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Neomycin / Prednisolone
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giant Cell
I’m off Prednisone and on Actemra only now. I inject it once a week. Lately been feeling a little light headed and woozy. My blood pressure is fine!
I’m off Prednisone and on Actemra only now. I inject it once a week. Lately been feeling a little light headed and woozy. My blood pressure is fine!
LRevell
in
PMRGCAuk
5 months ago
Experiences with securing ss and private disability
Hello, Silent observor here, wife to Ed: Diagnosed with stage IV, Gleason 8, November 2020, with mets to nearby lymph nodes and lungs (of all places). Successfully treated so far with orchiectomy, Zytiga and prednisone with minimum SE. Age 60, living in PNW of US. Ed is considering an application
Hello, Silent observor here, wife to Ed: Diagnosed with stage IV, Gleason 8, November 2020, with mets to nearby lymph nodes and lungs (of all places). Successfully treated so far with orchiectomy, Zytiga and prednisone with minimum SE. Age 60, living in PNW of US. Ed is considering an application
MIkamom
in
Advanced Prostate Cancer
5 months ago
Pain-paralysis-neuropathy!?!?
I am on Leflunomide. Normally I’m fine. The last month I have had inflammation in my eyes, my wrists have been weak. Prednisone daily has made it tolerable. Last night I woke up with my left hand totally numb and on fire. So painful. I’m not sure what is going on. …anyone have this happen? The doctor
I am on Leflunomide. Normally I’m fine. The last month I have had inflammation in my eyes, my wrists have been weak. Prednisone daily has made it tolerable. Last night I woke up with my left hand totally numb and on fire. So painful. I’m not sure what is going on. …anyone have this happen? The doctor
Nana-8
in
NRAS
5 months ago
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Update
Hi everyone, it’s been a while. I’ve had a very long journey involving numerous hospital admissions and investigations into why I’ve got pleural/pericardial effusion’s and although my respiratory we’re saying connective tissue disease, the rheumatologist I seen wasn’t fully onboard as my ANA is negative
Hi everyone, it’s been a while. I’ve had a very long journey involving numerous hospital admissions and investigations into why I’ve got pleural/pericardial effusion’s and although my respiratory we’re saying connective tissue disease, the rheumatologist I seen wasn’t fully onboard as my ANA is negative
Numptybrain
in
Lung Conditions Community Forum
5 months ago
Any proof that removing a tumor off prostate bed by radiation or surgery is better than just systemic therapy ?
Here is my history PSA rising now 0.77 Going for pet scan tomorrow Tumour on prostate bed had Radical Prostatectomy with Lymph node removal 03/2023 Stage 4 Oligo Metastatic Prostate Cancer Original PSA 942.40 at diagnosis 06/2022 Gleason 8 / 9 ductal without large cribform gland, cT3b
Here is my history PSA rising now 0.77 Going for pet scan tomorrow Tumour on prostate bed had Radical Prostatectomy with Lymph node removal 03/2023 Stage 4 Oligo Metastatic Prostate Cancer Original PSA 942.40 at diagnosis 06/2022 Gleason 8 / 9 ductal without large cribform gland, cT3b
Shorehousejam
in
Advanced Prostate Cancer
5 months ago
Help I don’t understand
So for the last 4 months I’ve been having pain in my muscles and head as well as tingling and a burning sensation. Also extreme fatigue and a red rash on my cheeks and trouble swallowing.My doctor gave me prednisone to treat because crp and esr were high. She also started me on plaquenil. Now before
So for the last 4 months I’ve been having pain in my muscles and head as well as tingling and a burning sensation. Also extreme fatigue and a red rash on my cheeks and trouble swallowing.My doctor gave me prednisone to treat because crp and esr were high. She also started me on plaquenil. Now before
Jadaboo4
in
LUPUS UK
5 months ago
lower dose prednisone
Update Took a call from respiratory nurse an hour ago. My respiratory consultant and rheumatologist have had a discussion and decided to keep me on 10 mg of prednisone until I see rheumatologist in June instead of stopping in may as planned as it’s obviously working providing this was a connective tissue
Update Took a call from respiratory nurse an hour ago. My respiratory consultant and rheumatologist have had a discussion and decided to keep me on 10 mg of prednisone until I see rheumatologist in June instead of stopping in may as planned as it’s obviously working providing this was a connective tissue
Numptybrain
in
PMRGCAuk
5 months ago
PMR or Arthritis?
