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Anyone had hand therapy for Chronic repetitive strain injury of the wrists?
My question is has anyone ever had hand therapy for chronic tendonitis or like a chronic repetitive strain injury in your wrist? And if so did it help with the pain? This is the only thing that I've not tried besides obviously I've not tried surgery and I asked my orthopedic hand dr about it and he doesn't
My question is has anyone ever had hand therapy for chronic tendonitis or like a chronic repetitive strain injury in your wrist? And if so did it help with the pain? This is the only thing that I've not tried besides obviously I've not tried surgery and I asked my orthopedic hand dr about it and he doesn't
Hidden
in
Pain Concern
9 months ago
enlarged lymp node
I had a ct scan yesterday and got the results today. I have enlarged left axillary lymph nodes, largest measuring 19x14 mm, previously subcentimeter and measured 10x8.5. Enlarged left subpectoral lymph nodes are identified. Nothing on the right side. I had a covid vacine about 2-3 weeks ago. The
I had a ct scan yesterday and got the results today. I have enlarged left axillary lymph nodes, largest measuring 19x14 mm, previously subcentimeter and measured 10x8.5. Enlarged left subpectoral lymph nodes are identified. Nothing on the right side. I had a covid vacine about 2-3 weeks ago. The
DianeSH
in
CLL Support
8 months ago
Covid
Hello, everyone I have severe emphysema and I did a test yesterday and I got covid š± I am scared it gonna attack my lungs, my chest feeling tighter.Anyone else had covid with emphysema, how did you take care of yourself to stop it going to the lungs.
Hello, everyone I have severe emphysema and I did a test yesterday and I got covid š± I am scared it gonna attack my lungs, my chest feeling tighter.Anyone else had covid with emphysema, how did you take care of yourself to stop it going to the lungs.
Madonna1
in
COPD Friends
8 months ago
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Pituitary gland not producing TSH
Oct 14, 2022 I had a 3rd Covid Booster shot. The next day I had the "normal" flu symptoms. Oct 20, six days later, I felt I had been hit by a bus, hurting literally from head to toe with different kinds of pain along with heartburn and leg swelling. I figured this was just a reaction that would subside
Oct 14, 2022 I had a 3rd Covid Booster shot. The next day I had the "normal" flu symptoms. Oct 20, six days later, I felt I had been hit by a bus, hurting literally from head to toe with different kinds of pain along with heartburn and leg swelling. I figured this was just a reaction that would subside
Cricket-mas
in
Thyroid UK
8 months ago
drugs repurposing: another promising path!
not yet tested for prostate cancer (I think) but stillā¦ āBut two years after starting a treatment regimen that combined ruxolitinib with the checkpoint inhibitor nivolumabāa current standard of careā87% of patients were still alive, and 46% stopped exhibiting signs of cancer progression altogether.ā
not yet tested for prostate cancer (I think) but stillā¦ āBut two years after starting a treatment regimen that combined ruxolitinib with the checkpoint inhibitor nivolumabāa current standard of careā87% of patients were still alive, and 46% stopped exhibiting signs of cancer progression altogether.ā
Maxone73
in
Advanced Prostate Cancer
26 days ago
Advice on increasing Pred for breathlessness and persistent cough
My GP told me that breathlessness is a symptom of PMR, so I can't seek her advice on how to manage this cough etc. Some people are saying that Eris Covid is around and it presents as a bad cough which does not show up as positive on home covid testing kits. I have had a persistent productive cough
My GP told me that breathlessness is a symptom of PMR, so I can't seek her advice on how to manage this cough etc. Some people are saying that Eris Covid is around and it presents as a bad cough which does not show up as positive on home covid testing kits. I have had a persistent productive cough
Motida
in
PMRGCAuk
11 months ago
Exercise and PMR
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
Indigo2417
in
PMRGCAuk
8 months ago
Advice please...
My fibro always gets worse in cold weather so bath soaks are my best friends at the moment, however, my boiler and heating stopped working few days ago, I called my housing association and they fixed the heaters, but for hot water I was told its not considered emergency as you can boil kettles of water
My fibro always gets worse in cold weather so bath soaks are my best friends at the moment, however, my boiler and heating stopped working few days ago, I called my housing association and they fixed the heaters, but for hot water I was told its not considered emergency as you can boil kettles of water
YMEPLEASE
in
Fibromyalgia Action UK
5 months ago
Being taking off Pegasys. :( Looking for alternatives
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
Hi all, I have ET & PV with Jak2. I am 40. I have been on aspirin for over 10 years, but had to start Pegasys 3 months ago. I haven't tolerated it well. Severe shortness of breath etc. My hematologist reduced my dose to 30 per week, but I am suffering with hypertension (150 to 69/96 on average) and
JustKeepSw1mming
in
MPN Voice
10 months ago
Anyone find cold plunge or sauna helpful?
