REVERSING PARKINSON'S DISEASE

[crewmanwhite]

Dr George Ackerman, founder of Together For Sharon, a Parkinson’s awareness organisation, was gracious enough to interview me for his podcast.

In a short time, we covered many topics including strategies to help us recover our health when diagnosed with Parkinson’s, my own story of recovery, and why mainstream Parkinson’s organisations won’t support research into recovery protocols or those who develop them.

Please forgive the untidy background and my less-than-formal attire, but I thought it was intended as a voice only broadcast. It was also very early morning, so I am chugging down Rooibos tea to give me the energy to chat with George.

Despite my looks and sleepiness, I hope you enjoy our conversation.

youtube.com/watch?v=UPy01lG...(Not working as expected?)

[JayPwP]

Don't worry... We are messier than you...

[Hope-full1970]

Thank you for sharing this encouraging message. I have been on a recovery journey and am working on removing toxins. We need all the encouragement we can get. It's too easy to get discouraged in the journey. A positive message is always appreciated!

[oksadavlatte in reply to Hope-full1970]

My mom has been on generic Sinemet for 8 weeks, and her improvement is remarkable. She's 86, and until the last 18 months, she had never taken any medication and was energetic and bubbly. She had a dramatic and fast onset of Parkinson's, and prior to starting this medication, she was almost completely debilitated. She looked like she was slowly dying. She lost a lot of weight, was shuffling, stooped in posture, exhausted, and confused. She now takes 1 tablet three times a day (25/100). Zero side effects. And, now, two months into this, she's 75% back! It's a miracle

[Hope-full1970 in reply to oksadavlatte]

I'm so happy it is working for her! At her age you really don't have to worry how long she'll be on it.Sometimes it doesn't work as well for other people. I'm glad it's helping her the quality of life!

[crewmanwhite in reply to oksadavlatte]

Levodopa drugs can be wonderful for improving quality of life.

However, it is important to keep the doses as low as possible to minimise adverse effects, plus she needs activated folate or folinic acid each day to prevent accumulation of homocysteine. Vitamin C will help the levodopa work better if taken at the same time.

[Esperanto in reply to crewmanwhite]

The interplay between levodopa, homocysteine, and B vitamins is complex, necessitating a more nuanced approach to supplementation. Simply supplementing with one or more of these B vitamins could potentially lead to other imbalances or even interfere with the efficacy of levodopa treatment. For instance, high doses of folic acid can mask a vitamin B12 deficiency, which may result in neurological complications. Therefore, an upper limit (UL) is recommended, depending on age and gender, ranging from 400 to 1000 mcg, which applies to all forms of supplemental folate, including activated forms.

PWP should have their homocysteine and B vitamin levels (B6, B12, folate) monitored regularly. Supplementation should only be tailored if deficiencies in B vitamins are identified.

[crewmanwhite in reply to Esperanto]

All supplementation should be monitored by a qualified practitioner, but often is not (and doctors are not qualified in this area).

In my 28 years of practice, I have never seen an adverse effect from supplementing with up to 1000 mcg activated folate in patients taking levodopa drugs.

[Esperanto in reply to crewmanwhite]

You did not mention the upper limit (UL) for supplemental folate, even though exceeding this limit could mask a B12 deficiency. Additionally, your anecdotal claim is misleading because it implies that no adverse effects ever occur below this limit, which isn't entirely accurate, particularly in the specific context of PD and levodopa use. While 1000 mcg of activated folate may be tolerated by many, it does not guarantee the absence of any interactions or subtle effects, especially in the long term.

[LAJ12345]

really encouraging video

[BadgerBruce]

Thank you for this encouraging talk I was diagnosed with early onset Parkinsons 2 years ago and want to fight this darn disease and at the very least slow progression. Thanks for the inspiration

[Meg024]

Thanks for sharing hope. I have digested John Coleman's books and they mean a lot to me. I have chelated mercury with ALA for 100 rounds and take only 440 mg levodopa per day. I do about 50 min of exercise a day and lead a quiet life with creative pursuits. I could never be as determined and hard-working as John Coleman, but we are all different.

[DogsWoode]

I thought this just a WONDERFUL inspired message. Is this possible? Can I do it? Can I change my attitude from the 85% to the 15%. I had no idea this could be possible, THANK you!!

[Hope-full1970 in reply to DogsWoode]

Yes you can!!

[DogsWoode in reply to Hope-full1970]

Thank you thank you Hope-full. 💕

[JPeezy]

Wonderful interview! I am curious about your mention of stealth infection like bartonella and mycoplasma pneumonia (add in Lyme’s, EBV and strep, living in mold). Do you think these infections mimic Parkinsons or are the root cause? Curious bc I have all of those.

[Hope-full1970 in reply to JPeezy]

I have had Bartonella and EBV. Bartonella can absolutely mimic Parkinsons. The key is finding a Dr.who understands that. I have been fully treated and I am still left with my issues so it was part of the issue but not the whole issue. I had my well water tested and it was high in Uranium and manganese. Manganese toxicity can mimic Parkinsons. We just had a treatment system put in.My Dr. is treating me for covid shot injury since all of this came on after the shot. Now I have all my answers and I would think if I eliminate all my underlying issues and toxicity I will be able to see if I can push back, reverse or eliminate symptoms.

[Shack2023 in reply to Hope-full1970]

Hi can you let me know the protocol you are following for Covid shot injury? Thank you

[crewmanwhite in reply to Shack2023]

As I chose to avoid all alleged vaccines for the alleged pandemic, I have not experienced any of those challenges.

[Shack2023 in reply to crewmanwhite]

Thanks I was hoping hope full 1970 could share protocol mentioned above

[Hope-full1970 in reply to Shack2023]

Hi! Yes, gladly. The first thing my Dr. put me on was Ivermectrin 20mg.He added Nattokinase(Allergy Research group)to help bind the spike protein.

He also added Black Cumin Seed Oil(Life Extension)

Along with NAC (Augmentata)

All of these can be bought over the counter except Ivermectrin

They all help with Nueroinflammation and help bind and remove spike protein.

You can try 1 at a time for a week to see how you react. I have had a good reaction to all of these.

The Nicotine patch works. I tried it once and didn't see much of a difference but everyone is different.

Lastly I'm on CBG ,it has no THC. It also helps to destroy spike protein and heal and balance nerve receptors.

I started this process 5 months ago with a DO who also gives me craniosacral therapy.

[Shack2023 in reply to Hope-full1970]

Thank you

[crewmanwhite in reply to JPeezy]

Parkinson's is a group of symptoms with a variety of causes. Stealth infections are one group of causes and are usually accompanied by toxins and stress.

So we need to treat the infections, toxins and stress rather than this nebulous "disease" we call Parkinson's.

[cceelen]

great post, thank you!