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STATINS ARE POISON…Get your loved one off of them!
PART TWO: Statins speed up the transition from "midlife vigor" to "debilitated old age'. Every cell in your body needs cholesterol!
Statin side effects mimic the effects of aging; they include fatigue, weakness, instability, memory loss, reduced mental capacity, dementia, neuropathy. slowed reactions, muscle atrophy (wasting), muscle pain, Myopathy, Rhabdomyolysis, Kidney failure, dyspnea(difficult or labored breathing) and heart failure, heart conditions, intestinal disease, pancreatic problems, diabetes, cataracts, nerve damage, reduced libido, depression, accidents, suicide and cancer…also linked to ALS Lou Gehrig's Disease and early onset Parkisons.
Every cell in our body needs cholesterol.
Recently scientists have found that statins interfere with our stem cells, which work to repair damage to our bodies and protect us from muscle and joint pain as well as memory loss.
A study from Tulane University found that statins prevented stem cells from performing their main functions, namely reproducing and replicating other cells in the body to carry out repairs; in particular, statins prevented stem cells from generating new bone and cartilage.3
According to Professor Reza Izadpanah, a stem cell biologist and lead author of the research, “Our study shows statins may speed up the aging process. . . People who use statins as a preventative medicine for health should think again as our research shows they may have general unwanted effects on the body which could include muscle pain, nerve problems and joint problems.”4
And to what purpose? The twenty-year Honolulu Heart Program study compared changes in cholesterol concentrations over twenty years with all-cause mortality. It found that those individuals who had low cholesterol levels were at increased risk of death.
Physicians’ Experiences as Patients with Statin Side Effects: A Case Series:
This is the first analysis to address the experience of physicians themselves affected by adverse effects (AEs) of statin medications, encompassing muscle, neuropathic, cognitive, and behavioral AEs.
The impact of statin AEs in physicians can be profound, professionally and personally, in some cases requiring major professional modification or early retirement.
Poor awareness of statin problems by medical providers, and low receptiveness to reports of such problems, can extend even to patients when they themselves are physicians.
Patient A: Atorvastatin 40 then 80 mg was followed by cognitive problems, neuropathy, and glucose intolerance in a Radiologist in his 50s
Patient B: Atorvastatin 10 mg was followed in 2 months by muscle weakness and myalgia in an Internist in his 40s
Patient C: Atorvastatin, ezetimibe/simvastatin, rosuvastatin at varying doses was followed shortly after by irritability, myalgia, and fatigue in a Cardiac Surgeon in his 40s
Patient Simvastatin 20 then 40 mg was followed in 4 years by mitochondriopathy, myopathy, neuropathy, and exercise intolerance in an Emergency Medicine physician in his 50s
Patient E: Simvastatin 20 mg and niacin 1000 mg was followed in one month by muscle weakness and myalgia in a Physical Medicine and Rehabilitation physician in his 50s
Patient F: Lovastatin 20 mg then simvastatin 20 mg, atorvastatin 20 mg, rosuvastatin 5 mg, niacin 20 mg and ezetimbe 10 mg was followed by muscle weakness and myalgia in an Obstetrician/Gynecologist in his 70s
Patient G: Ezetimibe/simvastatin and atorvastatin (dose unavailable) was followed shortly after by cognitive problems in a Radiologist in her 80s (probable causality).