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Experiences with
Cinchocaine / Prednisolone hexanoate
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Boron
Hello and sympathies to my fellow sufferers . You are all very knowledgeable about RA which is why I am seeking your experienced help regarding Boron. I have been in what I thought was a flare for over two years in spite of Sulfasalazine and regular checks with my Consultant Rheumy. I have had three
Hello and sympathies to my fellow sufferers . You are all very knowledgeable about RA which is why I am seeking your experienced help regarding Boron. I have been in what I thought was a flare for over two years in spite of Sulfasalazine and regular checks with my Consultant Rheumy. I have had three
tangolil
in
NRAS
1 year ago
Stable PSA, deep fall testosterone lab results.
At this point I am only getting Lupron injections every four months. Zytiga and Prednisone stopped two months ago. PSA un changed at 1.06 for the last 4 months, testosterone down from 100 last month to 17 yesterday. Kindly asking, what will be the point of starting on Xtandi and get exposed to its nasty
At this point I am only getting Lupron injections every four months. Zytiga and Prednisone stopped two months ago. PSA un changed at 1.06 for the last 4 months, testosterone down from 100 last month to 17 yesterday. Kindly asking, what will be the point of starting on Xtandi and get exposed to its nasty
Blueribbon63
in
Advanced Prostate Cancer
1 year ago
Allegra for asthma?
I have recently moved from the UK to Germany/Switzerland; the halthcare is in Germany. Getting Xolair, anti-IL5 mAbs, prednisone, inhalers and other drugs was super-easy. But I still get very chest-tight due to the high pollen counts. I believe here the pollen-triggered asthma is worse, b.c. of the warmer
I have recently moved from the UK to Germany/Switzerland; the halthcare is in Germany. Getting Xolair, anti-IL5 mAbs, prednisone, inhalers and other drugs was super-easy. But I still get very chest-tight due to the high pollen counts. I believe here the pollen-triggered asthma is worse, b.c. of the warmer
runcyclexcski
in
Asthma Community Forum
1 year ago
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DSNS tapering
hi I have been trying for over a year to get below 7 mg of prednisone Decided to try the DSNS method I am now at 6,5 new and 2. Days of old 7 mg When I take the new dose the next day I get severe migraines and stomach cramps and from the start of tapering I have lost 4 lbs which I can’t affor at
hi I have been trying for over a year to get below 7 mg of prednisone Decided to try the DSNS method I am now at 6,5 new and 2. Days of old 7 mg When I take the new dose the next day I get severe migraines and stomach cramps and from the start of tapering I have lost 4 lbs which I can’t affor at
tulazik3001
in
PMRGCAuk
1 year ago
Help please, Getting flare under control
I was trending quite well, down to 2.5mgs. Caught Covid two months and was put on antivirals and managed to escape any unwanted side effects of the virus. Unfortunately I started to experience symptoms of a flare of PMR. I increased my dose to 4mgs , then 4.5 and now 5mgs. It hasn’t made any difference
I was trending quite well, down to 2.5mgs. Caught Covid two months and was put on antivirals and managed to escape any unwanted side effects of the virus. Unfortunately I started to experience symptoms of a flare of PMR. I increased my dose to 4mgs , then 4.5 and now 5mgs. It hasn’t made any difference
golfnutter
in
PMRGCAuk
1 year ago
NOT PMR, says the Rheumy, after almost 7 years! YOU WHAT?
Have I just had an appointment with the worst NHS Rheumatologist out there or has he got it right? It’s probably never been PMR, says he, just arthritis! Your CRP is 1. It certainly isn’t extra cranial GCA as there is no claudication on chewing or speaking. He felt round my jaw, expecting TMJ which
Have I just had an appointment with the worst NHS Rheumatologist out there or has he got it right? It’s probably never been PMR, says he, just arthritis! Your CRP is 1. It certainly isn’t extra cranial GCA as there is no claudication on chewing or speaking. He felt round my jaw, expecting TMJ which
Zebedee44
in
PMRGCAuk
1 year ago
Mannitol challenge
Hi, hope you are all well. 😊 Bit of a long story sorry…. I’ve recently seen a new consultant, who is sending me for a ‘mannitol’ challenge test and wondered if anyone else who has similar asthma to me, has had experience of this and what the outcome was. A consultant I saw a couple of years ago,
Hi, hope you are all well. 😊 Bit of a long story sorry…. I’ve recently seen a new consultant, who is sending me for a ‘mannitol’ challenge test and wondered if anyone else who has similar asthma to me, has had experience of this and what the outcome was. A consultant I saw a couple of years ago,
Celie1
in
Asthma Community Forum
1 year ago
TB testing before starting a biologic.