I have been reading your forum since I was diagnosed with PMR just over 2 years ago. I have found it incredibly informative, helpful and comforting, but this is my 1st post. I was diagnosed with PMR after a couple of months of extreme pain and stiffness in the neck, shoulders hips and knee, to the extent
I have been reading your forum since I was diagnosed with PMR just over 2 years ago. I have found it incredibly informative, helpful and comforting, but this is my 1st post. I was diagnosed with PMR after a couple of months of extreme pain and stiffness in the neck, shoulders hips and knee, to the extent
Reneestpierre
in
PMRGCAuk
9 months ago
Prednisone for treatment of AIG
I've just been started on Prednisone or Prednisolone, immunosuppressant steroids, for treatment of Autoimmune Gastritis/autoimmune PA. This has recently, within the last few years been shown to possibly heal AIG, although not entirely cure. It is also used to prevention immune system rejection of organ
I've just been started on Prednisone or Prednisolone, immunosuppressant steroids, for treatment of Autoimmune Gastritis/autoimmune PA. This has recently, within the last few years been shown to possibly heal AIG, although not entirely cure. It is also used to prevention immune system rejection of organ
Rexz
in
Pernicious Anaemia Society
7 months ago
Insomnia
Since removing Prednisone and adding instead Dexamethasone medication at 1-mg to go with Zytiga I have a very hard time with insomnia. Any suggestions. Only able to sleep about 4 hours daily.
Since removing Prednisone and adding instead Dexamethasone medication at 1-mg to go with Zytiga I have a very hard time with insomnia. Any suggestions. Only able to sleep about 4 hours daily.
Poollover
in
Advanced Prostate Cancer
5 months ago
GCA Questions
Hi Kind Friends, My GCA hit last October, about 6 months ago, and I was put on 60 mg. Prednisone. (I’ve also been on Actemra since November.) I’m doing pretty well, but I wanted to check in regarding my tapering. I’m down to 8 mg. (from 9, about a week ago), and will have stayed there 1 month when
Hi Kind Friends, My GCA hit last October, about 6 months ago, and I was put on 60 mg. Prednisone. (I’ve also been on Actemra since November.) I’m doing pretty well, but I wanted to check in regarding my tapering. I’m down to 8 mg. (from 9, about a week ago), and will have stayed there 1 month when
Lenore58
in
PMRGCAuk
5 months ago
Diabetes and Prednisolone
Hi, just enquiring about the use of Prednisolone and its affect on diabeties. I have been a type 2 diabetic since 2016. For the first four years I managed to control it by diet only but since I was diagnosed with PMR in August 2020 my diabetes has got worse year on year. I was initially put on Metformin
Hi, just enquiring about the use of Prednisolone and its affect on diabeties. I have been a type 2 diabetic since 2016. For the first four years I managed to control it by diet only but since I was diagnosed with PMR in August 2020 my diabetes has got worse year on year. I was initially put on Metformin
Tiggy70
in
PMRGCAuk
7 months ago
3 Abiraterone tabs in place of 4.
Warriors Some time back I posted that my MO had told me to take 3 Abiraterone tablets with 5 mg Prednisone daily instead of 4 to help with an out of control Blood Pressure problem. I was worried (as were some of the responses) that this could impact the ADT therapy. Recently had blood work done
Warriors Some time back I posted that my MO had told me to take 3 Abiraterone tablets with 5 mg Prednisone daily instead of 4 to help with an out of control Blood Pressure problem. I was worried (as were some of the responses) that this could impact the ADT therapy. Recently had blood work done
85236442968
in
Advanced Prostate Cancer
5 months ago
prednisone
It’s been years since I’ve been on prednisone and then I was on dosages of 40/30mg per day for brittle asthma but now it’s for pleural/pericardial effusion and I’ve reduced from 29 to 15 mg my 2nd week I feel extremely short of breath my ankles and wrists still hurt so does my lumbar back which hurt
It’s been years since I’ve been on prednisone and then I was on dosages of 40/30mg per day for brittle asthma but now it’s for pleural/pericardial effusion and I’ve reduced from 29 to 15 mg my 2nd week I feel extremely short of breath my ankles and wrists still hurt so does my lumbar back which hurt
Numptybrain
in
PMRGCAuk
5 months ago
incorrect dose of prednisolone?
