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Neomycin / Prednisolone
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Sinus and eye infection
After transplant I experienced multiple sinus infections that I never had before due to be immune suppresion and more recently due to new poor levels of air quality due to climate change, those are becoming more frequent with eye infection as well. My question concerning eye infections. Has anyone had
After transplant I experienced multiple sinus infections that I never had before due to be immune suppresion and more recently due to new poor levels of air quality due to climate change, those are becoming more frequent with eye infection as well. My question concerning eye infections. Has anyone had
Eyak1971
in
Kidney Transplant
8 months ago
Suffering with GCA
Welcome I hope you are fine I have not yet undergone a biopsy or any other examination, but I started taking prednisolone 60 mg and there was a change in the nature of the pain, it became somewhat controlled. Then I reduced the dose to 40 mg, and after a few days I had a relapse and the violent headache
Welcome I hope you are fine I have not yet undergone a biopsy or any other examination, but I started taking prednisolone 60 mg and there was a change in the nature of the pain, it became somewhat controlled. Then I reduced the dose to 40 mg, and after a few days I had a relapse and the violent headache
alinazzal
in
PMRGCAuk
4 hours ago
Phased return
I really appreciate all the support I received from this group recently. Next week will be the last week before I meet with my boss and hr. I've accepted its time for a change and I'm trying not to fear that change. I am currently on 12 mg of prednisolone due to suspected GCA. I've recently been suffering
I really appreciate all the support I received from this group recently. Next week will be the last week before I meet with my boss and hr. I've accepted its time for a change and I'm trying not to fear that change. I am currently on 12 mg of prednisolone due to suspected GCA. I've recently been suffering
Helliwelli12
in
PMRGCAuk
13 hours ago
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Addissons disease
Good afternoon. I was diagnosed with Adison's disease in 2022. Prescribed Prednisolone 5 mg. Now I take hydrocortisone tablets 20 mg per day. Fludrocortisone 0.1 mg. Once a year there is an Adrinal crisis, I end up in intensive care... Constant weakness, no vitality, I sleep a lot... I am only 43
Good afternoon. I was diagnosed with Adison's disease in 2022. Prescribed Prednisolone 5 mg. Now I take hydrocortisone tablets 20 mg per day. Fludrocortisone 0.1 mg. Once a year there is an Adrinal crisis, I end up in intensive care... Constant weakness, no vitality, I sleep a lot... I am only 43
Mariupol
in
PMRGCAuk
17 hours ago
Addissons disease
Good afternoon. I was diagnosed with Adison's disease in 2022. Prescribed Prednisolone 5 mg. Now I take hydrocortisone tablets 20 mg per day. Fludrocortisone 0.1 mg. Once a year there is an Adrinal crisis, I end up in intensive care... Constant weakness, no vitality, I sleep a lot... I am only 43
Good afternoon. I was diagnosed with Adison's disease in 2022. Prescribed Prednisolone 5 mg. Now I take hydrocortisone tablets 20 mg per day. Fludrocortisone 0.1 mg. Once a year there is an Adrinal crisis, I end up in intensive care... Constant weakness, no vitality, I sleep a lot... I am only 43
Mariupol
in
PMRGCAuk
17 hours ago
Hydroxychloroquine toxic retinopathy
Hi. I have had Lupus for 22 years and been on Hydroxychloroquine 400mg daily since then plus 2mg Prednisolone. Recent eye tests have shown that the Hydroxy is affecting the retina. I was warned at the outset, that it can affect eyes, but it still a bit of a shock. Opthamology Consultant says I must
Hi. I have had Lupus for 22 years and been on Hydroxychloroquine 400mg daily since then plus 2mg Prednisolone. Recent eye tests have shown that the Hydroxy is affecting the retina. I was warned at the outset, that it can affect eyes, but it still a bit of a shock. Opthamology Consultant says I must
Juniperm
in
LUPUS UK
19 hours ago
Steroid rash
I've been taking Prednisolone for a year and have developed a red itchy steroid rash on my face. Can it be managed naturally without running off to the surgery. I use make up when I go anywhere but I wonder if that irritates it further. I am reducing my Pred. but I'm on 9mg still.
