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Prednisone
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12 days Post Day 5 Embryo Transfer. Grade 4 ab and 2cc. Negative PT. LOOSING FAITH
Under clexane,
prednisone
, cricone, duphastone, estrogen pills. Where do I go from here? I am defeated and tired, I cannot open to anyone they will not understand me especially if you can be pregnant naturally.
Under clexane,
prednisone
, cricone, duphastone, estrogen pills. Where do I go from here? I am defeated and tired, I cannot open to anyone they will not understand me especially if you can be pregnant naturally.
have_faith12
in
Fertility Network UK
8 months ago
Montelukast
I had a very bad chest infection for 6 weeks was on doxycycline 500 for two weeks alongside
prednisone
steroids for 6 weeks I have been put on Montelukast 10mg once a night for 8 weeks been on them 9 days and have the following side effects, flu like symptoms also with sore limbs, sore glands, headaches
I had a very bad chest infection for 6 weeks was on doxycycline 500 for two weeks alongside
prednisone
steroids for 6 weeks I have been put on Montelukast 10mg once a night for 8 weeks been on them 9 days and have the following side effects, flu like symptoms also with sore limbs, sore glands, headaches
Lynne1a
in
Asthma Community Forum
8 months ago
Taper Complete…
I have stopped taking
prednisone
after 18 months of use and slowly reducing the dose. It has been just 2 weeks, so I know my PMR misadventure will still be ongoing. I am very grateful for the support and insight that I have received via this online group. I have been doing okay in terms of pain.
I have stopped taking
prednisone
after 18 months of use and slowly reducing the dose. It has been just 2 weeks, so I know my PMR misadventure will still be ongoing. I am very grateful for the support and insight that I have received via this online group. I have been doing okay in terms of pain.
LabradorH
in
PMRGCAuk
8 months ago
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Christmas Covid
I’m not sure what to do meds wise as I took my 15mg of MTX yesterday as normal and 5mg of
prednisone
this morning that I take daily. Can’t speak to any one and 111 is a waste of time
I’m not sure what to do meds wise as I took my 15mg of MTX yesterday as normal and 5mg of
prednisone
this morning that I take daily. Can’t speak to any one and 111 is a waste of time
Alan7690
in
NRAS
8 months ago
First three weeks on Prednisolone !
It has been a slow start on
prednisone
for PMR, after three weeks there is improvement apart from right shoulder still painful, doctor thinks that could be something else, that could do with some physio . I am still feeling anxious taking the medication.
It has been a slow start on
prednisone
for PMR, after three weeks there is improvement apart from right shoulder still painful, doctor thinks that could be something else, that could do with some physio . I am still feeling anxious taking the medication.
Mistyfied
in
PMRGCAuk
7 months ago
Coming Off Calquence (
We tried
prednisone
for 3 years but every time they took me off my hemoglobin would drop and eventually it was determined I needed treatment. As of now my numbers are looking really good and I'm considering going off of it. I feel like it's keeping me fatigued and impacting my memory.
We tried
prednisone
for 3 years but every time they took me off my hemoglobin would drop and eventually it was determined I needed treatment. As of now my numbers are looking really good and I'm considering going off of it. I feel like it's keeping me fatigued and impacting my memory.
susq9948
in
CLL Support
7 months ago
Helpful forum
My head CT was negative .He says to consider Actemra infusions so I can reduce my
Prednisone
. Yesterday my CRP dropped to 6.5, and sed rate to 6. Your thoughts. I value your knowledge and experiences. Thanks!
My head CT was negative .He says to consider Actemra infusions so I can reduce my
Prednisone
. Yesterday my CRP dropped to 6.5, and sed rate to 6. Your thoughts. I value your knowledge and experiences. Thanks!
Bummed24
in
PMRGCAuk
7 months ago
Optic nerve narrowing
Currently on 15mg
prednisone
. Stopped Actemra 2 months ago. My eyesight in my left eye has been changing rapidly over the past several months. It's gotten really blurry. I've never needed glasses for distance, but now it's hard to drive at night or see the TV very well.
Currently on 15mg
prednisone
. Stopped Actemra 2 months ago. My eyesight in my left eye has been changing rapidly over the past several months. It's gotten really blurry. I've never needed glasses for distance, but now it's hard to drive at night or see the TV very well.
potterylady
in
PMRGCAuk
9 months ago
what should I expect to possibly happen
I plan on bringing extra
prednisone
but I hate the thought that I may have to go back up once again. I can’t belive they can’t make an exception since I am going away. Fingers crossed.
I plan on bringing extra
prednisone
but I hate the thought that I may have to go back up once again. I can’t belive they can’t make an exception since I am going away. Fingers crossed.
Plains
in
PMRGCAuk
8 months ago
Hello ~ New here
I was lucky the Dr I first saw got me quickly to a RA Specialist (I'm still surprised we even had a specialist on our island) anyway, she had me on 20mg
Prednisone
. In Aug she started me on Kevzara 2x mo. We then started tapper in the
Prednisone
1mg every 2 wks.
I was lucky the Dr I first saw got me quickly to a RA Specialist (I'm still surprised we even had a specialist on our island) anyway, she had me on 20mg
Prednisone
. In Aug she started me on Kevzara 2x mo. We then started tapper in the
Prednisone
1mg every 2 wks.
