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Cinchocaine / Prednisolone hexanoate
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Doctors orders to reduce prednisolone.
Hello folks , I haven’t posted for a while . Have read and checked in though almost daily . Have not been feeling to good of late , can’t seem to get my pain under control . I have a lovely Doc that has seeing me/ or phoning me . She tried to get me a rheumatologist appointment , they said they
Hello folks , I haven’t posted for a while . Have read and checked in though almost daily . Have not been feeling to good of late , can’t seem to get my pain under control . I have a lovely Doc that has seeing me/ or phoning me . She tried to get me a rheumatologist appointment , they said they
Staffieblue
in
PMRGCAuk
1 year ago
omalizumab
Hi, has anyone tried the above injections. I have been approved for this as I have allergic asthma and EILO. I'm currently permanently on Prednisone as inhalers do not work for me and hoping with these injections to be able at some point come off Prednisone. Any feedback would be greatly appreciated
Hi, has anyone tried the above injections. I have been approved for this as I have allergic asthma and EILO. I'm currently permanently on Prednisone as inhalers do not work for me and hoping with these injections to be able at some point come off Prednisone. Any feedback would be greatly appreciated
Loveducks
in
Asthma Community Forum
11 months ago
A different consultant :)
Hello! So, after my last consultant discharged me only for me to go and have a big flare-up immediately afterwards, I managed to get a second opinion appointment with a different consultant. By complete contrast, this one was fantastic - she has referred me to a respiratory physiotherapist and for
Hello! So, after my last consultant discharged me only for me to go and have a big flare-up immediately afterwards, I managed to get a second opinion appointment with a different consultant. By complete contrast, this one was fantastic - she has referred me to a respiratory physiotherapist and for
porthos06
in
Asthma Community Forum
1 year ago
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FET 4/23
Hi there, I have been hiding on this forum for a few months now. Planning to transfer two day 5 embryos (1 poor and 1 fair) at the end of the month. I have a large posterior subserosal fibroid but hysteroscopy was normal so didn’t require a myomectomy. Had a mock embryo transfer last month which was
Hi there, I have been hiding on this forum for a few months now. Planning to transfer two day 5 embryos (1 poor and 1 fair) at the end of the month. I have a large posterior subserosal fibroid but hysteroscopy was normal so didn’t require a myomectomy. Had a mock embryo transfer last month which was
Hidden
in
Fertility Network UK
1 year ago
2 years into Stage 4 Treatment
Hello all, I’m writing for some help regarding my dad. 2 years ago he was diagnosed prostate adenocarcinoma Gleason 5+4 with PSA 146 and Mets to ischium, sacrum and one rib. He started on Zytiga, Lupron and Prednisone and received 20 treatments of radiation to a cumulative dose of 60 Gy. Overall
Hello all, I’m writing for some help regarding my dad. 2 years ago he was diagnosed prostate adenocarcinoma Gleason 5+4 with PSA 146 and Mets to ischium, sacrum and one rib. He started on Zytiga, Lupron and Prednisone and received 20 treatments of radiation to a cumulative dose of 60 Gy. Overall
petdoc
in
Advanced Prostate Cancer
11 months ago
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
Aching and sore hands and feet
I've had PMR and GCA since 2018. I'm now at 3.5 mg prednisone. I've developed carpal tunnel - took up knitting and probably surf on my phone too much! Both my feet and hands and wrists are sore and aching. Carpal tunnel explains the hands and wrists, but what about my feet? I have a new rheumy
I've had PMR and GCA since 2018. I'm now at 3.5 mg prednisone. I've developed carpal tunnel - took up knitting and probably surf on my phone too much! Both my feet and hands and wrists are sore and aching. Carpal tunnel explains the hands and wrists, but what about my feet? I have a new rheumy
Viola1
in
PMRGCAuk
11 months ago
Newly Transplanted Kidney
After three years on the wait list, I got the call last week to come in and have a kidney transplanted from a deceased donor. My expectation that it would be another three years of waiting, so this was quite a pleasant surprise. My whole life changed in an instant. I was so happy and yet very scared
After three years on the wait list, I got the call last week to come in and have a kidney transplanted from a deceased donor. My expectation that it would be another three years of waiting, so this was quite a pleasant surprise. My whole life changed in an instant. I was so happy and yet very scared
Hidden
in
Kidney Transplant
11 months ago
Methotrexate Update
I was prescribed MTX a year ago, about 18months into my PMR journey, I reluctantly followed my Rheumatologist’s instructions and in October reported back to him with details of nausea, 3 days a week of pain, inertia and depression and a prednisone journey of 1mg reduction per month. I asked if I could
I was prescribed MTX a year ago, about 18months into my PMR journey, I reluctantly followed my Rheumatologist’s instructions and in October reported back to him with details of nausea, 3 days a week of pain, inertia and depression and a prednisone journey of 1mg reduction per month. I asked if I could
suelm
in
PMRGCAuk
11 months ago
Night time prednisone
In the US, I have been taking prednisone at night...trying for 2 AM as suggested, but finding insomnia of sorts. Recently taken at 1 AM, but even this which works fine, causes me to awake around 11:30 PM and I try to make it to 2 AM, but struggle and end up taking my 20 mg between 12-1 AM.... I know
In the US, I have been taking prednisone at night...trying for 2 AM as suggested, but finding insomnia of sorts. Recently taken at 1 AM, but even this which works fine, causes me to awake around 11:30 PM and I try to make it to 2 AM, but struggle and end up taking my 20 mg between 12-1 AM.... I know
Joseph14612
in
PMRGCAuk
11 months ago
PMR or Fibromyalgia?
I have been told by drs that I have both PMR and FM. I am tapering my prednisone but am having a hard time determining if I have a FM or PMR flare. Do any of you have both and, if so, how do you know which is which? Thank you in advance!
I have been told by drs that I have both PMR and FM. I am tapering my prednisone but am having a hard time determining if I have a FM or PMR flare. Do any of you have both and, if so, how do you know which is which? Thank you in advance!
emmamom
in
PMRGCAuk
11 months 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
Hand cramp
I'm on prednisone since mid April and so far have been able go from 30 mg to 22.5mg a day Body feels fine but getting cramps only on my right hand which I use alot. Is this a pmr or prednisone side affect or could I have some sort of arthritis also
I'm on prednisone since mid April and so far have been able go from 30 mg to 22.5mg a day Body feels fine but getting cramps only on my right hand which I use alot. Is this a pmr or prednisone side affect or could I have some sort of arthritis also
Seal49
in
PMRGCAuk
11 months ago
MS or PMR or both
I've joined this community to run my symptoms by you. For weeks now I've been having excruciating pain with back muscles spasming. The spasms go from hip girdle all the way up to mid back range. It's like a boa constrictor is wrapped around me and as the days go by, they get even tighter (like this morning
I've joined this community to run my symptoms by you. For weeks now I've been having excruciating pain with back muscles spasming. The spasms go from hip girdle all the way up to mid back range. It's like a boa constrictor is wrapped around me and as the days go by, they get even tighter (like this morning
Missus835
in
My MSAA Community
11 months 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
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
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
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