I've been taking Prednisolone for a year and have developed a red itchy steroid rash on my face. Can it be managed naturally without running off to the surgery. I use make up when I go anywhere but I wonder if that irritates it further. I am reducing my Pred. but I'm on 9mg still.
BinnieBoo
in
PMRGCAuk
1 day ago
My Music, Your Music, Our Music
Hello Again, I have only written once before ( my introduction ) where I confessed to being a tapering Idiot for speeding up the reduction way too fast. I blamed my inner 18 year old boy and his ridiculous optimism and devil may care attitude. I am a little bit like Billy Connelly as I wander off
Hello Again, I have only written once before ( my introduction ) where I confessed to being a tapering Idiot for speeding up the reduction way too fast. I blamed my inner 18 year old boy and his ridiculous optimism and devil may care attitude. I am a little bit like Billy Connelly as I wander off
Willpower1945
in
PMRGCAuk
1 day ago
Is it PMR?
Hi. Diagnosed with PMR several years ago and had flare ups along the way. GP trying to reduce prednisolone dosage again, currently about to go down to 8mg. which isn't touching the pain. However I'm now wondering if in fact I have fibromyalgia. I've been doing some research on Dr Google and have just
Hi. Diagnosed with PMR several years ago and had flare ups along the way. GP trying to reduce prednisolone dosage again, currently about to go down to 8mg. which isn't touching the pain. However I'm now wondering if in fact I have fibromyalgia. I've been doing some research on Dr Google and have just
Everett19
in
PMRGCAuk
2 days ago
Polymyalgia and Fibromyalgia
I have been taking prednisolone for a long time for polymyalgia and GCA. The rheumatologist has decided to take me off prednisolone ( slowly reducing) and putting me on to methotrexate, as she said that prednisolone can affect my bones.Since I stopped taking prednisolone I have been getting all the symptoms
I have been taking prednisolone for a long time for polymyalgia and GCA. The rheumatologist has decided to take me off prednisolone ( slowly reducing) and putting me on to methotrexate, as she said that prednisolone can affect my bones.Since I stopped taking prednisolone I have been getting all the symptoms
Chrismag
in
PMRGCAuk
3 days ago
Fatigue !
Diagnosed with PMR in 2021, struggled like everyone and have now completely come off Prednisolone. I’m still getting days with hip and neck and shoulder pain but the worst is the fatigue. Some days I’m fine but mostly feel exhausted. Since stopping Pred my sleep isn’t good. Is it ok to have the occasional
Diagnosed with PMR in 2021, struggled like everyone and have now completely come off Prednisolone. I’m still getting days with hip and neck and shoulder pain but the worst is the fatigue. Some days I’m fine but mostly feel exhausted. Since stopping Pred my sleep isn’t good. Is it ok to have the occasional
Blackberrybush
in
PMRGCAuk
3 days ago
Norovirus - does having PMR increase my risk?
I am currently on 5.5 mg prednisolone. The Care Home where I work part time has an outbreak of Norovirus with a lot of the residents and staff being infected, am I more at risk because of my PMR and steroid dependency?
I am currently on 5.5 mg prednisolone. The Care Home where I work part time has an outbreak of Norovirus with a lot of the residents and staff being infected, am I more at risk because of my PMR and steroid dependency?
