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Long term side effects of Evenity

Osteoporosis & Bone Health | Last Active: 30 minutes ago | Replies (41)

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@dianestanley

I took the 12 shots of Evenity ending in July 2023. I am supposed to take Prolia twice per year. I don't know how that will go yet. It is my understanding that after you take Evenity, you need to take something else so that you don't lose the good that the Evenity has done. I get the first Prolia shot next week. After Evenity, my spine surgeon feels that my bones are better and he can now do surgery to fix my issues in my back.

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Replies to "I took the 12 shots of Evenity ending in July 2023. I am supposed to take..."

Thanks for sharing this

Hi! I’m Kathryn and I’m going on 82 years old. About 23 years ago I was diagnosed with Panhypopituitarism which means I don’t have a pituitary gland anymore. It took me nearly ten years and seeing many doctors to get a firm diagnosis. By that time I had all sorts of physical problems, one of the worst is osteoporosis. My entire back is a real mess with rampant spinal stenosis and many broken discs. Several years ago I was talked into getting back surgery which was a huge error as the surgeon made a giant mistake. The head of the hospital got in touch with me and told me of the surgeon’s error and advised me to get an attorney. I did just that and won the case. It really doesn’t matter if one receives financial recompense if one has ended up with worse pain than was present before the surgery.

I have a very difficult time getting the amount of exercise that I feel would be beneficial given my physical condition. The residual effects one gets as a Panhypopituitary patient are many - one is losing a great deal of bone tissue which has caused me to lose three inches in height which won’t grow back. The level of pain I now live with stops me from living some sort of normal life. I take lots of replacement hormones and many other types of meds as the Panhypopituitarism is really tough on the body as a whole.

If there’s anyone reading this message who has also experienced Panhypopituitarism and is trying to develop some semblance of a normal life, please share your experiences. Thanks ever so much!