Google
The Young and the RA » Blog Archive » PREDNISONE: Jagged little pill The Young and the RA

PREDNISONE: Jagged little pill

prednisone

Prednisone. That little miracle drug. Most people with RA have been put on prednisone at some point during their life. When I was experiencing the symptoms of RA (before they knew what I actually had), I was put on prednisone. I remember hobbling out of the pharmacy and popping that first little white pill into my mouth, and it was like magic! I practically skipped the entire way home! I hadn’t been able to move like that for months! And that was only within a few minutes of taking the drug! Wow! I should just stay on this forever! I learned, while on prednisone, that if I took the drug around 7 a.m., even before I was officially out of bed, I would wake up without any morning stiffness. How fabulous!

Prednisone is a drug that is used:

“to treat the symptoms of low corticosteroid levels (lack of certain substances that are usually produced by the body and are needed for normal body functioning) […] Prednisone is in a class of medications called corticosteroids. It works to treat patients with low levels of corticosteroids by replacing steroids that are normally produced naturally by the body. It works to treat other conditions by reducing swelling and redness and by changing the way the immune system works” (MedlinePlus).

Because of the way the drug works, I was told it was best to take in the morning, but consult your doctor about when you should take it. When you take it can be almost as important as the dose in relieving the pain caused by RA. 

When I first started taking prednisone, I felt amazing! It was as if that tiny little white pill solved all my problems! Unfortunately, I soon experienced the nasty side effects of this so-called miracle drug. I started breaking out in acne like I was back in middle school. My face became extremely round (they call it moon face). I had irregular periods, tiredness and gained weight. According to MedlinePlus, prednisone has the following side effects if take for any extended period of time:

  • “headache
  • dizziness
  • difficulty falling asleep or staying asleep
  • inappropriate happiness
  • extreme changes in mood
  • changes in personality
  • bulging eyes
  • acne
  • thin, fragile skin
  • red or purple blotches or lines under the skin
  • slowed healing of cuts and bruises
  • increased hair growth
  • changes in the way fat is spread around the body
  • extreme tiredness
  • weak muscles
  • irregular or absent menstrual periods
  • decreased sexual desire
  • heartburn
  • increased sweating”

Turns out, prednisone is not the miracle I was looking for. I cannot even begin to describe to you how ugly and horrible I felt when these side effect kicked in. See if you can see the difference. The acne isn’t as obvious in the pictures; I really just look red, but trust me, it’s there.

prednisone-copy.jpg 

It was a terrible experience. I look back at pictures from that time, and I wonder how my boyfriend could ever have been attracted to me (I met a wonderful guy right about the same time I started taking prednisone. He was such a support while my doctors figured out what drugs to get me on. I feel so lucky to have some so amazing and understanding in my life.) Once I got officially diagnosed with RA, I was started on a number of drugs before being put on what I am on today (HumiraImuranmethotrexate). It did however take me quite a long time to get off prednisone completely. For a while, every time the doctors tried to take me off, I would have a flare-up. I was on prednisone for close to nine months before I could get off it, and I had been on methotrexate for over eight of those months and Enbrel for about half of them. Yeah. Longest prednisone taper ever.

 

Now, I do still have a bottle of prednisone tucked away in my bedside table for those horrible days when I wake up with terrible joint pain (my rheumotoligist prescribed it for when I have bad days, but I have to say I only will take a 5 mg pill about once or twice a month now, and that makes me feel great!). I definitely recommend getting a prescription for the occasional flair up if you don’t already have one!

In fact, a new study just came out that found modified-release prednisone is even better than the standard, immediate-release version at reducing morning stiffness in people with RA. The study was done by German researchers at Charite University Medicine Berlin:

“After 12 weeks of treatment, patients taking the modified-release version experienced an average of 44 minutes less morning stiffness per day than at the start of the study. That was 29.2 minutes less than those who took the standard version, the team noted” (washingtonpost.com).

Just remember, prednisone is NOT A VIABLE LONG TERM TREATMENT OPTION!!!! The side effects are so not worth it!

Until next time,

S.P.

*Some of the side effects of prednisone can be serious, if you are currently on the drug and experience any of the above side effects, consult your doctor immediately!!!!!!!!!

