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How much prednisone should you take for adrenal fatigue?
I have seen many posts here by patients treated by Dr. P in the UK and who were told to take either prednisone or Nutri Adrenals Extra or both for the rest of their lives. From the posts I´ve read, it would seem they were prescribed a full replacement dose of pred (5 mg or more daily). I consulted a
I have seen many posts here by patients treated by Dr. P in the UK and who were told to take either prednisone or Nutri Adrenals Extra or both for the rest of their lives. From the posts I´ve read, it would seem they were prescribed a full replacement dose of pred (5 mg or more daily). I consulted a
Hidden
in
Thyroid UK
4 years ago
Should You Get the COVID-19 Vaccine If You Have a History of Allergic Reactions to Infused or Injectable Medications?
Here’s what you need to know about the current guidance and potential risks of getting a COVID-19 vaccine if you’ve had allergic reactions to infused or injectable medication. Learn more about our FREE COVID-19 Patient Support Program for chronic illness patients and their loved ones. Biologic Infusions
Here’s what you need to know about the current guidance and potential risks of getting a COVID-19 vaccine if you’ve had allergic reactions to infused or injectable medication. Learn more about our FREE COVID-19 Patient Support Program for chronic illness patients and their loved ones. Biologic Infusions
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
3 years ago
Confused newbie...
August 2019, I suddenly with diffuse body pain (the most excruciating located at the base of my thumbs). I was transported to the ER. 3 times in 6 days, was treated with strong steroids (had a horrid reaction to 7 days of Dexamethazone), and simply continued with Diclofenac until February 2020. Was
August 2019, I suddenly with diffuse body pain (the most excruciating located at the base of my thumbs). I was transported to the ER. 3 times in 6 days, was treated with strong steroids (had a horrid reaction to 7 days of Dexamethazone), and simply continued with Diclofenac until February 2020. Was
CO_mtnLady
in
PMRGCAuk
4 years ago
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Shielding Query
Does whether you’re advised to shield or not depend on your RA diagnosis or the medications you take for it? I’m asking because I had a letter originally, then a letter telling me to ignore the first letter. I had to stop taking the usual DMARDS due to intolerances which just left me with my IM Depo-Medrone
Does whether you’re advised to shield or not depend on your RA diagnosis or the medications you take for it? I’m asking because I had a letter originally, then a letter telling me to ignore the first letter. I had to stop taking the usual DMARDS due to intolerances which just left me with my IM Depo-Medrone
Blackwitch
in
NRAS
4 years ago
My Neuro Appt.
Was yesterday morning.. good thing to, cause I lost power for for close to 4 hrs.😒 My muscles in my back and neck have been so tight. That I actually liked those WWF wrestlers 😭 and it hurt, OMG it hurt! All because of the steroids. So 1st thing on the chopping block... NO MORE!! Prednisone? NOOO
Was yesterday morning.. good thing to, cause I lost power for for close to 4 hrs.😒 My muscles in my back and neck have been so tight. That I actually liked those WWF wrestlers 😭 and it hurt, OMG it hurt! All because of the steroids. So 1st thing on the chopping block... NO MORE!! Prednisone? NOOO
Jesmcd2
CommunityAmbassador
in
My MSAA Community
4 years ago
Pred timing
Is it better to take Medrol at nighttime inside the time release capsules or in the morning? I had been taking at nighttime and after watching Dr Sarah Mackie’s recent lecture I have changed it to the morning. But am feeling stiffer and a bit more achy. She states that taking the prednisone in the morning
Is it better to take Medrol at nighttime inside the time release capsules or in the morning? I had been taking at nighttime and after watching Dr Sarah Mackie’s recent lecture I have changed it to the morning. But am feeling stiffer and a bit more achy. She states that taking the prednisone in the morning
kimsaunsc
in
PMRGCAuk
4 years ago
True that!
How are you doing with your MS? 🤔 Mine stinks! Always stinks!🤣 Had Ocruvus on Monday, w/ solumedrol.. the reaction to it, hit me in the middle of Weds. I hurt soooooo bad😭😭 I can hardly turn my neck! I so hate steroids!! Nough bout me! Tell me about you! 🤗💕🌠
How are you doing with your MS? 🤔 Mine stinks! Always stinks!🤣 Had Ocruvus on Monday, w/ solumedrol.. the reaction to it, hit me in the middle of Weds. I hurt soooooo bad😭😭 I can hardly turn my neck! I so hate steroids!! Nough bout me! Tell me about you! 🤗💕🌠
Jesmcd2
CommunityAmbassador
in
My MSAA Community
4 years ago
Late Christmas wishes.
