Hesitant to begin drug treatment for my osteoporosis
Hello! My first post here as a new member. I am an active 69 year old female who was diagnosed many years ago with osteopenia but now have osteoporosis. When diagnosed with osteopenia I gave several drugs a try. I had side effects from all the oral choices I took, and when giving myself Forteo shots, broke out in hives all over my body. After that, I decided I would take my chances and go the natural route to keep my bones healthy with diet, consistent exercise and Calcium/Vitamin supplements. Fast forward to present time my last bone density scan was worrisome, (a -4,4 T score in my spine). An endocrinologist strongly suggested treatment, (shots or infusions), but I still fear side effects. I am currently trying to educate and empower myself by researching all options. I am already a bit overwhelmed with so many differing opinions. Drugs or no drugs?! The possible serious side effects of drug treatment still frighten me. Has anyone here diagnosed with more advanced osteoporosis, remained fracture free? Am I at such a high risk that I’m doomed without drug treatment? Thank you in advance for any advice, experiences, etc.
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I concur with your thoughts @windyshores. -4.4 is a serious number and even though I am personally reticent to take potent drugs, I wouldn’t hesitate with a score like that. As you know, I started a bio-similar to Forteo because of my-3.1 spine score and suffered uncommon, serious side effects for the first 5 weeks (heart palpitations, chest pains, severe fatigue). I stuck it out hoping my body would adapt and it did!! I’m over two weeks without any symptoms thankfully.
I’m hopeful I get the same results you did, and I’m already considering trying Evenity afterwards. I’ll talk to my endocrinologist in 22 months about that:). I may just do Reclast, then take a 3 year break, then start Evenity. Not sure yet, but my fear of taking the drugs has been trumped by my worry of not being able to be active into my 70s and 80s!!
Thanks again for your time and contributions to the people on this site. It’s been invaluable to me.
@lynn59 what heroic persistence and I am so glad your body adjusted. Yay! Look forward to hearing your results!
@lolamarie why did you lose hope about Tymlos? I had amazing gains. Many others have posted on their success in getting onto a therapeutic dose by starting with 1/4 dose and moving up. That option should be reassuring for you. I had NO side effects on 1/4 dose and after maybe 6 weeks I could do 7/8 dose very tolerably, even though initially a half dose was torture. I hope you will try this. I actually miss my Tymlos!
Oh my that does seem like a bad dexa scan number. May I ask what your height and weight is? I am 4 11 and weigh 125. I also question my numbers because of being petite but doctors don't agree.
Has anyone went on Fosamax after finished the Tymlos injections?
Good evening, @grammy9. After two years of Tymlos, I was told to begin Prolia. That was a huge mistake for me. So, my new Mayo endocrinologist changed the option to Fosamax (alendronate). I will complete two years next month, so I have scheduled a Dexascan. I am anxious to see how well my bones are performing.
May you have happiness and the causes of happiness.
Chris
Thank you for replying. I have heard so many bad things about Prolia and worried they will try to give me that after I finish treatment. Thank you so much for your information.
@grammy9 you can be in control of what you take for medications!
I know but it's hard to decide which is best. I was on fosamax for 9 years. My dexa scan kept getting worse and my doctor sent me to specialist. They suggest tymlos...forteo or evenity. With bone cancer and heart issues with them it's terrifying.
Forteo and Tymlos do not cause bone cancer. Not a single human case. That is old information.
We posted above about Evenity and heart issues. I have afib and had no hesitation taking it.