7 comments so far

Wow, this story is so so close to my heart. I am 25, and got diagnosed with RA when I turned 21 (on my birthday actually). I had the same experience with it at first. In fact, for the first 2 months, I actually LOST weight. Then, things turned really bad. I have had to be off and on it, in pretty large doses, in between treatments and for what is now a constant flare up. It has basically ruined my body in so many ways that I’d almost rather suffer than be on this stuff. The pictures you have on here so resemble my situation. I was tiny, happy, and balanced. After prednisone, I was swollen/puffy, confused and very up and down in my moods. I also have a wonderfully supportive man in my life, and I sometimes wonder how on earth the physical element is there. I was attractive and vibrant when we met, but shortly after, was what I call “prednisoned-out” and he’s stuck by me. So, thank you for this post. I think it’s really helpful to hear other people, especially young women, who struggle with the same thing. On a positive note- my new treatment seems to be helping a lot more now and I’m only on 5mgs a day. I can’t wait to get to 0 a day, and just use it occassionally like you said. Every time i go below 5mgs though, I flare up again, so it’s going to have to be a slow and steady process. Thanks again for sharing your story!

Jolynn
January 19th, 2008 at 3:41 pm

I totally understand what you went through! Have your doctors started you on any other medications?

S.P.
January 27th, 2008 at 11:11 pm

wow.
you have really helped me so much.
i am 24 and got diagnosed just before christmas.
it is all really really new and scary to me. so, thankyou!

kristy
February 6th, 2008 at 6:19 am

Glad to be of help! I know I was really lost when I first was diagnosed. It is a bit surreal. Let me know if there are any other topics you would like me to cover. Thanks for reading.

S.P.
February 6th, 2008 at 12:11 pm

Hello all…My name is Bob and I’ve had RA for about 5 years now…it started with my left hip having to be replaced and it promptly decided to invade the rest of my joints…my ankles being the most severly affected now. I suffer from incredible pain…and my thyroid gland is underactive. What sucks is that I’m only 50 years old and I had been athletically active for my whole live. My latest malady is constant sleepiness from the prednisone I take. I think we can all agree as RA people we NEVER get what is called ” A good nights sleep” I would fling this prednisone down the street in a heartbeat but it is the only thing that seems to stop making my calves, ankles, and feet look like Coke bottles. I’m on disability and I’m pretty home-bound…I do an internet live sports-talk show from a studio in my home since August of 2005 to keep my sanity. I often wonder if I should get an internet radio show going for all of us that have this unforgiving thing called RA. I have been experiencing the most ridiculous bouts of sleepiness lately…I’m fresh and wide awake from about 6am till 9 or 10am and the rest of the day I’m constantly nodding off. I have no energy to do anything. I wonder if it it just as well to count off the preds and live with the swelling. I am back on Remicade…it’s very expensive…I’m on Medicaid and I had to take extra coverage to bridge the 20% gap to pay for it. I would gladly donate my time to set up a site where we can collectively get together to discuss our RA and to host a radio show to perhaps help us help each other…I so HATE this disease!!!! Bob Merc- spasportsshift@hotmail.com

Bob Merc-The Shift
March 12th, 2008 at 5:34 pm

Oh man.
I am TRYING TO GET OFF Prednisone and it’s been a nightmare!
I am currently looking up info on the internet and found your post.
I have Palpable Purpera and every time I decrease my right ankle swells so much I can barely walk…it’s been almost 3 months and my body wants 20mg a day. (I’ve been trying 15-17 mg)
I didn’t know about taking the meds in the a.m. being better for our bodies… wish someone had told me this in the beginning! I have been taking it throughout the day especially in the EVENING when I seem to swell!

Mikiye Creations
April 26th, 2008 at 6:02 pm

I am 70 pretty good shape.I had a vending buisness(soda snapple candy etc.)very active. Retired april 2006, july 13 2006 I had heart surgery, bad mitral vavle.Survived the operation ok but three months later started to experience pain in joints.Now they say I have RAbeen taking prednisone for 1-1/2 years,last month iwas on 60mg a day for 4 days then 40, 20 etc. Now Iam on 5mg
aug 30 2008 i have so much joint pain its almost unbearable
I also been on Plaquinol,mexo,arava, noting helps. Don’t know what to do.

Bernie
August 31st, 2008 at 7:24 am

Leave a Comment

Name

Mail (will not be published)

Website

Comment