Does anyone have a solution to help manage Reclast side effects?
Does anyone have a solution to combat Reclast side effects. I had the infusion a year and a half ago and the side effects started shortly after I had the infusion. I still have weak legs, swelling in feet, pain in bones, dizziness (serious dizziness), cold sweats, tired all the time and nervous twitching in bones. Any suggestions?
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I've only had one because my former QUACK DR said I had Osteoporosis, when indeed, I had OSTEOPENIA!
I have all sorts of side effects from it!
I will NEVER take it again!
To me, it's POISON!
I will NEVER put this POISON in my body again! Between CHRONIC hives, exhaustion, bone & joint pain, no way will I allow this in my body!
PLUS, my then "Quack Dr" misread my DEXA scan! I have had Osteopenia for over 15 yrs & still do, according to my new Dr who showed me the results!
He diagnosed me with SEVERE OSTEOPOROSIS!
I turned him in to the medical board, which was a TOTAL waste of time! Of course the Medical Board & CDC are going to side with "BIG PHARMA!"
All doctors seem to push bone drugs. Could all our bones be ready disintegrate and collapse on us someday? Now i am taking prednisone and that makes bones weak. Feel like i can’t win.
Yes, we can ignore till there are actually broken bones, then it makes the osteoporosis real
I am so sorry about your dreadful side effects. And it's not your fault as drs do not tell us enough information or they are ignorant. I am trying to decide what drug to take after coming off Prolia. They are all poisonous.
How do these drug companies get a licence? In America the drug companies pay 60% to the FDA. In the UK it's 80% subsidised by the companies. I am trying to find out what percentage they pay our Australian Licencing Authority.
Do look up Dr Aseem Molhotra. He has become an activist against these drug companies. Brave man!!
I have seen people lose their quality of life and die a painful death from osteoporosis. In my family is genetic. I have lived my life trying to prevent it, with no luck. My sister has as well. We are so glad we live in a time when there is medication to help it. I wish I started it sooner, but I thought I could do more and more to prevent it. I couldn’t. I wish people understood that sometimes you can not do anything, and it is simply genetic.
Thanks to the link to Molhotra, Victor.
I’m having the same issue. Aetna has one pathway to Evenity - must fail Prolia. Prolia is not an option medically.
I am 75 and I have osteoporosis of the lower spine. It's not always genetic I'm the only one in the family of 12 that have it.
I know it’s not always genetic. There are many causes for it, as Dr McCormick explained to me. I had Lyme disease for a long time and that could have contributed. As well as being 100 pounds most of our lives. But my dad was 170 pounds, so that didn’t contribute. It is great we have medical interventions for those of us who did everything right, but still ended up with osteoporosis. I know someone who could even ride in a car because going over a bump would cause a painful fracture. We are so fortunate these days, and, I expect, it will only get better for future generations.