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post Covid setback
Does anyone have experience with b12d recovery setbacks after Covid? I am 2 months into weekly injections, and had really started so see improvements. Then Covid struck. I am 18 days post-positive test…and my leg tremors have become far more noticeable, along with a resurgence of nerve pains in my hands
Does anyone have experience with b12d recovery setbacks after Covid? I am 2 months into weekly injections, and had really started so see improvements. Then Covid struck. I am 18 days post-positive test…and my leg tremors have become far more noticeable, along with a resurgence of nerve pains in my hands
MuppDog
in
Pernicious Anaemia Society
8 months ago
Rotten Head cold
I have developed overnight the most rotten head cold .. Headache is really bad ..I know inside is all inflamed I can feel it ...eyes are running along with my nose ... We close the business on Friday till January 5th so a much needed break... So very tired and now this cold to boot ... I'm having a
I have developed overnight the most rotten head cold .. Headache is really bad ..I know inside is all inflamed I can feel it ...eyes are running along with my nose ... We close the business on Friday till January 5th so a much needed break... So very tired and now this cold to boot ... I'm having a
Blackbird8
in
Lung Conditions Community Forum
5 months ago
Your top 7 questions about fall vaccines answered by Your Local Epidemiologist KATELYN JETELINA AUG 29, 2023
Your top 7 questions about fall vaccines answered KATELYN JETELINA AUG 29, 2023 https://yourlocalepidemiologist.substack.com/p/your-top-7-questions-about-fall-vaccines?utm_source=substack&utm_medium=email Thank you for all of your questions! You’re keeping us busy here at YLE. Here are answers to the
Your top 7 questions about fall vaccines answered KATELYN JETELINA AUG 29, 2023 https://yourlocalepidemiologist.substack.com/p/your-top-7-questions-about-fall-vaccines?utm_source=substack&utm_medium=email Thank you for all of your questions! You’re keeping us busy here at YLE. Here are answers to the
lankisterguy
Volunteer
in
CLL Support
9 months ago
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Common Cold and CLL? What does Immune Compromised actually mean?
So when one gets a "common cold," and has CLL progressing but still in W&W, should one expect to get a worse cold than one would've before the CLL took hold? In the 6 years since diagnosis with 13q/unmutated CLL, my numbers have been creeping up, with ALC recently topping at about 30K, and WBC just
So when one gets a "common cold," and has CLL progressing but still in W&W, should one expect to get a worse cold than one would've before the CLL took hold? In the 6 years since diagnosis with 13q/unmutated CLL, my numbers have been creeping up, with ALC recently topping at about 30K, and WBC just
lynnsb6754
in
CLL Support
5 months ago
cold/cough/flu symptoms on day of FET
Hi everyone, just had my 4th FET, no success so far but hoping my recent fallopian tube removal has done the trick and I’ll implant this time 🤞 the annoying thing is after all the failed transfers and last one cancelled when they discovered liquid on my ovary leading to the laproscopy showing a blocked
Hi everyone, just had my 4th FET, no success so far but hoping my recent fallopian tube removal has done the trick and I’ll implant this time 🤞 the annoying thing is after all the failed transfers and last one cancelled when they discovered liquid on my ovary leading to the laproscopy showing a blocked
ToffeeLou
in
Fertility Network UK
5 months ago
Infection without cough or fever?
Is it possible to have a chest infection without a cough or fever? I've just gotten over a cold (2nd one in a month) and again my asthma is flaring but I also feel uncomfortable/pain in the back of my lungs. I don't have a cough, but if I do, it's dry and kind of squeaks. 🤷🏻♀️
Is it possible to have a chest infection without a cough or fever? I've just gotten over a cold (2nd one in a month) and again my asthma is flaring but I also feel uncomfortable/pain in the back of my lungs. I don't have a cough, but if I do, it's dry and kind of squeaks. 🤷🏻♀️
-Butterfly-
in
Asthma Community Forum
5 months ago
More red spots on nails
Still don't know what these are. Anyone else get them?
