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still not diagnosed but concerned about IBS
Sorry for lengthy post I am new here. I started an antibiotics course (one week) Doxycycline on 24 April 2023 for throat infection and fever,as soon I finish it, I started having diarrhoea. That time I was in very stress and depression for another reason. It's been almost over 9 months now. Diarrhea
Sorry for lengthy post I am new here. I started an antibiotics course (one week) Doxycycline on 24 April 2023 for throat infection and fever,as soon I finish it, I started having diarrhoea. That time I was in very stress and depression for another reason. It's been almost over 9 months now. Diarrhea
Fmkhan
in
IBS Network
10 months ago
Laryngitis and lupus
Hi, I am having my 2nd bout of laryngitis in 10 weeks, having never having had it before. I have just looked on Doctor Google and it says that my laryngitis can be caused by my lupus. Is this correct? Is this something I need to mention to my lupus specialist? I am due to start on methotrexate next
Hi, I am having my 2nd bout of laryngitis in 10 weeks, having never having had it before. I have just looked on Doctor Google and it says that my laryngitis can be caused by my lupus. Is this correct? Is this something I need to mention to my lupus specialist? I am due to start on methotrexate next
pattypatchwork
in
LUPUS UK
5 months ago
Anti viral?
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Does anyone know if they're still giving anti viral medication for a positive covid patient? I'm on rituximab and azathioprine aswell as prednisolone. I've not yet done a test but have been feeling breathless and coughing more than normal. I'm not allowed to have my covid or flu vaccinations due to
Vqueen
in
Vasculitis UK
8 months ago
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Apixaban
Hello, I had multiple blood clots in both lungs, pneumonia and also found multiple nodules both lungs sized 5mm and 6mm. This was August 23. I was on apixaban which they stopped on 12th. On 14th I started my period but haven't stopped. It keeps going to black blood then back to red .My hands are cold
Hello, I had multiple blood clots in both lungs, pneumonia and also found multiple nodules both lungs sized 5mm and 6mm. This was August 23. I was on apixaban which they stopped on 12th. On 14th I started my period but haven't stopped. It keeps going to black blood then back to red .My hands are cold
Abbielee
in
Lung Conditions Community Forum
5 months ago
First Post - Inhaler side effects worth it?
I hope this message finds you all well. I'm new to this forum and eager to connect with others who may have experience or insights into managing asthma. Allow me to introduce myself. I recently received some concerning news from my healthcare provider regarding my respiratory health. Despite having
I hope this message finds you all well. I'm new to this forum and eager to connect with others who may have experience or insights into managing asthma. Allow me to introduce myself. I recently received some concerning news from my healthcare provider regarding my respiratory health. Despite having
Damacian
in
Asthma Community Forum
5 months ago
Help! Stomach Bug & Holiday!
For over a week I have had some sort of stomach bug with awful pains in the lower stomach, causing loose stools, feeling chilled then hot, with a recurring headache. I contacted my doctor asking for urgent stool tests, as I am due to go on holiday to Spain next Monday, just in case it is a stomach bug
For over a week I have had some sort of stomach bug with awful pains in the lower stomach, causing loose stools, feeling chilled then hot, with a recurring headache. I contacted my doctor asking for urgent stool tests, as I am due to go on holiday to Spain next Monday, just in case it is a stomach bug
laurajn087
in
IBS Network
10 months ago
walking aids???
has any used a walking aid to improve balance as I walk looking at the ground and I can’t look to the side without stopping first .. flat ground is the best and uneven or incline causes pain in my old hamstring injury and the new hip pain I have developed .. I also still walk slightly to one side
has any used a walking aid to improve balance as I walk looking at the ground and I can’t look to the side without stopping first .. flat ground is the best and uneven or incline causes pain in my old hamstring injury and the new hip pain I have developed .. I also still walk slightly to one side
Teazymaid
in
Headway
11 days ago
B12 Ampoules
Hello everyone. I hope you are all keeping well 🙏 I am slowly recovering from Covid which I caught 6 weeks ago. I had the booster vaccine- the 4th vaccine-It takes 2 weeks to become effective and I managed to catch Covid before the vaccine kicked in. Just my luck ! 🙄Wish I could be so lucky with
Hello everyone. I hope you are all keeping well 🙏 I am slowly recovering from Covid which I caught 6 weeks ago. I had the booster vaccine- the 4th vaccine-It takes 2 weeks to become effective and I managed to catch Covid before the vaccine kicked in. Just my luck ! 🙄Wish I could be so lucky with
dollcat
in
Pernicious Anaemia Society
8 months ago
What would cause spontaneous prostate stimulation?