Hi everyone, hope your all well as can be.I'm to start a biologic soon, so had my bloods done, (microbiology) bloods for TB has come back positive, I've been referred to a respiratory specialist for further testing. I'm not doing very well at all at the moment, im in a massive flaire, and currently
Hi everyone, hope your all well as can be.I'm to start a biologic soon, so had my bloods done, (microbiology) bloods for TB has come back positive, I've been referred to a respiratory specialist for further testing. I'm not doing very well at all at the moment, im in a massive flaire, and currently
jojoishere
in
NRAS
1 year ago
Advice about plan of treatment
I am 67, was diagnosed with PMR 2 weeks ago after 4 weeks of symptoms (stiffness and pain in neck, arms, shoulders, couldn't raise arms above shoulders, immense tiredness etc). Initial GP contact was excellent - he identified the problem, blood tests same day, consult 2 days later to confirm diagnosis
I am 67, was diagnosed with PMR 2 weeks ago after 4 weeks of symptoms (stiffness and pain in neck, arms, shoulders, couldn't raise arms above shoulders, immense tiredness etc). Initial GP contact was excellent - he identified the problem, blood tests same day, consult 2 days later to confirm diagnosis
MarionA
in
PMRGCAuk
1 year ago
Fuzzy head and top of head pressure that comes and goes???
HiI am currently taking 7.5 mg am and 0.75 pm of prednisone and been at this level for a few weeks. During the past week I have had episodes of fuzzy head and pressure/tightness on the top of my head. These come and go during the day for no reason that I know of. Any one have any insights as to what
HiI am currently taking 7.5 mg am and 0.75 pm of prednisone and been at this level for a few weeks. During the past week I have had episodes of fuzzy head and pressure/tightness on the top of my head. These come and go during the day for no reason that I know of. Any one have any insights as to what
dccarver
in
PMRGCAuk
1 year ago
More from PubMed
1. Magnetic resonance imaging (MRI) for local staging before salvage radical prostatectomy: a meta-analysis. Zapała P, Ślusarczyk A, Rajwa P, Gandaglia G, Zapała Ł, Zattoni F, Lorenc T, Ploussard G, Radziszewski P. World J Urol. 2023 May;41(5):1275-1284. doi: 10.1007/s00345-023-04383-2. Epub 2023 Apr
1. Magnetic resonance imaging (MRI) for local staging before salvage radical prostatectomy: a meta-analysis. Zapała P, Ślusarczyk A, Rajwa P, Gandaglia G, Zapała Ł, Zattoni F, Lorenc T, Ploussard G, Radziszewski P. World J Urol. 2023 May;41(5):1275-1284. doi: 10.1007/s00345-023-04383-2. Epub 2023 Apr
Magnus1964
in
Advanced Prostate Cancer
1 year ago
RA pain & inflammation causing terrible anxiety: pacing, insomnia
Experiencing terrible anxiety & insomnia when RA pain flares up- but gp & rheum won’t give sedatives. They act like I’m an addict; so I take a few glasses of wine & I don’t even like liquor. Am in the USA. These drs have no problem giving expensive, “big gun” RA meds & high dose prednisone - but
Experiencing terrible anxiety & insomnia when RA pain flares up- but gp & rheum won’t give sedatives. They act like I’m an addict; so I take a few glasses of wine & I don’t even like liquor. Am in the USA. These drs have no problem giving expensive, “big gun” RA meds & high dose prednisone - but
Hisue
in
NRAS
1 year ago
The Double Vision Issue with GCA
Hi all, I'm a GCA patient, having been diagnosed in AUG 2022. I started on 60 MG PRED, and after 9 months have titrated down to 12.5MG. I am under the care of a GP, ophthalmologist, and rheumatologist. PRIOR to being diagnosed with GCA, somewhere around MARCH 2022, I started noticing I had double
Hi all, I'm a GCA patient, having been diagnosed in AUG 2022. I started on 60 MG PRED, and after 9 months have titrated down to 12.5MG. I am under the care of a GP, ophthalmologist, and rheumatologist. PRIOR to being diagnosed with GCA, somewhere around MARCH 2022, I started noticing I had double
montebello
in
PMRGCAuk
1 year ago
Newbie to the group.
