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Medrol Dosepak
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Overactive bladder
It is my husband who has Parkinson's, but i see many of you Parkies have over active bladder. The medication cost of Detrol LA,capsules, or it's generic, tolterodine tartrate, is very expensive, I figured it is about $5 a pill. I can't get along without it unless i want to be up 7 times a night to the
It is my husband who has Parkinson's, but i see many of you Parkies have over active bladder. The medication cost of Detrol LA,capsules, or it's generic, tolterodine tartrate, is very expensive, I figured it is about $5 a pill. I can't get along without it unless i want to be up 7 times a night to the
rhyspeace12
in
Cure Parkinson's
7 years ago
Nutri Adrenals - feedback wanted
I realise there have been many posts written on this subject, but thought it preferable to start a new one: I have been wondering if I should try Nutri Adrenals as it seems (this is how interpret previous posts here) that they actually help heal the adrenals? I was diagnosed with adrenal fatigue back
I realise there have been many posts written on this subject, but thought it preferable to start a new one: I have been wondering if I should try Nutri Adrenals as it seems (this is how interpret previous posts here) that they actually help heal the adrenals? I was diagnosed with adrenal fatigue back
Hidden
in
Thyroid UK
7 years ago
Depo-Medrone 12l Intramuscular
Hi everyone. I have been having the above steroid jabs in my bum. The Rheumatology Nurse does one at the hospital (& between her & my Consultant I have the usual checks). Three months later the next jab is done at my GP Surgery. My last jab was booked at my surgery for 12 July. Fine. Then I received
Hi everyone. I have been having the above steroid jabs in my bum. The Rheumatology Nurse does one at the hospital (& between her & my Consultant I have the usual checks). Three months later the next jab is done at my GP Surgery. My last jab was booked at my surgery for 12 July. Fine. Then I received
Blackwitch
in
NRAS
7 years ago
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Solumedrol
Hello all!!!!! Today I start 3 freaking days of steroids!!!! I hate steroids! They totally mess with my diabetes! The next 6 days of my blood sugars are going to suck!!!! No carbs for me. Grrrrrrrr. So if you all could say a prayer I get ahead of the high sugars and exhaustion to follow. I would be most
Hello all!!!!! Today I start 3 freaking days of steroids!!!! I hate steroids! They totally mess with my diabetes! The next 6 days of my blood sugars are going to suck!!!! No carbs for me. Grrrrrrrr. So if you all could say a prayer I get ahead of the high sugars and exhaustion to follow. I would be most
rlh1974
in
My MSAA Community
7 years ago
Medrol
Hi :) In two weeks, I'm going to start taking Medrol (methylprednisolon), corticosteroid, due to my liver problems. My hepatologist told me that I will be on 32 mg at start but then during 2 months I will be geting down to 4 mg, and then I'm supposed to be on 4 mg for 6 months. Does someone have experience
Hi :) In two weeks, I'm going to start taking Medrol (methylprednisolon), corticosteroid, due to my liver problems. My hepatologist told me that I will be on 32 mg at start but then during 2 months I will be geting down to 4 mg, and then I'm supposed to be on 4 mg for 6 months. Does someone have experience
Ana1806
in
British Liver Trust
7 years ago
2nd half-dose Ocrevus Infusion Completed
As many of you following Ocrevus news and experiences are aware, the first 600 mg. dose of Ocrevus (ocrelizumab) is divided into two half-doses spaced two weeks apart. I posted earlier about my first infusion ("Ocrevus - Tomorrow's the Day"), and yesterday I completed the second infusion installment.
As many of you following Ocrevus news and experiences are aware, the first 600 mg. dose of Ocrevus (ocrelizumab) is divided into two half-doses spaced two weeks apart. I posted earlier about my first infusion ("Ocrevus - Tomorrow's the Day"), and yesterday I completed the second infusion installment.
dianekjs
in
My MSAA Community
7 years ago
Face rash - anything besides the sun??
