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Experiences with
Cinchocaine / Prednisolone hexanoate
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How to cope with workload
I was diagnosed with atypical PMR two and half years back. Being ill has disrupted my worklife seriously but I as I do freelance work from home I have sort of managed. Having reasonable deadlines has been crucial for my coping strategy. However I have just gotten a rather big assigment that needs to
I was diagnosed with atypical PMR two and half years back. Being ill has disrupted my worklife seriously but I as I do freelance work from home I have sort of managed. Having reasonable deadlines has been crucial for my coping strategy. However I have just gotten a rather big assigment that needs to
Quintius
in
PMRGCAuk
1 month ago
Merry Christmas,Happy New Year with thanks
It will be 4yrs this coming January for me with PMR. Down to 2.5 mg Prednisolone 4 days and 5mg 3 days a week. iI would just like to say many thanks to those that run this forum and to those who contribute such helpful information and advice. You are all wonderful. đź‘Źxxxx
It will be 4yrs this coming January for me with PMR. Down to 2.5 mg Prednisolone 4 days and 5mg 3 days a week. iI would just like to say many thanks to those that run this forum and to those who contribute such helpful information and advice. You are all wonderful. đź‘Źxxxx
Sandyowl
in
PMRGCAuk
7 months ago
New person here...
My first post here... I'm a hotbed of autoimmune disorders: arthritis, PMR, Hashimoto's Thyroiditis, & Sjegren's. I've been dealing with pain most of my life (I'm 79) but was only recently (officially) diagnosed with PMR. In the meantime, over the past 53 years I was told my pain was caused by a
My first post here... I'm a hotbed of autoimmune disorders: arthritis, PMR, Hashimoto's Thyroiditis, & Sjegren's. I've been dealing with pain most of my life (I'm 79) but was only recently (officially) diagnosed with PMR. In the meantime, over the past 53 years I was told my pain was caused by a
79andCounting
in
PMRGCAuk
1 month ago
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Bad reaction to Prednisone?
Hello all Has any one had a very quick unpleasant reaction to taking Prednisone tablets. I have taken 10mg yesterday and 5mg today. I started feeling very woozy, lightheaded, as if I am drunk since lunchtime. I had Prednisone a few years back when I was put on about 40mg tablets, I had to come off
Hello all Has any one had a very quick unpleasant reaction to taking Prednisone tablets. I have taken 10mg yesterday and 5mg today. I started feeling very woozy, lightheaded, as if I am drunk since lunchtime. I had Prednisone a few years back when I was put on about 40mg tablets, I had to come off
Mouseling
in
NRAS
1 month ago
Side Effects
Has anybody had Oral Thrush side effect of Prednisone ? And how do you get rid of it without going to to the Drs for more medication. Thank you
Has anybody had Oral Thrush side effect of Prednisone ? And how do you get rid of it without going to to the Drs for more medication. Thank you
budgies4
in
PMRGCAuk
1 month ago
does anyone know if it’s safe to take 300-600 mg of Gabapentin while taking 600 mg of horizant and 2 mg of pramipexole?
details: I was taking 3-4 mg of pramipexole for my RLs. Developed augmentation. Sleep dr put me on 600 mg of horizant and supposed to taper the pram. I’m at 2 mg of pram. Today went to ortho for a back issue and waiting on mri appt. In the meantime ortho prescribed 300-600 mg of Gabapentin for the pain
details: I was taking 3-4 mg of pramipexole for my RLs. Developed augmentation. Sleep dr put me on 600 mg of horizant and supposed to taper the pram. I’m at 2 mg of pram. Today went to ortho for a back issue and waiting on mri appt. In the meantime ortho prescribed 300-600 mg of Gabapentin for the pain
BluGenie
in
Restless Legs Syndrome
1 month ago
PET CT Scan
I have had PMR since Feb 23 and had a PET CT scan today. Has anyone else had one of these? what was the outcome my blood markers have been high during the whole time, I have tapered prednisone from 15 mg to 4.5mg.
I have had PMR since Feb 23 and had a PET CT scan today. Has anyone else had one of these? what was the outcome my blood markers have been high during the whole time, I have tapered prednisone from 15 mg to 4.5mg.
pmrdays
in
PMRGCAuk
1 month ago
GCA and Elevation
I have had PMR for 5 years and was diagnosed with GCA in September of 2023. I presently am on 4mg of prednisone. I am feeling good and continue to be pretty active and just turned 70 year old. I walk at least 3 miles a day, bike long distances and kayak. I plan on taking a hike up to 10,000 feet
I have had PMR for 5 years and was diagnosed with GCA in September of 2023. I presently am on 4mg of prednisone. I am feeling good and continue to be pretty active and just turned 70 year old. I walk at least 3 miles a day, bike long distances and kayak. I plan on taking a hike up to 10,000 feet
Mooreby
in
PMRGCAuk
1 month ago
Pacing Activity with GCA
I was diagnosed with GCA in April 2024 and am currently on 40 mg of prednisone and methotrexate. I have not felt “normal” by any means but recently I was able to do a bit more even with my heavy legs/arms and fatigue. However, I may have overdone it for a few days and the fatigue has increased, scalp
I was diagnosed with GCA in April 2024 and am currently on 40 mg of prednisone and methotrexate. I have not felt “normal” by any means but recently I was able to do a bit more even with my heavy legs/arms and fatigue. However, I may have overdone it for a few days and the fatigue has increased, scalp
Moaningxcat
in
PMRGCAuk
1 month ago
pectoralis major discomfort ??