Mfaepink1973
in
PMRGCAuk
3 days ago
flare up
I have had a flare of symptoms over past few days. I have had PMR for nine years and have seldom been below 5 mg of prednisolone. I have increased to 10 yesterday and today, how many days can I do this and be able to go back to 5 safely. I am going on a 10 day holiday on Wednesday so I want to feel
I have had a flare of symptoms over past few days. I have had PMR for nine years and have seldom been below 5 mg of prednisolone. I have increased to 10 yesterday and today, how many days can I do this and be able to go back to 5 safely. I am going on a 10 day holiday on Wednesday so I want to feel
Jeanlindenburn
in
PMRGCAuk
3 days ago
Covid and injections
I suffered from Covid over Christmas from the 16th to the 30th December. Up 'til now I have had all the injections on offer. I read Dorset Lady's post that we are going to be offered another injection in the spring. It has left me wondering whether I will need this or not in the circumstances. I
I suffered from Covid over Christmas from the 16th to the 30th December. Up 'til now I have had all the injections on offer. I read Dorset Lady's post that we are going to be offered another injection in the spring. It has left me wondering whether I will need this or not in the circumstances. I
prunus
in
PMRGCAuk
3 days ago
Flare but wasn't
Hello :) I have been on Prednisolone since 2013 for GCA/PMR I was down to 9mg and I had what I thought was a flare spoke to gp via phone and he said I could up to 15mg for 1 week then 12mg for 1 week then 10mg for 1 week then back to 9mg as my hands are now back to normal I would like to get back to
Hello :) I have been on Prednisolone since 2013 for GCA/PMR I was down to 9mg and I had what I thought was a flare spoke to gp via phone and he said I could up to 15mg for 1 week then 12mg for 1 week then 10mg for 1 week then back to 9mg as my hands are now back to normal I would like to get back to
suszannah
in
PMRGCAuk
3 days ago
Lercandipine 20mg and AFib
I was started on 10mg Lercandipine in the mornings by my Cardiologist about a year ago. I also take 15mg Bisoprol, 2.5mg Indapamide and 40 mg Olmesartan together with 60mg Edoxaban in the morning and 8mg Doxazosin at night. A week ago he changed my Lercandipine dosage to 20mg and to take it in the evening
I was started on 10mg Lercandipine in the mornings by my Cardiologist about a year ago. I also take 15mg Bisoprol, 2.5mg Indapamide and 40 mg Olmesartan together with 60mg Edoxaban in the morning and 8mg Doxazosin at night. A week ago he changed my Lercandipine dosage to 20mg and to take it in the evening
Jomaur
in
Atrial Fibrillation Support
5 days ago
Headaches!
Hi everyone.....I'm started my PMR journey middle of January so have only been on Prednisolone for 6 weeks... I started on 20mg and now on 10mg I did up dosage for 2 weeks so was taking 12mg because I felt poorly... But my question is I've had a headache almost constantly for weeks....is it the press
Hi everyone.....I'm started my PMR journey middle of January so have only been on Prednisolone for 6 weeks... I started on 20mg and now on 10mg I did up dosage for 2 weeks so was taking 12mg because I felt poorly... But my question is I've had a headache almost constantly for weeks....is it the press
Tescohednesford
in
PMRGCAuk
6 days ago
Feeling dreadful but doc says results are fine!
Hi there, I was diagnosed with underactive thyroid back in July 2020. I was prescribed 25mg levothyroxine which was increased to 50mg after 6 months. Shortly after starting levothyroxine I started getting stiffness in my neck and shoulders along with pain in my hips and groin - the only way I can
Hi there, I was diagnosed with underactive thyroid back in July 2020. I was prescribed 25mg levothyroxine which was increased to 50mg after 6 months. Shortly after starting levothyroxine I started getting stiffness in my neck and shoulders along with pain in my hips and groin - the only way I can
FlamingoPenguin
in
Thyroid UK
7 days ago
Rheumatology appointment update
Hi All, Hope you're all well/well as expected. Just thought I would update on my situation as I saw Dr Cheung again today for a follow up. Those who have been following will know I have had a few issues after having been diagnosed with PMR in December '23 I had to up my dose of prednisolone to 15mg
Hi All, Hope you're all well/well as expected. Just thought I would update on my situation as I saw Dr Cheung again today for a follow up. Those who have been following will know I have had a few issues after having been diagnosed with PMR in December '23 I had to up my dose of prednisolone to 15mg
Paulx222
in
PMRGCAuk
8 days ago
persistent oral thrush
I've been on an increased dose of prednisolone since August last year. I've started reducing since January (tried before with a flare-up). I also use a steroid inhaler for asthma (and rinse afterwards). I have frequent problems with oral thrush. Unfortunately the stuff that seemed to work best - the
I've been on an increased dose of prednisolone since August last year. I've started reducing since January (tried before with a flare-up). I also use a steroid inhaler for asthma (and rinse afterwards). I have frequent problems with oral thrush. Unfortunately the stuff that seemed to work best - the
oldtimer2
in
NRAS
8 days ago
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