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Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
Very interesting article: [u]
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
[/u]
2024
https://www.gilmorehealth.com/tetanus-vaccine-decreases-incidence-of-parkinsons-disease-and-slows-its-progression/ It is based on this paper: [u]
Tetanus vaccination
Very interesting article: [u]
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
[/u]
2024
https://www.gilmorehealth.com/tetanus-vaccine-decreases-incidence-of-parkinsons-disease-and-slows-its-progression/ It is based on this paper: [u]
Tetanus vaccination
Bolt_Upright
in
Cure Parkinson's
4 days ago
Infections like pneumonia and sinus. Lessons learned.
I’m saddened and sorry for all those who have been suffering from pneumonia and respiratory infections. Been posted of late. As a physician who knows better, I wish I’d followed my on advice to do ALL of the following 1. Test right away for COVID 2. Get a complete viral nasal swab to be tested
I’m saddened and sorry for all those who have been suffering from pneumonia and respiratory infections. Been posted of late. As a physician who knows better, I wish I’d followed my on advice to do ALL of the following 1. Test right away for COVID 2. Get a complete viral nasal swab to be tested
skipro
in
CLL Support
6 days ago
visual snow and fibromyalgia
does anyone have strange vision. I see eye floaters all day and when I close my eyes but this has also developed into what I can only describe as black and white static vision. I’ve have issues with my eyelids not automatically opening too. Migraines are most likely linked but not the reason. It’s bizarre
does anyone have strange vision. I see eye floaters all day and when I close my eyes but this has also developed into what I can only describe as black and white static vision. I’ve have issues with my eyelids not automatically opening too. Migraines are most likely linked but not the reason. It’s bizarre
Loobyloo1966
in
Fibromyalgia Action UK
9 months ago
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Dry mouth and throat
I have a constantly dry throat and meds, probably from meds. Other than carrying water around with me whenever I go out, or a constant supply of cough sweets, does anyone have any suggestions? Thanks
I have a constantly dry throat and meds, probably from meds. Other than carrying water around with me whenever I go out, or a constant supply of cough sweets, does anyone have any suggestions? Thanks
veggiefan70
in
Fibromyalgia Action UK
6 months ago
covid afibs???/
I had covid in September of 2023 and soon thereafter developed a fibs, which I have never had in my life! I am 69. My question is this: Has this happened to anyone else and did they eventually go away, or is it a permanent thing?
I had covid in September of 2023 and soon thereafter developed a fibs, which I have never had in my life! I am 69. My question is this: Has this happened to anyone else and did they eventually go away, or is it a permanent thing?
peachtreepiggy
in
Atrial Fibrillation Support
3 months ago
White Blood Cells
Second urine test showing White Blood Cells elevated, no UTI anyone had this before
Second urine test showing White Blood Cells elevated, no UTI anyone had this before
mydishnow
in
NRAS
5 months ago
Covid vaccine
I am going to put it out there . Did anyone get ill with encephalitis after taking the Covid vaccine? This has been something that has been playing in my mind for a while My mom was in later 60s in good health and active before having the vaccine.
I am going to put it out there . Did anyone get ill with encephalitis after taking the Covid vaccine? This has been something that has been playing in my mind for a while My mom was in later 60s in good health and active before having the vaccine.
GIL910
in
Encephalitis Society
3 months ago
Tapering - have I got it wrong?
Hi. I am a new member and this is my first post. Diagnosed with PMR in March 2023, started on 15mg of pred on 31st March. It worked like a dream and within 48 hrs, my pain was down 70% and my energy was up 70%. I felt fantastic and within a month started slowly to increase my level of exercise and activity
Hi. I am a new member and this is my first post. Diagnosed with PMR in March 2023, started on 15mg of pred on 31st March. It worked like a dream and within 48 hrs, my pain was down 70% and my energy was up 70%. I felt fantastic and within a month started slowly to increase my level of exercise and activity
EnyaBlue
in
PMRGCAuk
9 months ago
Paxlovid for “mild” COVID?
hello all. Just wondering what your experiences have been regarding taking Paxlovid. I realize you can’t advise but I would love to hear from fellow immune suppressed types like me. I have taken it before but when I had it last year I felt pretty bad and taking the Paxlovid was a no brainer. This time
hello all. Just wondering what your experiences have been regarding taking Paxlovid. I realize you can’t advise but I would love to hear from fellow immune suppressed types like me. I have taken it before but when I had it last year I felt pretty bad and taking the Paxlovid was a no brainer. This time
Bon1
in
NRAS
3 months ago
Back to square one
Hi, I first started having coughing problems back in November 2022 when I caught what I thought was just a bad cold or covid, I was getting phlegm stuck in my airways which was tough to get out when coughing, and sometimes I struggled to breath. Sometimes to the point where I actually cried because
Hi, I first started having coughing problems back in November 2022 when I caught what I thought was just a bad cold or covid, I was getting phlegm stuck in my airways which was tough to get out when coughing, and sometimes I struggled to breath. Sometimes to the point where I actually cried because
amygx25
in
Asthma Community Forum
3 months ago
COPD and Pneumonia
Hello. My mom has severe COPD and got out of the hospital last week after a 3 week stay for pneumonia. She’s had COPD for 16 years and just went on O2 about a year ago. She’s always done well with the COPD and never had an exacerbation until the pneumonia. I know it can take a very long time for the
Hello. My mom has severe COPD and got out of the hospital last week after a 3 week stay for pneumonia. She’s had COPD for 16 years and just went on O2 about a year ago. She’s always done well with the COPD and never had an exacerbation until the pneumonia. I know it can take a very long time for the
nyla668
in
Lung Conditions Community Forum
1 month ago
COVID-19
Been battling Covid for 17 days. I am negative but have a lot of physical issues achy big time. Always exhausted. No motivation. Starting to take a toll on me mentally. Doctor says that sometimes it takes weeks or months to get rid of everything. I hate feeling like this
Been battling Covid for 17 days. I am negative but have a lot of physical issues achy big time. Always exhausted. No motivation. Starting to take a toll on me mentally. Doctor says that sometimes it takes weeks or months to get rid of everything. I hate feeling like this
Trainchaser
in
Anxiety and Depression Support
3 months ago
COVID & sulfasalazine?
