it was "ok" to let my body rest,
PuffingPanda
in
Couch to 5K
1 year ago
first time covid - symptoms expectation
Hello fellow RA warriors, I have been very careful since the start of the covid era - very limited outings/socializing, always mask up when out, no more gym exercise classes. I decided to enjoy the holiday a little bit more this year - dined out with a few family members in a crowded and popular restaurant
Hello fellow RA warriors, I have been very careful since the start of the covid era - very limited outings/socializing, always mask up when out, no more gym exercise classes. I decided to enjoy the holiday a little bit more this year - dined out with a few family members in a crowded and popular restaurant
Mymymy
in
NRAS
8 months ago
adrenals
please help , I am feeling really unwell ,dizzy , feel sick ,mentally very low,upset stomach,lost weight ,waking up after 4 hours sleep ,anxiety of the scale.from July till October tapered down from 6mg to 4.5 finished 28 October,stayed there to see how I was , I wasn’t feeling brilliant but I know I
please help , I am feeling really unwell ,dizzy , feel sick ,mentally very low,upset stomach,lost weight ,waking up after 4 hours sleep ,anxiety of the scale.from July till October tapered down from 6mg to 4.5 finished 28 October,stayed there to see how I was , I wasn’t feeling brilliant but I know I
Amilee
in
PMRGCAuk
9 months ago
Chillblains
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
GerryPL
in
CLL Support
9 months ago
Covid testing
Does anybody know if home carers are still expected to do Covid tests? I have a new carer and when she came today she was coughing a lot. I asked her when she had last tested and she said she hasn’t tested since January of this year.
Does anybody know if home carers are still expected to do Covid tests? I have a new carer and when she came today she was coughing a lot. I asked her when she had last tested and she said she hasn’t tested since January of this year.
thelmar
in
NRAS
8 months ago
Constant lower Back/Left Bum cheek pain
Hi All,I have adenomyosis and I have been having constant and chronic lower back pain and pain on my left bum cheek for 9 months. Does anyone else with adenomyosis have this problem? I've had a laparoscopy and endo wasn't found but I wouldn't be surprised if I have it too. It's tormenting me and hugely
Hi All,I have adenomyosis and I have been having constant and chronic lower back pain and pain on my left bum cheek for 9 months. Does anyone else with adenomyosis have this problem? I've had a laparoscopy and endo wasn't found but I wouldn't be surprised if I have it too. It's tormenting me and hugely
ABFr23
in
Endometriosis UK
8 months ago
filgotinib and shingles,
hi everyone Just getting over last 2 weeks of awful shingles ,my god painful or what!! As I am on filgotinib and it lists side effect can be reactivation of shingles virus,I can only assume it is that.Has anyone else had shingles while on any of the JAK meds? Pharmacist prescribed antivirals within
hi everyone Just getting over last 2 weeks of awful shingles ,my god painful or what!! As I am on filgotinib and it lists side effect can be reactivation of shingles virus,I can only assume it is that.Has anyone else had shingles while on any of the JAK meds? Pharmacist prescribed antivirals within
Doodlereggie
in
NRAS
4 months ago
Disability Allowance - Any Advice Please
Hi everybody. At a recent trip to hospital for my usual check ups a question was posed by one of the medical staff. “Are you getting Disability Allowance”? No I answered! “Well you should have a look at that” they replied “especially if you have had to stop work” So that got me thinking. I am 62, I
Hi everybody. At a recent trip to hospital for my usual check ups a question was posed by one of the medical staff. “Are you getting Disability Allowance”? No I answered! “Well you should have a look at that” they replied “especially if you have had to stop work” So that got me thinking. I am 62, I
Investigator1
in
Vasculitis UK
8 months ago
Foot/mouth hand or something else??
