Search
Search
About
Log in
Join
Experiences with
Genital tract infections
Posts
Communities
29,530 public posts
Filter results
Timings of meds.
Can anyone advise me on taking Levo .I take statins at night.Levo and lansoperazol before breakfast.Apixaban 12 hours apart 8.30 am and pm .with the 8.30 Apixaban in the morning I take blood pressure meds.Its just impossible to have 4 hour gaps with this lot of meds ,I'm so confused.I have had this regime
Can anyone advise me on taking Levo .I take statins at night.Levo and lansoperazol before breakfast.Apixaban 12 hours apart 8.30 am and pm .with the 8.30 Apixaban in the morning I take blood pressure meds.Its just impossible to have 4 hour gaps with this lot of meds ,I'm so confused.I have had this regime
ETHEL103
in
Thyroid UK
1 year ago
slightly anxious and just looking for moral support
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Abcd123455
in
PMRGCAuk
8 months ago
Starting Pegasys soon
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
IsabelleHo
in
MPN Voice
8 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
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 International
6 months ago
Lymphedema & Knee bursitis
I have Inflammatory arthritis, Sjogren's and OA. I have been on Methotrexate and Imraldi since 2017, before that I was on Benepali. I have had a new hip in 2017 and I also suffered with my knees which despite many steroid injections they are no longer having any effect. I saw my rheumatologist
I have Inflammatory arthritis, Sjogren's and OA. I have been on Methotrexate and Imraldi since 2017, before that I was on Benepali. I have had a new hip in 2017 and I also suffered with my knees which despite many steroid injections they are no longer having any effect. I saw my rheumatologist
Bailybiscuit
in
NRAS
6 months ago
Hip Replacement while on treatment??
My husband, who is in a Clinical Trial at MDA for Richter's, needs a hip replacement badly - such that his severe arthritis is a bigger deal to his quality of life than the Richter's. He saw an orthopedic pain management specialist last week who had nothing to offer, stating that a steroid injection
My husband, who is in a Clinical Trial at MDA for Richter's, needs a hip replacement badly - such that his severe arthritis is a bigger deal to his quality of life than the Richter's. He saw an orthopedic pain management specialist last week who had nothing to offer, stating that a steroid injection
laurieq
in
CLL Support
6 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
6 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
6 months ago
What to do after prednisolone rescue ended?
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Merryroundabout
in
Asthma Community Forum
8 months ago
Germantara
I've getting my medical summary from doctors cause as you know I'm doing pip had fantastic advice and would like to thank everyone Well I was looking at it and some I didn't understand so I googled them the copd stage I'm at I'm end stage 3 it said I've got 5 to 8 years to live I thought
I've getting my medical summary from doctors cause as you know I'm doing pip had fantastic advice and would like to thank everyone Well I was looking at it and some I didn't understand so I googled them the copd stage I'm at I'm end stage 3 it said I've got 5 to 8 years to live I thought
Germantara
in
Lung Conditions Community Forum
1 year ago
awful cough before transfer- can I take anything?
Hello everyone, I hope everyone is doing ok on their journey. I have my transfer on Monday morning and have the worst cough I’ve ever had, it’s so chesty and painful. I just wondered if I could take some cough medicine or anything in advance of transfer or if it will affect my lining or chances? I
Hello everyone, I hope everyone is doing ok on their journey. I have my transfer on Monday morning and have the worst cough I’ve ever had, it’s so chesty and painful. I just wondered if I could take some cough medicine or anything in advance of transfer or if it will affect my lining or chances? I
Daisy-Delilah
in
Fertility Network UK
1 year ago
ADT and crying
Does anyone else that has been on ADT drugs for years have trouble with tears or crying for no real reason? I tear up anymore at just the thought of something sad. It’s a major pain in the ass, not to mention embarrassing because I am still employed. Wondering if there is a solution other than stopping
Does anyone else that has been on ADT drugs for years have trouble with tears or crying for no real reason? I tear up anymore at just the thought of something sad. It’s a major pain in the ass, not to mention embarrassing because I am still employed. Wondering if there is a solution other than stopping
joeguy
in
Advanced Prostate Cancer
8 months ago
Runny
My nose keeps running and I have to cough to clear throat what can it be?
My nose keeps running and I have to cough to clear throat what can it be?
amberrose2
in
PSP Association
1 year ago
GPA flare, is it likely even if I only have 1 symptom
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
stuc
in
Vasculitis UK
8 months ago
enlarged sore breasts
hi - rather embarrassing but here goes! Approximately 2 weeks ago I had to increase levothyroxine to 100 mcgs- breasts are now enlarged and sore. I can’t be pregnant- I happen to of had routine breast scan just prior to meds increase and no abnormalities detected. Has anyone else experienced this
hi - rather embarrassing but here goes! Approximately 2 weeks ago I had to increase levothyroxine to 100 mcgs- breasts are now enlarged and sore. I can’t be pregnant- I happen to of had routine breast scan just prior to meds increase and no abnormalities detected. Has anyone else experienced this
Purplepuffin
in
Thyroid UK
8 months 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
6 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
6 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
6 months ago
Covid
Does a head cold stop you taking covid ? My husband and my son has covid they thought it was only cold , they had it several days before they tested . I've been testing every day since as I'm on methotrexate and remsima, my tests are clear so far . I have not had my covid vaccine yet, but I have
Does a head cold stop you taking covid ? My husband and my son has covid they thought it was only cold , they had it several days before they tested . I've been testing every day since as I'm on methotrexate and remsima, my tests are clear so far . I have not had my covid vaccine yet, but I have
Grounsel
in
NRAS
10 months ago
Wife getting MMR vaccine booster - isolate or not?
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
xpro3
in
CLL Support
5 months ago
1
...
46
47
48
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Lung Conditions Community Forum
2987 results
Fertility Network UK
2841 results
NRAS
2401 results
View top 10 communities
Sort by
Most Relevant
Newest