Broken bones due to Prednisone?

I don't think you have been on pred long enough to have bone density issues - but I would speak to your doctor about it - you may be more inclined toward osteoporosis.  I have charkot breaks/fractures in both my feet which has caused them to collapse...but that is after 7 years on and off steroids.

I would definetely get the scan though.

love to all

bob

I agree. I don't think you've been on pred long enough or at a high enough dose to affect bone density, UNLESS you've been on it before for an extended time and/or high dose. However, if you're a small-boned, white female at perimenopausal age, you're already at risk for osteoporosis, pred or no pred.

If you have a doctor's note and are willing to work from home, I don't see how your boss could object.

Thanks for the input.  I've only been on Prednisone for about five weeks now but I was on it for eight months when I was first diagnosed.  Most of that time I was on 20 mg and tapered as tolerated over the eight months.  I'm not sure if that would be long enough to cause bone density issues.   This is so difficult living by myself and having no one to help.  I always put myself out for my family members (most of the time to my detriment) and now when I need help, all I get are phone calls and no one can be bothered to assist for even an hour.    Very depressing and disappointing.  Sorry.  I just needed to vent.  I've never been at such a low point in my life.

I was on pred for about eight months (40mg) tapering on and off during the whole time.   I was sent for a bone density test and found out to my dismay that I'd gone from strong healthy bones to skinny fragile ones, all thanks to the wonderdrug prednisone.

Now I'm on daily calcium and 'D' plus a fortnightly dose of fosavance (70mg) just to ensure they don't get any worse.

My knees and hips are starting to give me some gyp too but I suspect that is a joint/cartilage problem (probably arthritis) and might have nothing to do with prednisone, although it makes you wonder.

I can only hope I never have to take it again.

Considering your age you should be able to get your bones back to normal with calcium.

 

I think the most disturbing part of this post is that fact that nobody will help you when you need it most.  Sorry to hear you're not getting the physical/emotional help you need.  Guess that's where we come in.  At least on this board, we can talk to each other, and everybody here will understand what you're going through.  That way, you know you're not alone.  Whenever you need support, we're always here for you (and everyone else).

Eight months is a long time to be on pred, although 20 mg is a relatatively low dose. Bone thinning could have taken place during that time, although you won't know for sure what's going on until you have a scan. That's definitely a good idea... and it's quick, non-invasive and painless.

If you do find you have osteopenia - the precusor to osteoporosis - calcium supplementation will help, but more importantly... weight bearing exercise and weight training made a huge difference for me.

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Diagnosed with ulcerative colitis spring 1999

Ive been on pred for about 8 weeks, and im schedualed for a bone density test next Tuesday, just so we have a base line to start on. That way, if I have to continue with the pred. they have something to go by and can tell if there is any bone loss or not. It would be a wise thing to get done, just to have the information ready. Its only a 10 minute test.

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Just diagnosed Aug. 14/07

I'm so sorry that you feel so alone. I've felt that way and it's a horrible feeling. In my case, it was my brain imagining I was alone. Not saying that's what's happening to you because I don't know, but I will concede that it is an awful feeling.

Please know that others here would be there for you physically were you close by, but in the meantime, we would like to be there for you via cyberspace. We all know what you are going through with this illness, and some of us understand the aloneness that you are feeling as well.

It always helps me to imagine that others are thinking about me, as I think about them, and recognize that we are never so alone as we think we are. Some people just do not understand that you really, really need help unless you hit them over the head with it. Perhaps it's time to be more assertive and/or explain to them that their lack of response makes you feel alone, and that on top of your illness really hurts you. Ask them if you can count on them for X, Y or Z (be very particular) and see if they don't respond.

If they don't, I'm sure that will hurt. But remember that we are here for you, albeit not in the face-to-face way.

Mitz

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Sporadic proctitis since about 1985. Mother had UC, then J-pouch surgery 1983.
DX'd with clostridium difficile in 2000. Prednisone, two courses of Flagyl, then Vancomycin finally got rid of it. Symptomatic with UC after that.
Colonoscopy in 2001 dx'd left-sided UC. Was pretty darn ill at that time. Treated with prednisone, Rowasa, Asacol. Asacol not working so switched to Imuran. Three small flares since in 2002, 2005, and 2007.
Gall bladder attack 6/13; ultrasound showed stones; surgery before end of 2007.
100 mg Azathioprine and 225 mg Effexor XR (for chronic, longstanding depression) daily.

masscs - sorry to hear that your family is not there for you! This is a difficult disease to deal with. I'm so glad to have the support of this forum :) There is usually someone on at any time. I've gotten the lift I needed and the kick in the pants when needed too from my friends here.

Venting is always allowed here! Plus you know we'll understand and not tell you - it's all in your head or maybe you should eat better! Grrr... Those lines make me crazy!

Hang in there :)

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Pan-colitis and GERD diagnosed May 2003

 

Asacol 12 per day,  Azathioprine 75mg, Rowasa and Canasa as needed

Aciphex, Effexor XR, BCP, Rhinocort nasal spray

Forvia and a Probiotic

 

Osteopenia (hip and spine) from prednisone use.  Started Azathioprine because I was steroid dependent.

 

Co-Mod for the UC forum

Keep HealingWell running smoothly:  www.healingwell.com/donate

Thanks for the support and suggestions everyone.  Once I'm able to get around again, I will make sure I go for a bone denisty test.  Also, my sister has come through and has really helped me out the last few days so I am getting a lof of family support now.  I've also learned to speak up and ask for help for things that I specifically need.   Unfortunately, I was having a lot of pain in the calf of the foot that I broke and my sister took me to the hospital yesterday.  Turns out, I now have a blood clot in my right leg behind my knee! It's been going from bad to worse!  To top it off, I had tapered the Prednisone a few days ago to 35 mg and seemed to be doing well but after I came home from the hospital last night, had a lot of blood and spent the night going back and forth to the bathroom.  I just can't seem to catch a break. 

Thanks again everyone.  I'm sorry that there are so many of you who are experiencing this lousy disease but it's good to know I'm not alone anymore!  And I have to agree with some of your comments about being sick of people who tell us to "stop stressing" and make sure you "eat right".  The nurse at the orthopedic doctor's office told me she "used to have colitis".  I asked her what she meant by "used to".  She said she had it 25 years ago and once she stopped "stressing out", that she was fine. 

I was on Pred for almost a year, then switched to Entocort because it was supposed to have fewer of the bad side effects. I was taking Calcium and vitamin D from the start, because I knew about the osteoporosis issue. In total, I was on steroids for about five years because I got desparately sick every time I tapered off of them.

I broke both of the bones in my lower left leg, and still don't know when it happened. Because I have a lot of trouble with the joint pains sometimes associated with UC, I didn't go to the doctor right away, so ended up having to have surgery.

Now I've had two shoulder surgeries because the steroids caused an extremely painful avascular necrosis which was killing the boney tissue.

I don't know if I could do anything differently if I had it to do over again, because at that time none of the newer treatments were approved for UC. Now, I'd much rather take Remicade and take my chances on its side effects than to let steroids painfully destroy my bones.

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