Statin Induced muscle pain and stiffness

Unfortunately I tried Repatha and couldn't do that one which is why the Praluent. However since my knee replacement it's been difficult and I'm two years out on the replacement.

I can see the posts are all over the place with Co-Q-10 and Statins.

Every study will have another study done which contradicts the other. I chose to listen to my doctors at Mayo Clinic. My heart failure doctor is the Director on heart failure/transplant division and far more knowledgeable and experienced than anyone on MCC.

My PCP who does research before recommending anything is also a trusted person with decade of medical expereince.

I think most posters will agree that everyone is different. What one medication or supplement works for one person it may not work for you or others. The same goes for side affects in what one will have another will not.

My opinion and not medical opinion is if medical professional asked you to try something to treat a medical condition try it and if you have problems talk to your medical professionals about different things to try. If a medical professional asked you to try a supplement to help alleviate a side affect try it and again if does not work talk to them and see about others things you can do including changing medications.

I say the above based on the experience and expertise of Mayo doctors and have not idea of the experince and expertise of other posters doctors and specialists. So yes I trust my medical professionals at Mayo but maybe you don't have medical prosfessionals with same degree of medical expertise and experience as I have with being a Mayo patient.

Hi JC - In principle, I agree wholeheartedly.
You may notice that the Mentors and Moderators often step into discussions and suggest that the poster consult their provider.

But...
Not everyone can get into Mayo - their care is a limited resource
Not all providers are accessible or can/will take the time to explain
Some of us do not have choices and cannot get a trusted doctor of our choice - the "medical desert" is real - friends in rural Michigan have access to one NP one hour away - specialty care is three hours away and takes months to get in.
Some have insurance that limits their choice of/access to providers
20% of people in the US have no medical insurance
Some of us have rare conditions, for which we don't have ready access to knowledgeable specialists. We use MCC to educate ourselves, and then hopefully our providers or to help us find new providers.
Some just want to hear from others who are walking their same path.

I had a trusted and beloved PCP who was pushed out of primary care because the company demanded immense caseloads. That was over two years ago and I have literally tried 6 other PCP's since then, and am about to ask to be accepted by a seventh. Several of those I tried just aren't knowledgeable enough for my older body with many issues, others were only willing to "go with the script" and one looked like he just rolled out of bed and put his lab coat on over his sweats and came to work without combing his hair. It has been humbling to go through what many of our members do and feel powerless to get to the right provider.