What would cause spontaneous prostate stimulation while lying on my back? When I lie down, in a few seconds it feels like someone is manually stimulating my prostate. This lasts for hours at a time and I cannot sleep. This started immediately after a nocturnal emission, and I haven't had one since, even
What would cause spontaneous prostate stimulation while lying on my back? When I lie down, in a few seconds it feels like someone is manually stimulating my prostate. This lasts for hours at a time and I cannot sleep. This started immediately after a nocturnal emission, and I haven't had one since, even
Hidden
in
Men's Health Forum
17 days ago
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
Free Genetic Testing Promise Trial
When I was diagnosed with this cancer and looked into this forum for guidance the topic of genetic testing and its potential applications sounded like something I should investigate since I had no info on my biological father’s medical history and my mom died of cervical cancer. My local urologist wanted
When I was diagnosed with this cancer and looked into this forum for guidance the topic of genetic testing and its potential applications sounded like something I should investigate since I had no info on my biological father’s medical history and my mom died of cervical cancer. My local urologist wanted
Mgtd
in
Advanced Prostate Cancer
18 days ago
Habituation
Hi. I'm 14 months in with T. Aged 47, male. Has several hearing checks, minor hearing loss but doesn't warrant hearing aids. My main question was about habituation. How exactly do you define this? I've got to a point were it doesn't cause me distress, it's more annoying than anything else. Is this a
Hi. I'm 14 months in with T. Aged 47, male. Has several hearing checks, minor hearing loss but doesn't warrant hearing aids. My main question was about habituation. How exactly do you define this? I've got to a point were it doesn't cause me distress, it's more annoying than anything else. Is this a
Zicaton
in
Tinnitus UK
20 days 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 😱 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 😱 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
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
Finished Venetoclax, then Covid
My doctor prescribed Venetoclax after two rounds of chemo/immuno infusions to fight CLL. I felt great! Swimming half a mile, felt strong. Then bronchitis, pneumonia, and Covid. Was hospitalized and released in 6 days. But my home convalescence is not what I expected. Weakness, coughing, general severe
My doctor prescribed Venetoclax after two rounds of chemo/immuno infusions to fight CLL. I felt great! Swimming half a mile, felt strong. Then bronchitis, pneumonia, and Covid. Was hospitalized and released in 6 days. But my home convalescence is not what I expected. Weakness, coughing, general severe
Healmenow
in
CLL Support
7 months ago
drugs repurposing: another promising path!
not yet tested for prostate cancer (I think) but still… “But two years after starting a treatment regimen that combined ruxolitinib with the checkpoint inhibitor nivolumab—a current standard of care—87% of patients were still alive, and 46% stopped exhibiting signs of cancer progression altogether.”
not yet tested for prostate cancer (I think) but still… “But two years after starting a treatment regimen that combined ruxolitinib with the checkpoint inhibitor nivolumab—a current standard of care—87% of patients were still alive, and 46% stopped exhibiting signs of cancer progression altogether.”
Maxone73
in
Advanced Prostate Cancer
26 days 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
Cold hands
I have conventional Raynaud's disease but I have notic ed when I play table tennis or do other things with my hands they remain cold even though the rest of my body is very warm. Also, I wear 250 denier tights and although my feet feel sort of warm, when I take my tights off they are freezing cold.
I have conventional Raynaud's disease but I have notic ed when I play table tennis or do other things with my hands they remain cold even though the rest of my body is very warm. Also, I wear 250 denier tights and although my feet feel sort of warm, when I take my tights off they are freezing cold.
AustenLover
in
Scleroderma & Raynaud's UK (SRUK)
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
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