Islandgirlvi
in
PMRGCAuk
8 months ago
Withdrawal vs Secondary Adrenal Insufficiency
I haven't replied because my situation seems to be overcomplicated for many reasons, not the least of which I believe to be the absorption rate of
prednisone
.
I haven't replied because my situation seems to be overcomplicated for many reasons, not the least of which I believe to be the absorption rate of
prednisone
.
nuigini
in
PMRGCAuk
8 months ago
GCA Flare~~ status and explanations💞
I'm taking 60 mg of
Prednisone
per day. I'm happy that it is there for me, but it puts me in low gear ~~pred-head makes me feel like I had all those glasses of wine I denied myself. I'm all about a positive attitude; I'm not depressed, just subdued for me; sometimes, I feel like a spectator.
I'm taking 60 mg of
Prednisone
per day. I'm happy that it is there for me, but it puts me in low gear ~~pred-head makes me feel like I had all those glasses of wine I denied myself. I'm all about a positive attitude; I'm not depressed, just subdued for me; sometimes, I feel like a spectator.
Grammy80
in
PMRGCAuk
12 days ago
Glaucoma and steroids
So I believe I have steroid glaucoma due to his failure in not only checking my medication list that included
prednisone
but failure to monitor my treatment properly. Added to this a fear that my optic nerve has been damaged.
So I believe I have steroid glaucoma due to his failure in not only checking my medication list that included
prednisone
but failure to monitor my treatment properly. Added to this a fear that my optic nerve has been damaged.
Eyak1971
in
Kidney Transplant
7 months ago
copd sucks
Good morning everyone My copd as got so bad over the past 4 weeks and to top that off I have a bad chest infection and the flu , The hospital gave me a nebuliser to take home and I can use it two times aday morning and evening and it’s working so much better than my pumps and I’m also on
prednisone
Good morning everyone My copd as got so bad over the past 4 weeks and to top that off I have a bad chest infection and the flu , The hospital gave me a nebuliser to take home and I can use it two times aday morning and evening and it’s working so much better than my pumps and I’m also on
prednisone
Sweetapple51
in
Lung Conditions Community Forum
7 months ago
New treatment plan GCA
Initially I was told that I would be on Actemra for one year with
Prednisone
and then Methotrexate. Yesterday, I was informed that there will be no Methotrexate and from month ten, I move to fortnightly Actemra injections to extend it out. I am curious to know if anyone has tried this method?
Initially I was told that I would be on Actemra for one year with
Prednisone
and then Methotrexate. Yesterday, I was informed that there will be no Methotrexate and from month ten, I move to fortnightly Actemra injections to extend it out. I am curious to know if anyone has tried this method?
Bessyg
in
PMRGCAuk
9 months ago
Abiraterone edema management
One of the fun things I am getting as an SE while on lupron/abiraterone/
prednisone
is fluid retention. Edema and getting up to pee 3-4 times nightly (losing 3-4 lbs of weight during the night.) What if anything can be done about this?
One of the fun things I am getting as an SE while on lupron/abiraterone/
prednisone
is fluid retention. Edema and getting up to pee 3-4 times nightly (losing 3-4 lbs of weight during the night.) What if anything can be done about this?
Derf4223
in
Advanced Prostate Cancer
9 months ago
Diagnosed under 55
Currently on Lupron twice a year, Zytiga,
prednisone
and Evenity (bone strengthening injection). We are in Israel treated at Hadassah. We have four kids ages 12-18.
Currently on Lupron twice a year, Zytiga,
prednisone
and Evenity (bone strengthening injection). We are in Israel treated at Hadassah. We have four kids ages 12-18.
Vegasborn
in
Advanced Prostate Cancer
6 months ago
91% of lupus patients report using steroids to manage symptoms
Such therapies, like
prednisone
, work to reduce the activity of overactive immune cells. To prevent side effects from steroids, doctors typically prescribe the lowest dose necessary for therapeutic efficacy, then wean patients off of the medications.
Such therapies, like
prednisone
, work to reduce the activity of overactive immune cells. To prevent side effects from steroids, doctors typically prescribe the lowest dose necessary for therapeutic efficacy, then wean patients off of the medications.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
3 months ago
Second Opinion
I had additional labs done for any autoimmune issues and my IgG 4 was elevated and I was then told AIP and put on
prednisone
.
I had additional labs done for any autoimmune issues and my IgG 4 was elevated and I was then told AIP and put on
prednisone
.
TiffanysPancreas
in
Chronic Pancreatitis Support
7 months ago
Rheumatology working up new disorder.
Despite my desire to accept my condition as is and without
prednisone
the Rheumatologist has decided to work me up for a rare autoimmune disorder called Antisynthetase Syndrome. Althernative working diagnose is myositis r/t long term use of statins.
Despite my desire to accept my condition as is and without
prednisone
the Rheumatologist has decided to work me up for a rare autoimmune disorder called Antisynthetase Syndrome. Althernative working diagnose is myositis r/t long term use of statins.
SMH4CRNA
in
PMRGCAuk
2 months ago
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