Still don't know what these are. Anyone else get them?
Brychni
in
NRAS
5 months ago
Sort of flu
I think I’ve got something flu like. I feel achy and horrible, coughing and exhausted. I have been very slowly reducing steroids and am down to 0.5 mg. I’ve been getting shooting pains in one knee and have painful fingers, I’ve never had these particular symptoms before! I don’t know if pmr is flaring
I think I’ve got something flu like. I feel achy and horrible, coughing and exhausted. I have been very slowly reducing steroids and am down to 0.5 mg. I’ve been getting shooting pains in one knee and have painful fingers, I’ve never had these particular symptoms before! I don’t know if pmr is flaring
Yellow-dog
in
PMRGCAuk
5 months ago
Greater susceptibility???
Read this, posted in another group: “BA.2.86 may be more capable of causing infection in people who have previously had COVID-19 or who have received COVID-19 vaccines.” Approved COVID vaccine that may make us more susceptible to the new COVID variant? Good grief!
Read this, posted in another group: “BA.2.86 may be more capable of causing infection in people who have previously had COVID-19 or who have received COVID-19 vaccines.” Approved COVID vaccine that may make us more susceptible to the new COVID variant? Good grief!
Hisue
in
NRAS
9 months ago
no help at all :(
okay here I go I quit alcohol and during the first week the anxiety and depression went off the charts. Crying everyday, staring at floor couldn’t move. It was really bad. Third week started to date I say get a little better and then 5 days ago I got Covid-19. Can you even believe it? So I’ve been getting
okay here I go I quit alcohol and during the first week the anxiety and depression went off the charts. Crying everyday, staring at floor couldn’t move. It was really bad. Third week started to date I say get a little better and then 5 days ago I got Covid-19. Can you even believe it? So I’ve been getting
Overthis1
in
Anxiety and Depression Support
9 months ago
A Fib and Covid.
Hi everyone, I am in the middle of a Covid Infection at the moment and feeling quite poorly. I haven't had an A Fib attack for ages, but am now in the middle of one that has gone on for four hours so far. My question is, have any other members found that Covid has affected their A Fib. Thank you, Jenny
Hi everyone, I am in the middle of a Covid Infection at the moment and feeling quite poorly. I haven't had an A Fib attack for ages, but am now in the middle of one that has gone on for four hours so far. My question is, have any other members found that Covid has affected their A Fib. Thank you, Jenny
Attic
in
AF Association
9 months ago
last tablet
hi today ( Monday ) was my last Venetoclax tablets . It has been a 12 month journey with thank goodness not too much drama . I won’t miss the nausea in the morning that’s for sure and am looking forward to having marmalade again . I just hope I can taste it as after 3 and 1/2 years of escaping covid
hi today ( Monday ) was my last Venetoclax tablets . It has been a 12 month journey with thank goodness not too much drama . I won’t miss the nausea in the morning that’s for sure and am looking forward to having marmalade again . I just hope I can taste it as after 3 and 1/2 years of escaping covid
Hilo13
in
CLL Support
9 months ago
Has anyone succeeded using bluetooth microphone to amplify patients voice so it can be heard on bluetooth hearing aids?