After all these years hubby has passed COVID to me! Contacted GP, they have referred me to respiratory@home still waiting for them to call. Question is do I keep taking sulfasalazine.? I've called my Rheumy helpline but they've not got back to me and I've looked on here but can't find anything saying
After all these years hubby has passed COVID to me! Contacted GP, they have referred me to respiratory@home still waiting for them to call. Question is do I keep taking sulfasalazine.? I've called my Rheumy helpline but they've not got back to me and I've looked on here but can't find anything saying
Haz58
in
NRAS
3 months ago
COPD and Long Covid
Hi all, I've been ill for over three years with Long Covid and just last week diagnosed with COPD stage 2. Looking through my medical history COPD was mentioned back in 2005, but I was told it was Asthma! Just joined my local Breathe Easy group who are great and very supportive.
Hi all, I've been ill for over three years with Long Covid and just last week diagnosed with COPD stage 2. Looking through my medical history COPD was mentioned back in 2005, but I was told it was Asthma! Just joined my local Breathe Easy group who are great and very supportive.
SimonJJJ
in
Lung Conditions Community Forum
3 months ago
Covid - Reflux
Just out of interest has anyone's reflux problems come on after having Covid? I had it back in early December and got problems in middle of January. I have read somewhere that there could be a link .
Just out of interest has anyone's reflux problems come on after having Covid? I had it back in early December and got problems in middle of January. I have read somewhere that there could be a link .
Pinkcatfairy
in
Acid Reflux Support
3 months ago
I thought it was just a cold!
Not on ocrevus anymore, but I had the 1st of my monthly tysabri on the 20th, and I've since got a chest infection 😞 a couple of nights of not being able to sleep properly had really affected me, to the point where on Monday just gone I was wanting to get in to see a GP! But, when I called them up, they
Not on ocrevus anymore, but I had the 1st of my monthly tysabri on the 20th, and I've since got a chest infection 😞 a couple of nights of not being able to sleep properly had really affected me, to the point where on Monday just gone I was wanting to get in to see a GP! But, when I called them up, they
Cwright170994
in
My MSAA Community
6 months ago
What would be your Low Dose Naltrexone (LDN) dosing recommendation for long Covid and Mast Cell Activation?
What would be your Low Dose Naltrexone (LDN) dosing recommendation for long Covid and Mast Cell Activation? Answered by Sebastian Denison, RPh https://youtu.be/w5RLJy34ArU
What would be your Low Dose Naltrexone (LDN) dosing recommendation for long Covid and Mast Cell Activation? Answered by Sebastian Denison, RPh https://youtu.be/w5RLJy34ArU
Shewulf
Administrator
in
LDN Research Trust
3 months ago
Bloating - Zoladex/Tibolone
Hi I have been on Zoladex injections for a year now and have had add back HRT (tibolone) for about 6 weeks.The add back HRT has really helped the hot flushes & muscle pain but over the past 2 weeks I have been suffering with awful bloating which increases when I eat or drink anything. Has anybody else
Hi I have been on Zoladex injections for a year now and have had add back HRT (tibolone) for about 6 weeks.The add back HRT has really helped the hot flushes & muscle pain but over the past 2 weeks I have been suffering with awful bloating which increases when I eat or drink anything. Has anybody else
Bookish_Girl
in
Endometriosis UK
25 days ago
Raised Blood Pressure after Covid
Not sure if this is the right Forum to post this on but I wondered if anyone who has high blood pressure and has had Covid has found that their blood pressure readings have risen since having it. I had an appointment with my Cardiologist this morning and showed him my readings over the last month orso
Not sure if this is the right Forum to post this on but I wondered if anyone who has high blood pressure and has had Covid has found that their blood pressure readings have risen since having it. I had an appointment with my Cardiologist this morning and showed him my readings over the last month orso
Jomaur
in
Atrial Fibrillation Support
3 months ago
Finally, we may have found the smoking gun.
We had been able to put it aside, and the hospital agreed they had made a mistake when they said Margaret had Cirrhosis. And was, in fact, NASH with Grade 1 fibrosis. Still, NASH was a surprise, as Magaret was a nondrinker, not obese, and had no health conditions that would even be considered for
We had been able to put it aside, and the hospital agreed they had made a mistake when they said Margaret had Cirrhosis. And was, in fact, NASH with Grade 1 fibrosis. Still, NASH was a surprise, as Magaret was a nondrinker, not obese, and had no health conditions that would even be considered for
ceward204
in
British Liver Trust
3 months ago
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