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Cinchocaine / Prednisolone hexanoate
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Best way to take Prednisolone
Have different brand of Prednisolone this week so read the information leaflet and it says to dissolve the tablets in large glass of water and wondered if that is a better way to take them ? Previous brand just said take as directed by docter but as there was no instruction I’ve just been swallowing
Have different brand of Prednisolone this week so read the information leaflet and it says to dissolve the tablets in large glass of water and wondered if that is a better way to take them ? Previous brand just said take as directed by docter but as there was no instruction I’ve just been swallowing
Body_bonkers
in
PMRGCAuk
1 year ago
prednisolone
Hi, I have quite mild lupus fortunately but recently I have had a lot of stress in my life and am having an awful flare. I do not take any medication. I went to see my rheumatologist who suggested a short course of steroids. Would anyone be able to help me as to whether they work and help with joint
Hi, I have quite mild lupus fortunately but recently I have had a lot of stress in my life and am having an awful flare. I do not take any medication. I went to see my rheumatologist who suggested a short course of steroids. Would anyone be able to help me as to whether they work and help with joint
fifi6
in
LUPUS UK
1 year ago
The search for reasons
Hi I haven't posted anything for ages and on the whole since my hip replacement, infection and second replacement I have been doing well. PMR symptoms minimal, weight lose steady since I stopped taking prednisone health general improving. Always looking for reasons why it happened to me though. I am
Hi I haven't posted anything for ages and on the whole since my hip replacement, infection and second replacement I have been doing well. PMR symptoms minimal, weight lose steady since I stopped taking prednisone health general improving. Always looking for reasons why it happened to me though. I am
Hiibilly
in
PMRGCAuk
1 year ago
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Mycophenolate or Azathioprine ?
Hi friends, Some of you will remember that in February I had an intolerably itchy rash my Rheumy didn’t recognise as being a Lupus rash but was confirmed by Dermy as such. After being on Prednisolone for a total of 7 weeks tapering down by 5 mg per week, my poor innards were screaming. I couldn’t
Hi friends, Some of you will remember that in February I had an intolerably itchy rash my Rheumy didn’t recognise as being a Lupus rash but was confirmed by Dermy as such. After being on Prednisolone for a total of 7 weeks tapering down by 5 mg per week, my poor innards were screaming. I couldn’t
Spotty-ewe
in
LUPUS UK
1 year ago
Tapering Prednisolone and anxiety.
Good morning, I have been taking varying amounts of Prednisolone since last July…20mg at the beginning when experiencing the start of RA. I started on Hydroxychloroquine in November and Methotrexate in January after having flares in those months which coincided with getting Prednisolone to around 3mg
Good morning, I have been taking varying amounts of Prednisolone since last July…20mg at the beginning when experiencing the start of RA. I started on Hydroxychloroquine in November and Methotrexate in January after having flares in those months which coincided with getting Prednisolone to around 3mg
Biker52
in
NRAS
1 year ago
UTI,s
Dropped fron 22.5 prednisone to 20 three days ago and started having bad uti consequences. It must just be a consequence. See if Bactrim antibiotics works. Have you ever heard of this happening?
Dropped fron 22.5 prednisone to 20 three days ago and started having bad uti consequences. It must just be a consequence. See if Bactrim antibiotics works. Have you ever heard of this happening?