Hi, My wife (78) was diagnosed with PSP about 30 months ago and is in slow decline. Her voice is getting weaker and I am finding it difficult to hear what she says, much of it is mumbled. My hearing aids are bluetooth enabled, so I wondered if anyone had managed to amplify a patient's voice using
Hi, My wife (78) was diagnosed with PSP about 30 months ago and is in slow decline. Her voice is getting weaker and I am finding it difficult to hear what she says, much of it is mumbled. My hearing aids are bluetooth enabled, so I wondered if anyone had managed to amplify a patient's voice using
Legobuilder
in
PSP Association
2 months ago
Time for booster
I’m wondering is it worthwhile getting a booster jab this autumn. I understand covid is still around and my understanding is it’s now milder then previous strains. I have mild asthma(do take a preventer daily), I am 51 and am sitting on the fence on booster number 5. Any thoughts, experiences, those
I’m wondering is it worthwhile getting a booster jab this autumn. I understand covid is still around and my understanding is it’s now milder then previous strains. I have mild asthma(do take a preventer daily), I am 51 and am sitting on the fence on booster number 5. Any thoughts, experiences, those
Saj123456
in
Asthma Community Forum
9 months ago
Got the Covid
I got Fibro after have Lymes for 10 years undiagnosed. I got the lymes treated in the end but was told to keep well away from Covid. Now I've got the Covid. If I do get through all this (I'm in the first week) tell the truth, is it likely to make the fibro worse, cause if so, I need to plan ahead for
I got Fibro after have Lymes for 10 years undiagnosed. I got the lymes treated in the end but was told to keep well away from Covid. Now I've got the Covid. If I do get through all this (I'm in the first week) tell the truth, is it likely to make the fibro worse, cause if so, I need to plan ahead for
dinahdabble
in
Fibromyalgia Action UK
9 months ago
mannitol
mannitol which is in Teva brand of thyroxine and does not agree with everyone. I have found out is obtained by the hydrogenation of sugars from wheat/corn starch no wonder I have problems, being gluten free. Also found it in other medications.
mannitol which is in Teva brand of thyroxine and does not agree with everyone. I have found out is obtained by the hydrogenation of sugars from wheat/corn starch no wonder I have problems, being gluten free. Also found it in other medications.
elwins
in
Thyroid UK
10 months ago
hypothyroid pins and needles in feet
I have been Hypo for 20+ years and since last winter I have pins and needle like pain in my feet. This is almost constant but becomes much worse when cold. Toes are cold to the touch and not pink. Dr has diagnosed Reynards but I’m not sure this is correct as it doesn’t appear in bursts. Does anyone
I have been Hypo for 20+ years and since last winter I have pins and needle like pain in my feet. This is almost constant but becomes much worse when cold. Toes are cold to the touch and not pink. Dr has diagnosed Reynards but I’m not sure this is correct as it doesn’t appear in bursts. Does anyone
Ju17
in
Thyroid UK
5 months ago
Dreaded flu- update its covid
Hi everyone! I hope your all well, thank you for letting me join. Quick history I was born in 1988 with shones syndrome and have had 2 mech valves done now by 35. My 6th surgery in 2018 left me with a stroke, tia and the following year a silent heart attack. My question is with the flu when do I need
Hi everyone! I hope your all well, thank you for letting me join. Quick history I was born in 1988 with shones syndrome and have had 2 mech valves done now by 35. My 6th surgery in 2018 left me with a stroke, tia and the following year a silent heart attack. My question is with the flu when do I need
Mdea1988
in
British Heart Foundation
9 months ago
Rapid Onset of Symptoms
Hello, I was wondering if anyone can help me…. My dad has been diagnosed with PSP only a few months ago but has had symptoms for about 18months. His recent symptoms were textbook stage 2 but quite independent ….. this past Sunday morning he woke up feeling a bit off and then suddenly lost feeling in
Hello, I was wondering if anyone can help me…. My dad has been diagnosed with PSP only a few months ago but has had symptoms for about 18months. His recent symptoms were textbook stage 2 but quite independent ….. this past Sunday morning he woke up feeling a bit off and then suddenly lost feeling in
IPinkie
in
PSP Association
2 months ago
Immunocomprised and suddenly have an asymptomatic Covid infection!
My husband has CLL and is in treatment (finished Obinutuzumab, now on Venetoclax). He has had two pretty severe Covid infections; first one in June 2022, second one in December 22. The second infection turned into long Covid (fatigue, daily low grade fevers) - lasting over six months now. He woke up
My husband has CLL and is in treatment (finished Obinutuzumab, now on Venetoclax). He has had two pretty severe Covid infections; first one in June 2022, second one in December 22. The second infection turned into long Covid (fatigue, daily low grade fevers) - lasting over six months now. He woke up
keikikumu
in
CLL Support
9 months ago
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