Merry Christmas wishes to my loving MS family. My flare turned into a pretty bad relapse and pretty much put my pt on extremely light duty the last 2 weeks but I’m happy to say my neurologist finally ordered 3 days of solumedrol Wednesday so they got supplies to me Wednesday night and a nurse to the
Merry Christmas wishes to my loving MS family. My flare turned into a pretty bad relapse and pretty much put my pt on extremely light duty the last 2 weeks but I’m happy to say my neurologist finally ordered 3 days of solumedrol Wednesday so they got supplies to me Wednesday night and a nurse to the
Doubled51
in
My MSAA Community
4 years ago
Officially tapering as of today~!
Sometimes I am confused as to whether this is attempt 3 or 4, I think it is 3. In July of 2020 I got down to 8 mg of Medrol but started having blurriness in my right eye so went back up to 16 mg per day. Since November 2020 I've been on 12 Medrol per day along with Actemra. I had mentioned in a post
Sometimes I am confused as to whether this is attempt 3 or 4, I think it is 3. In July of 2020 I got down to 8 mg of Medrol but started having blurriness in my right eye so went back up to 16 mg per day. Since November 2020 I've been on 12 Medrol per day along with Actemra. I had mentioned in a post
Grammy80
in
PMRGCAuk
4 years ago
Vasculitis in my Spine "Central nervous system Vasculitis"
Just about over a massive flare. It came on sudden. Had a terrible migraine for 3 days with pain in my lower back, discomfort in my spine and pain in my legs that felt like growing pains yet I'm an adult. It was there constantly and nagging. Just felt strange. Woke the Sunday morning with not being
Just about over a massive flare. It came on sudden. Had a terrible migraine for 3 days with pain in my lower back, discomfort in my spine and pain in my legs that felt like growing pains yet I'm an adult. It was there constantly and nagging. Just felt strange. Woke the Sunday morning with not being
Zuzu798
in
Behçet's UK
4 years ago
Out of Remission. Starting over...
Hi everyone, Unfortunately after three months of remission I had a very bad flareup. The week before my husband and I were leaving for Maine (Sept) I decided to get a flu shot. Four days later while in Maine I started not to feel well. The usual PMR symptoms. I had no medication with me. My doctor
Hi everyone, Unfortunately after three months of remission I had a very bad flareup. The week before my husband and I were leaving for Maine (Sept) I decided to get a flu shot. Four days later while in Maine I started not to feel well. The usual PMR symptoms. I had no medication with me. My doctor
Marie1479
in
PMRGCAuk
4 years ago
Has anyone else noticed hormone requirement changing once you reach end-stage Hashimoto´s?
I expected to required T3 and T4 at this stage, but not only do I only seem to require T4, but also lower doses now than 20 years ago when I was diagnosed. Back then, an ultrasound showed my thyroid gland was of normal size, but that there was already extensive damage to the hormone-producing cells.
I expected to required T3 and T4 at this stage, but not only do I only seem to require T4, but also lower doses now than 20 years ago when I was diagnosed. Back then, an ultrasound showed my thyroid gland was of normal size, but that there was already extensive damage to the hormone-producing cells.
Hidden
in
Thyroid UK
4 years ago
I paid the doctor....now for your input!
First let me say my laptop is in the shape...I’m not too fast on the Ipad! The rheumatologist told me today that he wants me to stay on Actemra for another month before tapering. AND....he is going to switch me from prednisolone (Been on —solone for 15 months) to prednisone per day for this coming
First let me say my laptop is in the shape...I’m not too fast on the Ipad! The rheumatologist told me today that he wants me to stay on Actemra for another month before tapering. AND....he is going to switch me from prednisolone (Been on —solone for 15 months) to prednisone per day for this coming
Grammy80
in
PMRGCAuk
4 years ago
Taper?- small reductions but is in relapse or withdrawal ?
