disappointing results: would you continue or skip 2nd year of tymlos?
From what I've read, year 1 is usually one's best results on Tymlos, with 2nd year not as productive. I just got my DXA after 1 year on Tymlos and it's somewhat disappointing. a 5% gain in spine, no gains in hip or femur neck. Still firmly in osteoporosis land.
Tymlos is costing me a lot of money, as the Radius savings card runs out midway thru year. I'm wondering if a 2nd year is even worth it, if most gains are in year 1?
Seeing doc soon to discuss, but feeling discouraged. (I don't smoke or drink alcohol, maintain a good diet (no added sugar or salt, plenty of healthy veggies and proteins, very little red meat) get plenty of calcium, Vitamin D3, K2 and do weight training and weight bearing cardio daily. I don't think there's much more I can do.) 🙁
Interested in more discussions like this? Go to the Osteoporosis & Bone Health Support Group.
Thanks for chiming in YMV - really appreciate you sharing your experience.
No bone markers were done, so just going by the DXA. You wisely asked the same "what's next" as others - and my reply is "um - I'm not sure!"
Maybe exploring switch to Forteo (I tolerate meds well so switching may not cause problems.) But I'm already approved for Tymlos: not sure if I'd be approved by my insurance to switch or if it would be a hassle to get reauthorized. (I'm on employer insurance.)
Or maybe give Tymlos 6 more months - based upon what windyshores and mayblin have mentioned. At worst, I'd hopefully maintain vs lose more.
Read “Good Bones”.
From what I've read, on the contrary, t has more effects on hip than f. The two drugs are so similar in many ways, personally I don't see a lot advantages switching from t to f, especially at the stage you are in. See if others can chime in with regards to this take. As far as follow up with evenity, follow windyshore as she is a pioneer with this combo sequence. And, of course, consult with your team of physicians.
Tbs provides a bit insight to the 'quality' of one's bone, though I haven't read too much into it yet and not sure how it relates to true bone quality. Mine improved to lower end of normal, but i still have op. How does this make sense? Nonetheless, it provides some info to us. Yea Google it and see where yours land.
This is from pdr.net (physicians desk reference):
"Romosozumab is also a treatment option for patients previously treated with teriparatide or abaloparatide."
Both Forteo and Tymlos are believed to work by a very similar mechanism. I would guess that if you want to see bigger gains you might try Evenity as it does work by a completely different mechanism. I tend to think switching to Forteo would be like continuing Tymlos for the 2nd year. "Teriparatide (brand name Forteo) and abaloparatide (brand name Tymlos) are medications used to treat osteoporosis. Forteo is a lab-made version of human parathyroid hormone (PTH) and Tymlos is a version of human parathyroid hormone-protein. These two drugs are both similar to the PTH that your body produces naturally."
And yet you never know for sure, even though Tymlos and Forteo are similar you might get a different and improved response to Forteo.
BTW in terms of benefiting the hip my memory of different reporting on the three anabolics is that Forteo tends to have the least benefit for the hip (and forearm) with Tymlos slightly better and Evenity better still.
Sorry you didn't get 10-15% improvement and best of luck on whatever you do next.
yes, I seem to be.
Yippee!! Great news! Very happy for you! I know it’s all individualized, but would you mind sharing what your doses are?
thank you! yes, everyone reacts differently but the .025 transdermal dose (the lowest dose) is supposed to have bone-maintainence effects. I've been on that for 5 years. I just increased my dose to .037, the next available dose. Still a very low dose but perhaps will have a slightly greater impact and I was hoping it would help with sleep. No luck there though.
Do you use transdermal Estradiol or Estriol or a mix? I’m using mix, but having fluid retention. I increased Progesterone to 100mg. hoping for help with sleep, but as you said, no luck.
All these 17 updates of today were very useful me.
Since Sept 2022, I have been on Tymlos. I did a DEXA after a year and radiology report description) said significant increase. (I wish I had insisted my endo doc that she views actual DEXA scan. If I were an endo practioner, I would have done that automatically.)
My endo doc has retired and I have a new endo doc who did review my med and bone history with me. She is willing to prescribe me tests of my choosing. After being on this support group, I see value in doing TBS and PINp and may be CTX. (I haven't checked for cost coverage of these tests. My medical insurance probably would cover these.)
She suggested that after 2 years of Tymlos, I would be a candidate for 70 mg/wk Fosamax or annual infusion type bone-building med. (For 10+ years, I was on Fosamax but discontinued as my Osteopenia was stable; may be a mistake on my part.)
I would welcome further discussion on my comment.