Does anyone know what this is. It started with red burning spots then turned into patches. Then I had chicken like pox all over my body and face. Hands rashes are similar to feet. But my thumbs are going white too and thin skin. Anyone know what's happening. I'm very stressed. Doctors are not helping
Does anyone know what this is. It started with red burning spots then turned into patches. Then I had chicken like pox all over my body and face. Hands rashes are similar to feet. But my thumbs are going white too and thin skin. Anyone know what's happening. I'm very stressed. Doctors are not helping
Shine54
in
LUPUS UK
9 months ago
Covid First Time
Well I have finally caught Covid, in fact it is the first time that I have noticeably caught anything since 2019. At the moment I have chills, vomiting and a headache=not happy. Just wondering if anyone has any tips or info. on how to stay as comfy as possible and anything to look out for Asthma wise
Well I have finally caught Covid, in fact it is the first time that I have noticeably caught anything since 2019. At the moment I have chills, vomiting and a headache=not happy. Just wondering if anyone has any tips or info. on how to stay as comfy as possible and anything to look out for Asthma wise
LittleZebra
in
Asthma Community Forum
8 months ago
Bam ibs
I have very problematic and symptomatic ibs and now i have severe bile acid malabsorption and i have arthritis msk i get pip for my msk and have just done a renewal for my pip i have put everything down about my bile acid malabsorption how it affects my daily life ,anyone on here gets pip for the bile
I have very problematic and symptomatic ibs and now i have severe bile acid malabsorption and i have arthritis msk i get pip for my msk and have just done a renewal for my pip i have put everything down about my bile acid malabsorption how it affects my daily life ,anyone on here gets pip for the bile
Netbet22
in
IBS Network
10 months ago
Covid and AF
Apologies if I posted this earlier. Despite countless jabs against covid (I am 79 ) and escaping the virus the past three and a half years I succumbed to the latest variant last Sunday 10th Dec. At first I thought it was just a heavy cold with a cough. Also I was thinking that I was more susceptible
Apologies if I posted this earlier. Despite countless jabs against covid (I am 79 ) and escaping the virus the past three and a half years I succumbed to the latest variant last Sunday 10th Dec. At first I thought it was just a heavy cold with a cough. Also I was thinking that I was more susceptible
Camelia23
in
AF Association
8 months ago
COVID
Doea anyone have any advice. I had my ablation in September and a nurse told me not to have a flu jab or covid booster. I am now stuck at home with Covid. I am a little worried about it triggering AFib.
Doea anyone have any advice. I had my ablation in September and a nurse told me not to have a flu jab or covid booster. I am now stuck at home with Covid. I am a little worried about it triggering AFib.
Be-still-my-heart
in
AF Association
8 months ago
Bands pulmonary fibrosis tomography
hello my story in short in 2022 I had covid 19 after recovery I did a lung X-ray which did not show anything suspicious now in September 2023 a year after covid19 I started having breathing difficulties I couldn't breathe deeply and I was falling into bed we can't I'm going to the end of the cascading
hello my story in short in 2022 I had covid 19 after recovery I did a lung X-ray which did not show anything suspicious now in September 2023 a year after covid19 I started having breathing difficulties I couldn't breathe deeply and I was falling into bed we can't I'm going to the end of the cascading
Petre84
in
Lung Conditions Community Forum
8 months ago
Phone-call from receptionist today
Only just joined and not sure where to begin as I feel as if I’m in shock a little and desperately trying to find out information. I had a phone call from the drs receptionist this afternoon to tell me I have hypothyroidism after some blood tests and needed to pick up a prescription which I would need
Only just joined and not sure where to begin as I feel as if I’m in shock a little and desperately trying to find out information. I had a phone call from the drs receptionist this afternoon to tell me I have hypothyroidism after some blood tests and needed to pick up a prescription which I would need
Benjipuss
in
Thyroid UK
8 months ago
covid meds and prednisolne
Evening all I have PMR and currently tapering Pred down, I am on 3 mg per day. However yesterday I tested positive for Covid. Two questions 1. do I need to inform my GP as my immune system is compromised the NHS site is not clear. 2. What meds does anyone suggest for the hacking cough, runny nose
Evening all I have PMR and currently tapering Pred down, I am on 3 mg per day. However yesterday I tested positive for Covid. Two questions 1. do I need to inform my GP as my immune system is compromised the NHS site is not clear. 2. What meds does anyone suggest for the hacking cough, runny nose
JAC1947
in
PMRGCAuk
8 months ago
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