Just less than a month ago, I reduced my first prednisolone dose from 15mg to 12.5mg. This was after a blood test. I wasn’t keen to reduce by more than ten percent, especially as I was going to be travelling a long way and be away for Xmas and new year, then home for two days and away again for eight
Just less than a month ago, I reduced my first prednisolone dose from 15mg to 12.5mg. This was after a blood test. I wasn’t keen to reduce by more than ten percent, especially as I was going to be travelling a long way and be away for Xmas and new year, then home for two days and away again for eight
Freshairfiend
in
PMRGCAuk
9 months ago
Tooth extraction and Prednisolone
First, thank you for all the fantastic help and advice...now my question. 9 months post diagnosis and (mainly) tapering well from 15mg to 9mg.In a day or so, I need to have a tooth removed. 63 and with "my generation" teeth. The dentist has advised to double dose on the day of the procedure. That seems
First, thank you for all the fantastic help and advice...now my question. 9 months post diagnosis and (mainly) tapering well from 15mg to 9mg.In a day or so, I need to have a tooth removed. 63 and with "my generation" teeth. The dentist has advised to double dose on the day of the procedure. That seems
Zak61
in
PMRGCAuk
9 months ago
The Flare That Keeps on Giving
I was diagnosed with PMR in August, 2022. I also have multiple sclerosis, autoimmune thyroid disease (Grave’s) and Sjogren’s Disease. With a few ups and downs when I had to temporarily increase the dose before dropping back to just above where I had been before the flare, my taper using DL’s slow 5 week
I was diagnosed with PMR in August, 2022. I also have multiple sclerosis, autoimmune thyroid disease (Grave’s) and Sjogren’s Disease. With a few ups and downs when I had to temporarily increase the dose before dropping back to just above where I had been before the flare, my taper using DL’s slow 5 week
Donna5658
in
PMRGCAuk
5 months ago
Travel Insurance with GPA
Need to get Travel Insurance for Europe this year. Any recommendations ? Had a look at previous posts...anybody had a positive experience with a company when a claim was made ? RTX Infusion, one so far. Methotrexate and 2mg Prednisolone daily Thanks
Need to get Travel Insurance for Europe this year. Any recommendations ? Had a look at previous posts...anybody had a positive experience with a company when a claim was made ? RTX Infusion, one so far. Methotrexate and 2mg Prednisolone daily Thanks
Bailey59
in
Vasculitis UK
9 months ago
Struggling with Mycophenolate
Hi all, do any of you take Nintedanib with Prednisolone? My consultant has been trying to get me onto Mycophenolate before starting me on Nintedanib , as it is steroid sparing,but I hate feeling the way I do on this drug. Constant nausea, low mood ( I don’t feel like me at all) disrupted sleep and low
Hi all, do any of you take Nintedanib with Prednisolone? My consultant has been trying to get me onto Mycophenolate before starting me on Nintedanib , as it is steroid sparing,but I hate feeling the way I do on this drug. Constant nausea, low mood ( I don’t feel like me at all) disrupted sleep and low
Blyth1
in
Lung Conditions Community Forum
9 months ago
Mycophenolate instead of Perfinedine or Nintenanib?
Hi everyone I became breathless suddenly in August 2023. This was initially dismissed by my GP even though O2 was 90% as my chest was clear and I had no cough. A fortnight later I was able to get an appointment with a different GP who sent me for a chest X ray which showed I had pulmonary fibrosis.
Hi everyone I became breathless suddenly in August 2023. This was initially dismissed by my GP even though O2 was 90% as my chest was clear and I had no cough. A fortnight later I was able to get an appointment with a different GP who sent me for a chest X ray which showed I had pulmonary fibrosis.
DaveLister
in
Lung Conditions Community Forum
9 months ago
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