I'm six weeks in on ADT. Working to stay ahead of fatigue with resistance training and weighted vest walking as I gear up for radiation and chemo in the next few months. Anyone done any cold plunge or sauna to help battle side effects or get better sleep? What was your experience?
I'm six weeks in on ADT. Working to stay ahead of fatigue with resistance training and weighted vest walking as I gear up for radiation and chemo in the next few months. Anyone done any cold plunge or sauna to help battle side effects or get better sleep? What was your experience?
PuraVida2024
in
Advanced Prostate Cancer
1 month ago
QoL-Lick the spoon
This is an IF, WHEN and NOW thought process. I know many of you have already been through this stage because of your cancer but a few people ( new members and a few regulars) havenāt embraced these ideas. How many of you have probably said to yourself IF this treatment works weāre going to go on a
This is an IF, WHEN and NOW thought process. I know many of you have already been through this stage because of your cancer but a few people ( new members and a few regulars) havenāt embraced these ideas. How many of you have probably said to yourself IF this treatment works weāre going to go on a
MouseAddams
in
Advanced Prostate Cancer
8 months ago
Covid & dosing
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
amala57
in
Thyroid UK
8 months ago
Have COVID - should I get Paxlovid/
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
Lambo1
in
CLL Support
8 months ago
Prescribed Naproxine 250 twice a day for hip bursitis is that dangerous with Pred
I was prescribed Naproxine 250 twice a day yesterday for bursitis ? on right hip. Pain is so bad dr. gave a steroid injection. Suggested I take up to 4g of Paracetamol if necessary. Just read of NHS site that Naproxine and Pred are not compatible. Is this true for short time use? If so what
I was prescribed Naproxine 250 twice a day yesterday for bursitis ? on right hip. Pain is so bad dr. gave a steroid injection. Suggested I take up to 4g of Paracetamol if necessary. Just read of NHS site that Naproxine and Pred are not compatible. Is this true for short time use? If so what
Motida
in
PMRGCAuk
9 months ago
LORIS AI predicts patient outcomes with immune checkpoint blockade therapy
Sort of important because immune checkpoint blockade therapy apparently has a lower success rate that bat bipolar androgen therapy. LORIS robustly predicts patient outcomes with immune checkpoint blockade therapy using common clinical, pathologic and genomic features | Nature Cancer Https://www.nature.com
Sort of important because immune checkpoint blockade therapy apparently has a lower success rate that bat bipolar androgen therapy. LORIS robustly predicts patient outcomes with immune checkpoint blockade therapy using common clinical, pathologic and genomic features | Nature Cancer Https://www.nature.com
cesanon
in
Advanced Prostate Cancer
1 month ago
Natural cycle FET likely to be cancelled due to ovulation on small follicle. What does this mean about my eggs/ ovaries? Having a wobble
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Minniemouse88
in
Fertility Network UK
8 months ago
Covid, strange beast.
I find Covid a bizarre virus. I have had 3 times , hospitalised once. I am in remission after stage 4 diagnosis in 2020. My wife last returned from a company business meeting in Malta attended by 500 employees. She and many of her work mates now in bed with Covid. This is the 4th time my wife has had
I find Covid a bizarre virus. I have had 3 times , hospitalised once. I am in remission after stage 4 diagnosis in 2020. My wife last returned from a company business meeting in Malta attended by 500 employees. She and many of her work mates now in bed with Covid. This is the 4th time my wife has had
stevesmith1964
in
CLL Support
8 months ago
Fod Map Diet
Good morning have been on Fodmap diet since March . Has been getting less strict as I eat some dairy but my diet is generally getting more and more restricted.Im also a Pescatarian and feel that I arenāt getting enough protein or variation . Main Symptoms are Anxiety,dizziness,tinnitus,Nausea,wind
Good morning have been on Fodmap diet since March . Has been getting less strict as I eat some dairy but my diet is generally getting more and more restricted.Im also a Pescatarian and feel that I arenāt getting enough protein or variation . Main Symptoms are Anxiety,dizziness,tinnitus,Nausea,wind
Imisspizza
in
IBS Network
8 months ago
Shingles
Hi all, My friend has Shingles. With PMR is it advisable to stay away until after breakout. Reading conflicting advice. Much appreciated yet again!! Thank you.
Hi all, My friend has Shingles. With PMR is it advisable to stay away until after breakout. Reading conflicting advice. Much appreciated yet again!! Thank you.
Fredddie
in
PMRGCAuk
1 year ago
Afib worse since Ablation
I had Covid in Oct 2022. I was 57 at the time and in really great shape. I exercise everyday, average about 15,000 steps a day and fast 2 to 3 days a week. As my Covid was winding down and I was feeling better I started having Afib Episodes for the first time in my life. They started off
I had Covid in Oct 2022. I was 57 at the time and in really great shape. I exercise everyday, average about 15,000 steps a day and fast 2 to 3 days a week. As my Covid was winding down and I was feeling better I started having Afib Episodes for the first time in my life. They started off
filmguy5
in
AF Association
9 months ago
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