Seal49
in
PMRGCAuk
1 year ago
Hip pain
I searched the archives and cannot find much about this. My hips hurt so much at night that I am awake for hours. I understand this is one of the primary symptoms of PMR, which I was diagnosed with 18 most ago. I had hip scans, and doc says the hip structure is fine. I've been tapering from 20 mg prednisone
I searched the archives and cannot find much about this. My hips hurt so much at night that I am awake for hours. I understand this is one of the primary symptoms of PMR, which I was diagnosed with 18 most ago. I had hip scans, and doc says the hip structure is fine. I've been tapering from 20 mg prednisone
Gigi1946
in
PMRGCAuk
1 year ago
PSMA PET and PSA
Hi, my Dad was diagnosed with PC 2 years ago, had Radiation and has been on Lupron, Abiraterone and Prednisone ever since. Recently he had a PSMA PET that reads: “The prostate gland has decreased in size from 6/6/2022, now spanning 3.6 cm in transverse dimension, previously spanning 4.1 cm in transverse
Hi, my Dad was diagnosed with PC 2 years ago, had Radiation and has been on Lupron, Abiraterone and Prednisone ever since. Recently he had a PSMA PET that reads: “The prostate gland has decreased in size from 6/6/2022, now spanning 3.6 cm in transverse dimension, previously spanning 4.1 cm in transverse
Simonapo
in
Advanced Prostate Cancer
1 year ago
Neck and shoulder pain
Good Morning. My journey with Prednisolone, has been a ‘yo-yo’ experience, but eventually reaching zero after two years, although the resulting symptoms suggested that Methotrexate wasn’t the ‘all conquering hero’ of the hour. Good advice and information from fellow members indicated I might be expecting
Good Morning. My journey with Prednisolone, has been a ‘yo-yo’ experience, but eventually reaching zero after two years, although the resulting symptoms suggested that Methotrexate wasn’t the ‘all conquering hero’ of the hour. Good advice and information from fellow members indicated I might be expecting
JaiSea
in
PMRGCAuk
1 year ago
Any success after multiple failed DE transfers?
Just had my 6th DE failed transfer (3 different donors). Had ERA, ALICE and EMMA, scratch, Hysteroscopy (normal). NK cells - raised cytokines. Been on prednisolone and aspirin. Got 1 embroyo left in the freezer. Any advice/ suggestions much appreciated. Starting to lose hope.
Just had my 6th DE failed transfer (3 different donors). Had ERA, ALICE and EMMA, scratch, Hysteroscopy (normal). NK cells - raised cytokines. Been on prednisolone and aspirin. Got 1 embroyo left in the freezer. Any advice/ suggestions much appreciated. Starting to lose hope.
OT88
in
Fertility Network UK
1 year ago
Rescue pack of prednisolone
Why have some surgeries mine included stopped giving rescue packs of Prednisolone?
Why have some surgeries mine included stopped giving rescue packs of Prednisolone?
marbijusamja
in
Asthma Community Forum
1 year ago
On prednisone with 100 degrees fever
Reduced from 22.5 to 20 mg 3 days ago. I started running a fever between 101.8 and 99.3. Wondering if any connection. Do I need to go to gp or Rheumatologist?
Reduced from 22.5 to 20 mg 3 days ago. I started running a fever between 101.8 and 99.3. Wondering if any connection. Do I need to go to gp or Rheumatologist?
Seal49
in
PMRGCAuk
1 year ago
5mg prednisone is working now, body feels like it has adapted to the lower dose
Aches and pains are much subdued. I do think I can keep lowering, but I am a little worried about my hands now. As in maybe the small amount of prednisone is helping down the inflammation there. I have had carpel tunnel symptoms for at least 10 years. Now I know I have some OA in the hands from the xrays
Aches and pains are much subdued. I do think I can keep lowering, but I am a little worried about my hands now. As in maybe the small amount of prednisone is helping down the inflammation there. I have had carpel tunnel symptoms for at least 10 years. Now I know I have some OA in the hands from the xrays
sdowney717
in
PMRGCAuk
1 year ago
Triggers... for GCA
Well 2018 was bad GCA and weight loss and fatigue. Prednisone got me up and weight back Acterma eliminated the prednisone . So for @14 moths I am off of everything.. I found I had mold in my basement and . have not been sick since it was cleaned . (by me) I told my Doctor she said that its
Well 2018 was bad GCA and weight loss and fatigue. Prednisone got me up and weight back Acterma eliminated the prednisone . So for @14 moths I am off of everything.. I found I had mold in my basement and . have not been sick since it was cleaned . (by me) I told my Doctor she said that its
dansGCA
in
PMRGCAuk
1 year ago
Actemra
I was diagnosed with GCA and PMR in 2018 and lost the vision in my right eye. I was on prednisone and methotrexate for over a year, but then I changed rheumatologists my new one recommended at Actemra actpen. I give myself a dose once every 3 weeks and it has been a great alternative to prednisone. My
I was diagnosed with GCA and PMR in 2018 and lost the vision in my right eye. I was on prednisone and methotrexate for over a year, but then I changed rheumatologists my new one recommended at Actemra actpen. I give myself a dose once every 3 weeks and it has been a great alternative to prednisone. My
brenda1207
in
PMRGCAuk
1 year ago
Starting again?
