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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How long from the time you send in your records to when you have your consultation? I hope it’s not MONTHS but if I have to wait that long, it’s not any worse than scheduling an appointment with my endocrinologist.
It could be a couple of months, but you can just call them and find out before you book anything. You don't pay in advance, by the way, so that makes it more flexible.
I haven't spoken to him in a year because I'm pretty much on auto-pilot taking Tymlos. I may call him when it comes time to decide what is next.
Sounds like you are doing well with these meds. I was under the impression it was not good to take these after 5+ yrs due to easily fracturing a bone. So when I was told I would only have to take it for two years I was ok with that. Sounds like it your numbers improve significantly they want you to continue to take the meds. I guess I will cross that bridge when I get it it! I was wondering after seeing there are other medication options to choose from why my doctor decided on Fosamax.......could be insurance coverage I suppose. I took my 5th pill this morning and I am still not experiencing any side effects.
I hate the words "compression fracture". Sounds very painful. Thanks so much for sharing your story.
Looking back, I would not take Fosamax for more than three years. It's occurred to me that being on Fosamax for so long might have contributed to my fracture but when I asked my endocrinologist if that might be the case she denied it as a cause. She thought that the Fosamax just stopped working and was not stopping my bone loss.
I won't have another DEXA until next year but I am hoping the anabolic medication plus the resistance training, supplements, and nutrition will have helped.
Thank you for your advice. That is good information and does correlate with other things I have read that the medication does stop helping the bone loss. Do you still get your DEXA every two years while taking the meds? I was wondering if you have to wait two years before knowing if the medication is helping.
Typically, the doctor will want a DEXA every year. Along the way, he will likely order blood tests for P1NP and CTX: the two bone markers that indicate if the medication is working.
Thank you!
Hello Lilac,
Thank you for sharing. Pleased to meet you!
I’m new too, and pleased to have found someone in a similar place age, spinal density and preferring the natural route until the next test, then re-evaluate.
I did the REMs test which was encouraging! It indicated my bone quality was fairly good, better than the density. I was not surprised as I am clumsy and fall often yet never break bones. I’ve been told I’m very graceful when falling 😂 Mind you after my Dx I've changed my ways by becoming less clumsy.
I’ve been overwhelmed with all the information, and have met with 3 pharmacists, a physiotherapist, an endocrinologist, a dentist, and decided no drugs or hormones for now. Just improved diet and exercise...And tracking everything...
I’m meeting with my GP next month to arrange more in depth tests.
Have a great weekend☀️
Thank you. I hope your doses continue to go well.
Guess I'd better up my game!! I'm 66 and don't walk nearly as much as you do. You've motivated me to shoot for 10,000 steps.
My suggestion is to get a doctor team which will provide you with the support you are needing! Some people have no side effects. I was not that lucky. However, there are ways to avoid the side effects (like longer infusions, titrating up slowly) a GOOD team is ubber important! I am tolerant of the risk because 7 women I know, fell last winter and ALL broke or fractured bones! That really take you down. You don't heal easily and your muscles atrophy in the process. My advice is to just DO IT - you can always stop or change meds. Some people can't take them later. They also can't have surgery later. So its best to get it out of the way as early as possible. I am on Reclast and Tymlos - a total of 5 years and then I am done for life. I already have GOOD trending numbers in my second year. My bones unexpectedly fell apart in surgery (C5). The Dexa's without the TBS software are not reliable sometimes. I'll take my medicine like a good girl!