Hi, For a few months before I was diagnosed with PMR I had discomfort across my upper chest. I attributed it to everything from poor posture to muscle strain even though I felt I had done nothing to aggravate it. It lasted several months , went to a physio thinking it would help and I did the recommended
Hi, For a few months before I was diagnosed with PMR I had discomfort across my upper chest. I attributed it to everything from poor posture to muscle strain even though I felt I had done nothing to aggravate it. It lasted several months , went to a physio thinking it would help and I did the recommended
Fishtacoqueen
in
PMRGCAuk
1 month ago
Covid
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
JLAR01
in
LUPUS UK
7 months ago
Off Prednisone for 3 weeks but.......
I have been on prednisone since May of 2021. 10 months ago my rheumatologist added Actemra infusions to my regimen. 3 weeks ago I finally was completely weaned off of prednisone. This past week, and just one day after my infusion, I started having severe stomach cramping, diarrhea, shoulder joint pains
I have been on prednisone since May of 2021. 10 months ago my rheumatologist added Actemra infusions to my regimen. 3 weeks ago I finally was completely weaned off of prednisone. This past week, and just one day after my infusion, I started having severe stomach cramping, diarrhea, shoulder joint pains
A77bruin
in
PMRGCAuk
2 months ago
With humility and respect, some PMR lessons learned
Hello everyone, After about five years with PMR and following a very slow taper regime, I have been off prednisone since January, and I have had no recurrences. I have appreciated the contributions of this site so much. In return, with respect and humility, I report my own observations below in the
Hello everyone, After about five years with PMR and following a very slow taper regime, I have been off prednisone since January, and I have had no recurrences. I have appreciated the contributions of this site so much. In return, with respect and humility, I report my own observations below in the
Marinescience
in
PMRGCAuk
2 months ago
it’s not all asthma
I have only been officially asthmatic since 2017. I was diagnosed with cough variant asthma During that time I have had many courses of prednisolone and had a PPI added for acid reflux. This medication has been increased and my asthma medication added to and changed. In October I saw a locum GP as
I have only been officially asthmatic since 2017. I was diagnosed with cough variant asthma During that time I have had many courses of prednisolone and had a PPI added for acid reflux. This medication has been increased and my asthma medication added to and changed. In October I saw a locum GP as
Oldandgray
in
Asthma Community Forum
7 months ago
cluster headaches
Hi I’ve been suffering for weeks with what I now know are cluster headaches. I’m in agony, I tried a treatment yesterday that you use up your nostril but you only got one dose so 4am this morning it’s back with a vengeance. The only thing I can think that started this was starting prednisone. Has anyone
Hi I’ve been suffering for weeks with what I now know are cluster headaches. I’m in agony, I tried a treatment yesterday that you use up your nostril but you only got one dose so 4am this morning it’s back with a vengeance. The only thing I can think that started this was starting prednisone. Has anyone
Numptybrain
in
National Migraine Centre
2 months ago
Tiredness from Zytiga
Hi group! My Dad who is 89 started Zytiga 3 weeks ago for advanced prostate cancer with mets to bone. He takes the Zytiga at 9:30 am with the prednisone on an empty stomach and has 1 Lupron injection. He is unable to wake up until late afternoon and is always tired and we were wondering if the Zytiga
Hi group! My Dad who is 89 started Zytiga 3 weeks ago for advanced prostate cancer with mets to bone. He takes the Zytiga at 9:30 am with the prednisone on an empty stomach and has 1 Lupron injection. He is unable to wake up until late afternoon and is always tired and we were wondering if the Zytiga
KatRobin71
in
Advanced Prostate Cancer
2 months ago
apalutamide vs. abiraterone
My husband has been recommended ADT + abiraterone + prednisone for two years. My friend who is an oncologist suggested apalutamide instead as it doesn't need to be supplements with prednisone and has less side effects. Wanted your opinion.
My husband has been recommended ADT + abiraterone + prednisone for two years. My friend who is an oncologist suggested apalutamide instead as it doesn't need to be supplements with prednisone and has less side effects. Wanted your opinion.
SherryKahn
in
Advanced Prostate Cancer
2 months ago
Reducing Effects
I just read DL’s very helpful article, Reducing Steroids & Activating the Adrenal Glands. So grateful for all the information and support here. It would’ve felt like walking through a dark and threatening forest without you all. I guess I’m reaching out for the usual reassurance and encouragement regarding
I just read DL’s very helpful article, Reducing Steroids & Activating the Adrenal Glands. So grateful for all the information and support here. It would’ve felt like walking through a dark and threatening forest without you all. I guess I’m reaching out for the usual reassurance and encouragement regarding
Lenore58
in
PMRGCAuk
2 months ago
Prolia and prednisone together = higher infection risk
https://www.drugs.com/drug-interactions/prednisone-with-prolia-1936-0-3238-14600.html From the "we never stop learning angles about APCa and related treatments" zone Wear a mask etc
https://www.drugs.com/drug-interactions/prednisone-with-prolia-1936-0-3238-14600.html From the "we never stop learning angles about APCa and related treatments" zone Wear a mask etc
Derf4223
in
Advanced Prostate Cancer
2 months ago
decrease in Pred after hospital admission
I had been admitted via A&E to hospital with a small rupture to the large intestine and diverticulitis flare, it was a rough time and on lots of meds to correct-was in hospital for 10 days. I am now back home under the care of GP. Whilst in hospital one of the meds, and I was on an enormous amounts
I had been admitted via A&E to hospital with a small rupture to the large intestine and diverticulitis flare, it was a rough time and on lots of meds to correct-was in hospital for 10 days. I am now back home under the care of GP. Whilst in hospital one of the meds, and I was on an enormous amounts
Crwbin1
in
PMRGCAuk
2 months ago
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