Hi all! Tossing this out there b/c I've become really frustrated with both my rheumy and my dermatologist. They are both really great but beyond saying "yeah, that's the rash" they are soooo not helpful. No matter how much sunscreen I put on (I do all over body and at least three layers on my face +
Hi all! Tossing this out there b/c I've become really frustrated with both my rheumy and my dermatologist. They are both really great but beyond saying "yeah, that's the rash" they are soooo not helpful. No matter how much sunscreen I put on (I do all over body and at least three layers on my face +
katidid
in
LUPUS UK
7 years ago
Groin pain flare = inflammatory arthritis?
I'm currently diagnosed with UCTD plus possible fibromyalgia. In the last six weeks I've had two episodes of a new 'crisis' - groin pain that I'm guessing is coming from the hip joint. Does this sound familiar to anyone? I have had mild pain in both hips (really the grease of my groin, on both sides
I'm currently diagnosed with UCTD plus possible fibromyalgia. In the last six weeks I've had two episodes of a new 'crisis' - groin pain that I'm guessing is coming from the hip joint. Does this sound familiar to anyone? I have had mild pain in both hips (really the grease of my groin, on both sides
LuckyJC
in
LUPUS UK
7 years ago
New to Humira - curious if others had similar experience?
Good morning, fellow warriors. I wish mine WAS a good morning, but not so much. I should start out by saying I DO plan to talk to my rheumy on Monday, but since it's the weekend and I have to wait for his input, I thought I'd seek some comfort here - if nothing else, knowing I'm not alone helps! Took
Good morning, fellow warriors. I wish mine WAS a good morning, but not so much. I should start out by saying I DO plan to talk to my rheumy on Monday, but since it's the weekend and I have to wait for his input, I thought I'd seek some comfort here - if nothing else, knowing I'm not alone helps! Took
gatodelsol
in
Cure Arthritis Community
7 years ago
Finally I become of Imbruvica's family
My fifth day Imbruvica. What to expect and what to keep as a young patient ? Blood picture from today- chronic progressive ;) Still on corticosteroids 2*4 mg Medrol! I feel boringly normal...хахахахх Best regards CLL friends! Cervus_dama
My fifth day Imbruvica. What to expect and what to keep as a young patient ? Blood picture from today- chronic progressive ;) Still on corticosteroids 2*4 mg Medrol! I feel boringly normal...хахахахх Best regards CLL friends! Cervus_dama
Cervus_dama
in
CLL Support
7 years ago
RECURRING PMR SYMPTOMS OR ANOTHER CONDITION?
I began weekly depo-medrol injections for PMR on August 25, 2016, and have been tapering since November 15. Two weeks ago my daily dose dropped to an estimated 2.0 mg and I experienced 4 consecutive days with stiffness in my hands and mild-moderate shoulder pain. When I went back up to 2.5 mg, the symptoms
I began weekly depo-medrol injections for PMR on August 25, 2016, and have been tapering since November 15. Two weeks ago my daily dose dropped to an estimated 2.0 mg and I experienced 4 consecutive days with stiffness in my hands and mild-moderate shoulder pain. When I went back up to 2.5 mg, the symptoms
Admiral06
in
PMRGCAuk
7 years ago
Just ended day 3 of Solumedrol
I hated to do it, but I've spent the last 3 days getting IV steroids from Home Health Care. The exacerbation hadn't gotten too bad yet, but it was spreading and the neuro wanted to nit it in the bud. The worst part of the steroids for me is the sleep disturbance. I've been up and down at night, sleeping
I hated to do it, but I've spent the last 3 days getting IV steroids from Home Health Care. The exacerbation hadn't gotten too bad yet, but it was spreading and the neuro wanted to nit it in the bud. The worst part of the steroids for me is the sleep disturbance. I've been up and down at night, sleeping
Iona60
in
My MSAA Community
7 years ago
Does Flu and Colds makes the platelet count drops to low level?