I have PMR diagnosed Jan 2023. My dosage started at 15 mg reducing so far to 12.5mg. Have just been on a holiday & managed to get E.coli quite badly. Was on a drip + lots of medication so (stupidly?) stopped the Prednisolone for 3 days. Have been back on 12.5 mg as usual so far, but with red face, which
I have PMR diagnosed Jan 2023. My dosage started at 15 mg reducing so far to 12.5mg. Have just been on a holiday & managed to get E.coli quite badly. Was on a drip + lots of medication so (stupidly?) stopped the Prednisolone for 3 days. Have been back on 12.5 mg as usual so far, but with red face, which
Claremont2023
in
PMRGCAuk
1 year ago
Edema post transplant
So one year post transplant and what a complete shitshow.It has been nothing but one thing after another.First got covid from hospital when transplanted,then when being treated in hospital for that picked up COP and had 2 weeks in isolation on iv antibiotics 3 times daily.Finally got home suffer horrible
So one year post transplant and what a complete shitshow.It has been nothing but one thing after another.First got covid from hospital when transplanted,then when being treated in hospital for that picked up COP and had 2 weeks in isolation on iv antibiotics 3 times daily.Finally got home suffer horrible
Parkerbarker
in
Kidney Transplant
1 year ago
have you been treated for osteoporosis?
As predicted following several years on prednisone, my most recent DEXA shows that I now have osteoporosis. There appear to be a variety of treatment options - different meds and different administrations (oral, injection) - which I will discuss with my nephrologist. If you are being treated for osteoporosis
As predicted following several years on prednisone, my most recent DEXA shows that I now have osteoporosis. There appear to be a variety of treatment options - different meds and different administrations (oral, injection) - which I will discuss with my nephrologist. If you are being treated for osteoporosis
Transplant2018
in
Kidney Transplant
1 year ago
Biphosphonates Questions
I’m on my second go-around for GCA. I had GCA/PMR in 2017. After almost 5 years and tapering VERY slowly got off of prednisone for about year when the GCA came back suddenly, but without PMR. Currently at 2mg prednisone from 60 , and Actemra every other week. Just tapered to 2 mg quickly (one
I’m on my second go-around for GCA. I had GCA/PMR in 2017. After almost 5 years and tapering VERY slowly got off of prednisone for about year when the GCA came back suddenly, but without PMR. Currently at 2mg prednisone from 60 , and Actemra every other week. Just tapered to 2 mg quickly (one
Pamk1949
in
PMRGCAuk
1 year ago
GCA, Pred tapering and shoulder pain
I was diagnosed with GCA in April 2022 and have been up and down on Pred. Early last month I dropped from 10mg down to 9mg and since then I have had really bad pain in both my shoulders, back and knees. I’m waking up in the early hours in pain and am so stiff. I’m also getting hot sweats and have
I was diagnosed with GCA in April 2022 and have been up and down on Pred. Early last month I dropped from 10mg down to 9mg and since then I have had really bad pain in both my shoulders, back and knees. I’m waking up in the early hours in pain and am so stiff. I’m also getting hot sweats and have
Hazeleyes48
in
PMRGCAuk
1 year ago
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