Hi all, I’m new to the group although 6 months in on a PMR diagnosis. My symptoms started in April 2020 2 months after as knee injury, both my shoulders at first, I couldn’t even get a cup off the side, couldn’t lay on my side or touch my shoulders. I thought that it was over use. My GP prescribed
Hi all, I’m new to the group although 6 months in on a PMR diagnosis. My symptoms started in April 2020 2 months after as knee injury, both my shoulders at first, I couldn’t even get a cup off the side, couldn’t lay on my side or touch my shoulders. I thought that it was over use. My GP prescribed
Binnie49
in
PMRGCAuk
1 year ago
question regarding otc pain relief
I am currently on daily zytiga plus prednisone and monthly firmagon. . I have mostly avoided any pain meds. Recently, I overexerted while doing yard work and hurt the lower back. We now are hiking in the Finger Lakes and rest on the back isn’t as practical, but the back isn’t cooperating. Tylenol
I am currently on daily zytiga plus prednisone and monthly firmagon. . I have mostly avoided any pain meds. Recently, I overexerted while doing yard work and hurt the lower back. We now are hiking in the Finger Lakes and rest on the back isn’t as practical, but the back isn’t cooperating. Tylenol
Gatodd
in
Advanced Prostate Cancer
1 year ago
Spring Covid booster - no longer on the list
Hi all, I wonder if anyone else has had this experience. I've always been on the CEV list and eligible for boosters. However, my GP surgery are telling me I am not eligible this time round. I have Lupus/APS and take prednisolone. On both counts I seem to qualify on the grounds of having a weakened
Hi all, I wonder if anyone else has had this experience. I've always been on the CEV list and eligible for boosters. However, my GP surgery are telling me I am not eligible this time round. I have Lupus/APS and take prednisolone. On both counts I seem to qualify on the grounds of having a weakened
Treetop33
in
LUPUS UK
1 year ago
Which is the worst - Prednisolone or Methatrexate?
I’ve mentioned my position in reply to other’s posts, but briefly, Jan 2023 - having been convinced the MTX wasn’t making any difference, I asked to stop it but my Rheumy said no, but you can half your dose to 10mg (once a week). I was also on 1.5mg Pred with Rhuemy pushing me to reduce by .5 for
I’ve mentioned my position in reply to other’s posts, but briefly, Jan 2023 - having been convinced the MTX wasn’t making any difference, I asked to stop it but my Rheumy said no, but you can half your dose to 10mg (once a week). I was also on 1.5mg Pred with Rhuemy pushing me to reduce by .5 for
Prof99
in
PMRGCAuk
1 year ago
Two years after diagnosis
Just wanted to say hello and thanks to all for the information on here which I have found encouraging and helpful. I am 66, male and was diagnosed with PMR two years ago after the pain became so bad that I finally got in touch with my GP. I am now down to two mg of Prednisolone after a bit of a struggle
Just wanted to say hello and thanks to all for the information on here which I have found encouraging and helpful. I am 66, male and was diagnosed with PMR two years ago after the pain became so bad that I finally got in touch with my GP. I am now down to two mg of Prednisolone after a bit of a struggle
Colin-s
in
PMRGCAuk
1 year ago
Is it Fibromyalgia?
I was diagnosed with PMR in January 2021 and started taking Prednisolone. The following November I fractured my humerus and while I was recovering began to experience pain in my lower back and legs to the extent that walking was very painful. I had an X-ray of my lumbar region which showed degenerative
I was diagnosed with PMR in January 2021 and started taking Prednisolone. The following November I fractured my humerus and while I was recovering began to experience pain in my lower back and legs to the extent that walking was very painful. I had an X-ray of my lumbar region which showed degenerative
Jomaur
in
Fibromyalgia Action UK
1 year ago
Changing from prednisone to Midazolam
from approx 1973 until 2015 I had very mild asthma. Come Feb 2015 following a major neck operation it started getting worse. approx April 2015 the respiratory clinic thought I may have copd. This was confirmed later that year. My asthma is now classed as severe along with the COPD. I also have Restless
from approx 1973 until 2015 I had very mild asthma. Come Feb 2015 following a major neck operation it started getting worse. approx April 2015 the respiratory clinic thought I may have copd. This was confirmed later that year. My asthma is now classed as severe along with the COPD. I also have Restless
Bevash
in
Asthma Community Forum
1 year ago
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