Antioxidants: draxe.com/top-10-high-antio... - Cure Parkinson's
Antioxidants
Thanks, Mill! I unsubscribed some time ago as I was receiving a lot of promotional emails. Any way, clove oil and dark chocolate must be in everyone's antioxidant list.
Take a Q-tip and soak it with clove oil then rub the roof of your mouth and swap the tongue as well. It's an excellent anti-salivation remedy.
Dark chocolate is included in our breakfast every day, or snack on it any time of the day.
Hi Despe. The reason I m looking at antioxidants is because after coming across Jaberalhd’s posts and how he beat PD I was looking into Xanthohumol (XN)98%. It is supposed to be powerful antioxidant but the problem is that it has estrogen effect which can be dangerous. Researching further, it seems there’s tetrahydroxanthohumol (TXN) that has been manufactured from XN does not have the estrogen effect but then it is not as powerful as an antioxidant.
I asked Patk Bear if he could locate Jaberalhd’s posts but he could not. His posts appeared when I was scrolling and reading. He is from UAE and suffered tremendously and I felt very happy for him following his journey when in his last posts he thanked Silvestro and Park bear for their help as he had recovered and was better than 5 years ago. I made a post asking if anyone was taking Xanthohumol 98% and a screenshot of his posting detailing what he took.
It seems Xanthohumol is the natural alternative to NILOTIBIT
I m not so tech savvy so I didn’t know how to post his actual post
Mill,
Before your post, I had never heard of this substance or the individual. Didn't have a chance to search it yet.
Despe, I have found his post. How do I repost it on HU? It’s really important for everyone
I found his post when I searched nilotinib
Mill, highlight the link at the very top of your screen using your mouse. Right click the mouse, you will see "copy," highlight "copy." On the page you want to post it, place your mouse in the body of the page, right click your mouse again and you will see "paste." Paste it on the page and you will see the link. Hope it helps.
It takes a lot more than fancy charts and colourful pictures of food to convince me that the whole anti-oxidant thing is important. It reeks of pseudoscience..
Much better to eat whatever you like - possibly with some fibre.
To each their own. The take away from this study is to drink beer in moderation (organic of course).
Here's an interesting study of high dose antioxidant melatonin. There is now a clinical trial of different delivery methods of hd melatonin but its a large PDF and I don't know how to link it. It's at the top of the Google search for hd melatonin.
Our collective brain power can do amazing work. Thanks for sharing.
I didn't read Jaberalhd’s testimony yet. I first wanted to understand the effects of nilotinib, it is a chemotherapeutic drug for leukemia that is now being investigated for use in PD.
Paraneoplastic syndrome produces neurological symptoms. It's possible that this was the underlying cause of Jaberalhd’s disorder and it would be hard to know without blood tests.
Cancer and Neurological disorders are on a spectrum. I speculate that neurological diseases are in fact autoimmune disease and a variant form of cancer. Rather than turn to pharmaceutical drugs it would be prudent to turn to functional nutrition such as antioxidants.
My initial dx was Parkinsonism with tremors (thought to be MSA-C) and changed to ALS-Plus last year. I found a research study that suggests ALS is a paraneoplastic disease, this makes sense to me because ALS is linked to non-hodgkin lymphoma. Parkinson's disease and Amyotrophic Lateral Sclerosis are both disorders of the serotonergic system, and are more closely linked than people realize.
What might happen if we treated neurological injury as though it was blood cancer with functional medicine? That's my plan forward.
ncbi.nlm.nih.gov/m/pubmed/2...
I think he was dx with PD. Read his post and take what you need from it. Cheers
Are tremors MSA and ALS symptoms? Thank you.
Yes, but they are not the resting tremor you see in PD.
ncbi.nlm.nih.gov/m/pubmed/2...
onlinelibrary.wiley.com/doi...
Thank you. The differences are distinct.
Hi Millbrook! I was interested in jaberalhd’s post when he initially wrote it I received a brief reply when I private messaged him, I will see if I can somehow share it, I’m not tech savvy at all.
Connie
Connie,
for you his post.
Hi I am new her but not new to Parkinson’s ,I was diagnosed 7 years back but I was suffering from symptoms many years before that .
In my country United Arab Emirates the vast majority of people doesn’t know much about PD they think it’s a little bit of shaking which is not a big deal , my friends , coworkers and family think that I am pretending sickness because sometimes they see me doing fine when I take my medications.
I don’t want to bother you with my story and to make it short I tried to manage PD and cure myself in every possible way.
I experimented almost everything came to my knowledge and mind including supplements except DBS and spent a lot of money for that almost all my savings.
I did stem cells, Ayurveda, herbal medicine, energy therapy, Chinese medicine, acupuncture, Nilotinib and ext.
But lately I think I got some positive response from my experiments.
I reduced my medication to the half, and they are working for longer periods, my dyskinesia improved my sleep is better and I can drive again my facial expirations is normal, my cognitive and memory are much better and still improving many thanks to silvestrov posts on this forum and others .
I am taking now only:
450Mg Sentiment every day divided into 3 times (250+25Mg one time and 2 times 100+25mg)
Neupro patches 6mg
Supplement
Xanthahumol morning only
Baicalin before sleeping only.
Glutathione Nebulizer
Drinks
Green Barely juice
Trevo fruit drink
Bravo! Please tell me where you found the glutathione nebulizer.
Connie was interested in jaberalhd’s post. I just sent her his post. Sorry...