My child was confined 2 weeks ago and he received IvIg for 1 day and Solumedrol 870mg for 3 days and no medication at home.....after a week his platelet went up to 359k and after a week again his platelet went low to 29.6k without any petechiae, hematoma and bleeding. ( my son is a bleeder his bleeding
My child was confined 2 weeks ago and he received IvIg for 1 day and Solumedrol 870mg for 3 days and no medication at home.....after a week his platelet went up to 359k and after a week again his platelet went low to 29.6k without any petechiae, hematoma and bleeding. ( my son is a bleeder his bleeding
DavieSimon
in
ITP Support Association
7 years ago
Loss of sight scare
Hi Everyone, Hope all are well, coping, with these inflammatory conditions. I am just home from a NYC Hospital w an event that was truly frightening. And again it concerned doctors, claiming to be "experts" in GCA, and not knowing what the h--- they were doing. After 2 bouts of penicillin, I walked
Hi Everyone, Hope all are well, coping, with these inflammatory conditions. I am just home from a NYC Hospital w an event that was truly frightening. And again it concerned doctors, claiming to be "experts" in GCA, and not knowing what the h--- they were doing. After 2 bouts of penicillin, I walked
Whittlesey
in
PMRGCAuk
7 years ago
CT3M
I know members here have used the CT3M method successfully, and I'd love to hear about your experiences. I managed to wean myself off Medrol (prescribed for adrenal fatigue in late 2011) about a year ago. HC never worked for me as it metabolised too quickly. I was diagnosed with adrenal fatigue based
I know members here have used the CT3M method successfully, and I'd love to hear about your experiences. I managed to wean myself off Medrol (prescribed for adrenal fatigue in late 2011) about a year ago. HC never worked for me as it metabolised too quickly. I was diagnosed with adrenal fatigue based
Hidden
in
Thyroid UK
7 years ago
should cortisone always be combined with DHEA?
The Hertoghe doctors say you need to take DHEA with hydrocortisone or Medrol (unless you also suffer from PCOS). The reason is that DHEA will prevent cortisone from "eating up" too much tissue. Therefore, you are handed a prescription for DHEA along with your prescription for cortisone. Last year, my
The Hertoghe doctors say you need to take DHEA with hydrocortisone or Medrol (unless you also suffer from PCOS). The reason is that DHEA will prevent cortisone from "eating up" too much tissue. Therefore, you are handed a prescription for DHEA along with your prescription for cortisone. Last year, my
Hidden
in
Thyroid UK
7 years ago
Steroid induced Shingles?
Hi everyone, I'm new here and am wondering if anyone else has experienced Shingles as a result of Steroids? I was diagnosed about 18 months ago with seropositive RA. I take MTX and Hydroxychloroquine. I had an initial Depo-Medrone jab to help until the drugs kicked in. All was well until I had a bad
Hi everyone, I'm new here and am wondering if anyone else has experienced Shingles as a result of Steroids? I was diagnosed about 18 months ago with seropositive RA. I take MTX and Hydroxychloroquine. I had an initial Depo-Medrone jab to help until the drugs kicked in. All was well until I had a bad
SoulmanPaul
in
NRAS
7 years ago
synthetic corticosteroid
Solumedrol IV treatment- people are willing to use a synthetic corticosteroid when turmeric or frankincense oil or extreme high doses of Vitamin D3 can help, curious as to the why's?
Solumedrol IV treatment- people are willing to use a synthetic corticosteroid when turmeric or frankincense oil or extreme high doses of Vitamin D3 can help, curious as to the why's?
Fuzzman
in
My MSAA Community
7 years ago
Acupoints Massage Therapy For PPMS
For years I tried to reach out for PPMS patients like me. Since 1995, I was diagnosed with Fibromyalgia and IBS. In year 2000, I was confirmed with Spinal Cord MS. Injections and oral medications (except Elavil) did not slow down my progression. In 2011, I was in the hospital and came home in wheelchair
For years I tried to reach out for PPMS patients like me. Since 1995, I was diagnosed with Fibromyalgia and IBS. In year 2000, I was confirmed with Spinal Cord MS. Injections and oral medications (except Elavil) did not slow down my progression. In 2011, I was in the hospital and came home in wheelchair
yuehmei56
in
My MSAA Community
7 years ago
Solumedrol
I'm on to second of five Solumedrol iv treatment. I'm a paraplegic fighting to save my upper body. Right side ok but left is numb, tingling and plain dumb sometimes.
I'm on to second of five Solumedrol iv treatment. I'm a paraplegic fighting to save my upper body. Right side ok but left is numb, tingling and plain dumb sometimes.
karenmbloom
in
My MSAA Community
7 years ago
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