My Experience on Evenity for Treating Osteoporosis
Thought I would share for those considering or on Evenity for osteoporosis:
Afer much research and discussions with my GP and Cardiologist, I have decided to start my treatment with Evenity injections. As with all drugs, there are many side effects. My biggest concerns were stroke and heart attack. However, considering that I do no have any history for either, for me personally, the benefits outweigh the risks. As my GP said to me, "if everyone only thought about the side effects of the drugs, no one would be taking them".
I had my first injections (subcutaneously in the back of each arm) on June 30th. The nurse that administered the injections discussed the drug in depth, along with all the possibilities that may occur. She also mentioned that for all the patients that she has seen, none has had any side effects.
The injections are once a month for only one year, so I'm hoping that this works well for me and I can improve my bone density, especially in my spine, where I need it the most.
My endocronologist has also prescribed Hydrochlorthiazide for my idiopathic hypocalcemia. I have an appointment with an allergist this month to confirm whether I still have an allergy to sulfa drugs, since this drug contains sulfa. Apart from this I take D3 orally and try to obtain additional calcium through foods not supplements. Trying to walk 3-4 times a week and will begin with a few weight bearing exercises.
My journey began September, 2019 when I was diagnosed with severe osteoporosis. After waiting to see three doctors, receiving three denials from insurance company for Evenity, which took several months, I am hopefully on my way for a favorful outcome.
Interested in more discussions like this? Go to the Osteoporosis & Bone Health Support Group.
What did you do for pain from spine fractures? I have 3, 2 were treated with kyphoplasty, the first fracture(T12) couldn’t be treated , assuming 8 months pain is from that one. I take some pain meds but nothing relieves it.
I chose not to do kypholasty. My doc said outcome wasn't that different. I avoid lifting, spend time in bed, take a walk every day and do tai chi. I try to accept the pain. The hard part for me is not being able to open windows or lift things. I get neuro effects like nerve pain and numbness and if I make a mistake my entire spine hurts, as well as toes, legs, arms and neck. Sympathies!
I don't take pain meds usually though if I do something that causes a problem I take tylenol or ibuprofen.
I had kyphoplasty at T-12 last year. No more pain from that location, just the degenerative arthritis pain in low back.
I am very interested in the patient assistance for Tymlos . I would appreciate the details.
I tried to get assistance on the Prolia shot and the Evenity shot but most places I called said there was no funds available .
Amgen, the company that makes Evenity and Prolia, does not have a patient assistance program (though sometimes funds are available through a foundation).
Radius makes Tymlos and has the Radius Assist program. The application is on the Radius website but you need to first contact Tymlos Together. They will assign you a personal representative who can help you with the Radius Assist program.
Thanks for the information. I will definitely look into this .
I thought, but can't swear to it, that I read that there's a school of thought that smaller doses of bisphosphonates in general work well. If I recall correctly it was a study suggesting that bisphosphonate dosage recommendations are too high. So maybe a lower dose will be fine.
My doc is cautious due to my sensitivities. He may plan to increase the dose if I feel fine on a low dose, which I doubt will happen. If you have that study, others would benefit if you post it.
I have a spinal cord injury. I am 3 weeks into my treatment. I had a Reclast shot on December 31, 2021. It is still active for at least a year. Because my Osteoporosis is so bad, my Endocrinologist and Rheumatologist wanted me on both meds. I am having extreme weakness. The weakness and muscle twitches started the first day I had the injections. I want to stay on Evenity to strengthen my bones. I do not want to struggle harder than I already do to walk and get around. On the flip side, I want to have a surgery I need and I do not want to keep fracturing my bones when I fall or twist.
Hi, I started Evenity shots in July of this year. I can appreciate your comment about keeping your calcium levels up. I had a wellness visit with my primary care doctor this week and the blood labs showed low calcium and parathyroid hormone flagged as High. It was more than double my previous year's level. I make an effort to eat as many high-calcium foods as I can, plus supplement. So, I'm not sure why I had those bad levels. I see my endocrinologist tomorrow and we will discuss and hopefully take whatever steps to resolve.