The following consolidates several previously written articles on Parkinson’s Disease, and the possible strategies for attenuation of symptoms and a possible complete remission of this debilitating condition.
In this Substack’s ongoing anecdotal repurposed compound crowdsourcing series comes another absolutely incredible healing experience.
The first success story further corroborates this Substack’s recent article on Ivermectin curing various neurological conditions…
NEW ARTICLE: IVERMECTIN and FENBENDAZOLE Testimonial - 78 year old Nebraska PARKINSON’S DISEASE patient of 8 years, cured after 4 months!
My best Parkinson’s Disease & Ivermectin testimonial yet!
77 year old Nebraska Parkinson’s Disease patient of 8 years
From patient’s daughter: “He has been on the protocol you gave him for four months”
“Today he went to the neurologist...and unbelievably the doctor told my dad that he is questioning if my dad even has Parkinson’s anymore...he told my dad he looks healthier than he’s ever looked!”“He doesn’t shuffle or slump over like he used to and his shakes are minimal!!! My dad was just speechless!”
I run the world’s largest Ivermectin Cancer Clinic.
At the end of this article there will be a synergistic protocol which may more potently treat all of the various diseases featured in the following article:
The latest research now strongly suggests that Ivermectin may not only cure Alzheimer’s Disease, Parkinson’s Disease, turbo cancers, viral infections, and many other ailments, but it can also serve as a powerful antidepressant that increases the production of dopamine; to wit:
Conclusion
This study provides novel information about the effects of IVM on DA release in slice. Dopamine release in the striatum is mediated by many intrinsic factors, including ion channels, autoreceptors and heteroreceptors. Through FSCV experiments, IVM is increasing DA release independent of P2X4 receptor activity in the DS, even though P2X4 receptors are in this region on microglia as well as other cells. Ivermectin also attenuates nicotine effects as a high-pass filter in a way that is not mediated through P2X4 receptors. In addition, IVM is able to increase CIN firing rate frequency, highlighting a possible mechanism through which IVM is acting to affect DA release. With that, HEX was used to block CIN outputs on nAChRs and saw that IVM no longer was able to increase DA release. Ivermectin was also unable to block HEX as a high-pass filter, suggesting that IVM is affecting DA release directly through nAChRs, providing further evidence of IVM acting on DA release through CINs. And when IVM was co-applied with L-DOPA there was an even greater increase of DA release compared to IVM or L-DOPA alone. In addition, co-application of L-DOPA with IVM saw a decrease in the normalized 5 pulse ratio, showing that L-DOPA and IVM together is decreasing the readily releasable pool of DA, meaning that IVM is acting through a different mechanism then L-DOPA. This study has helped elucidate the effects of IVM on DA release and how it is able to mediate the cholinergic system in the DS.
Unpacking this conclusion, CIN stands for cholinergic interneurons which are crucial for normal motor and behavioral functions of the basal ganglia. CINs function in a kind of pulsed firing, or pause-burst sequences, with pauses being responses to motivationally significant events; in other words, motivationally significant stimuli cause CIN’s to pause firing, and Ivermectin accelerates the CIN pause-burst rates such that there is an increase in dopamine release.
Increases in dopamine release, along with attenuation of fungal brain infections and prevention of the formation of the infectious form of the prion protein in prion-infected cells, may be the contributing factors to curing Alzheimer’s Disease, as well as Parkinson’s Disease, depression, ADHD, etc. & etc. & etc.
And because according to the research study, Ivermectin effects are mostly through DA terminal excitation and not through additional changes in vesicular content, this miracle compound may very well be a powerful dopamine releasing agent, which could also serve to help with drug addiction and dopamine dysregulation syndrome, whereby Ivermectin recalibrates the “reward center.” Since dopamine is critical for many body functions, including memory, movement, motivation, mood, attention and more, and since high or low dopamine levels are associated with diseases like Parkinson’s disease, restless legs syndrome and attention deficit hyperactivity disorder (ADHD), we may conclude that Ivermectin, with a safety profile that is far superior to aspirin, should be strongly considered as a novel repurposed drug therapy for these conditions.
The combination of Ivermectin, Fenbendazole, nutraceuticals like ImmunX and compounds such as low dose lithium orotate along with a high fat ketogenic diet underscores the importance of repurposing existing drugs and natural compounds in order to create highly accessible new treatment paradigms for neurodegenerative diseases, and even mood disorders.
The Ultimate Dementia, Alzheimer’s & Parkinson’s Disease Cure Protocol
Fenbendazole 150mg every other day with dinner for 30 days, and repeat every 4 months
Ivermectin 12mg every evening with dinner indefinitely
Low dose lithium orotate 4.8mg capsule in the morning with breakfast and in the evening with dinner indefinitely
ImmunX immune support 2 capsules in the morning with breakfast indefinitely (Quercetin is a critical ingredient in ImmunX, and as per research studies similar to Ivermectin it displayed capabilities against tauopathy by inhibiting the hyperphosphorylation of the tau protein, thus its anti-prion activity helps to reverse Alzheimer’s Disease)
Removal of sugars and carbohydrates, with an emphasis on a modified ketogenic diet consisting of high quality fats like eggs and avocados while replacing table sugar with a zero glycemic index, zero calorie, keto friendly rare sugar like AlluX
Methyl B-121 x 1,000mcg daily on empty stomach (water-soluble vitamins are better absorbed without food interference [given that AD patients have been shown to have severe vitamin B-12 decencies])
Do NOT comply.
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If symptomatic people and healthcare providers only knew .
Wish we had known about these treatments long ago! My dad had Parkinson's and my husband and mother had dementia.