Dear PMR, Could I ask a question about dosage, tapering and possible relapse. My original symptoms were triggered, I think, a very, very bad chest infection 18 months ago where I was very ill for a month and a half. I appeared to recover, but then and after 8 months, these symptoms came about suddenly
Dear PMR, Could I ask a question about dosage, tapering and possible relapse. My original symptoms were triggered, I think, a very, very bad chest infection 18 months ago where I was very ill for a month and a half. I appeared to recover, but then and after 8 months, these symptoms came about suddenly
Predderman2020
in
PMRGCAuk
4 years ago
Should You Get the COVID-19 Vaccine If You Have a History of Allergic Reactions to Infused or Injectable Medications?
Picture: Covid-19 BMJ Here’s what you need to know about the current guidance and potential risks of getting a COVID-19 vaccine if you’ve had allergic reactions to infused or injectable medication.
Biologic Infusions
Nearly as soon as the mRNA COVID-19 vaccines from Pfizer and Moderna were
Picture: Covid-19 BMJ Here’s what you need to know about the current guidance and potential risks of getting a COVID-19 vaccine if you’ve had allergic reactions to infused or injectable medication.
Biologic Infusions
Nearly as soon as the mRNA COVID-19 vaccines from Pfizer and Moderna were
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
Ocrevus
I started Solu Medrol 1000mg x 3 treatment on yesterday and will complete on 11/13. I’m getting ready to start Ocrevus after I was told Tecfidera is failing after 2 1/2mths, I developed 2 lesion one an active and other nonactive since Last MRI In Feb. As I was told the lesions possible developed during
I started Solu Medrol 1000mg x 3 treatment on yesterday and will complete on 11/13. I’m getting ready to start Ocrevus after I was told Tecfidera is failing after 2 1/2mths, I developed 2 lesion one an active and other nonactive since Last MRI In Feb. As I was told the lesions possible developed during
JSSimp
in
My MSAA Community
4 years ago
Depo-Medrone is done with me, but lasted almost a month
I had the Depo on 13th November and can officially say the positive effects have worn off. It is weird how you can feel the RA gradually taking over again. So back to stiffness and hand/wrist issues and the Metoject doesn't seem to help at all. 17.5ml not doing anything worthwhile and I am about to
I had the Depo on 13th November and can officially say the positive effects have worn off. It is weird how you can feel the RA gradually taking over again. So back to stiffness and hand/wrist issues and the Metoject doesn't seem to help at all. 17.5ml not doing anything worthwhile and I am about to
Brushwork
in
NRAS
4 years ago
TPLL
I want to thank you all again for welcoming me into your community. Mike's cancer diagnosis has been very unique. As has his treatment. I don't recall what I have already shared, but his actual diagnosis ended up being TPLL (Tcell Prolymphocytic Leukemia). His WBC count went from 432,000 on 9/30 to 530,000
I want to thank you all again for welcoming me into your community. Mike's cancer diagnosis has been very unique. As has his treatment. I don't recall what I have already shared, but his actual diagnosis ended up being TPLL (Tcell Prolymphocytic Leukemia). His WBC count went from 432,000 on 9/30 to 530,000
Whatadayitwas
in
CLL Support
4 years ago
So sleepy - since the Depo- steroid jab?
Not complaining. My wrist swelling is down and function is improved though not fully restored, I think there is damage, and morning stiffness and pain is gone (for now), since I had the Depo-Medrone jab. However, I am sleeping about 8 - 10 hrs! My usual is 6-8, so its a bit odd. The Methotrexate makes
Not complaining. My wrist swelling is down and function is improved though not fully restored, I think there is damage, and morning stiffness and pain is gone (for now), since I had the Depo-Medrone jab. However, I am sleeping about 8 - 10 hrs! My usual is 6-8, so its a bit odd. The Methotrexate makes
Brushwork
in
NRAS
4 years ago
Flare clinic - update, still not wearing flares though 😊
Thanks for all the positive support yesterday. It seems that Aberdeen RI, Rheumy dept have decided to re-organise how they see people. In addition to video and telephone consults, they are running 2 flare clinics a month. Good idea. Well organised. Not the doctor the letter indicated but one of my usual
Thanks for all the positive support yesterday. It seems that Aberdeen RI, Rheumy dept have decided to re-organise how they see people. In addition to video and telephone consults, they are running 2 flare clinics a month. Good idea. Well organised. Not the doctor the letter indicated but one of my usual
Brushwork
in
NRAS
4 years ago
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