I have been experiencing hand tremors in one hand for a couple of years. My handwriting was terrible as a result of these tremors. So I made a list of my little aches and pains and went to an acupuncturist as an experiment. I knew this wasn't parkinson's, but when I returned home, my tremor was gone. I did a little research today to find some interesting articles. It attacks parkinson's in several ways, so I suggest anyone with the disease do a little research.
I'm treating my Parkinson's disease with herbals, exercise, & have chosen TCM ACUPUNCTURE (Traditional Chinese Medicine) over traditional DBS;
After 4 treatments, I can now FAST WALK a block without the walker.
I also added Calcium Edonite Clay to detox from a plant-sourced Vit C which contains "ESSENTIAL TRACE ELEMENTS"--unlike my usual fastidiousness in Research, I 'paid no mind' to what the TRACE ELEMENTS are! I progressed rapidly with ~ 4 months use: TRACE MINERAL ELEMENTS, aka: UDOMS ARE DEADLY FOR P.D. PATIENTS!! ANCIENT HEAVY METALS washed up from the sea!!! Just what P.D. does NOT WANT! Within 3 days of detox (metals, pollutants, herbicides & Pesticides, fluoride from tap water treatment, etc).
Note: I called the Nat'l Parkinsons Foundation: rep said she had never heard of any detox!!
Just a plug for my favorite help regarding Parkinson's Disease. I have found in at least three cases I know of personally, that the use of AEP has slowed or stopped the progress of the disease. Please take a look at the on line article by googling, "Nutrition Review... Calcium AEP Membrane Integrity Factor" which talks of the many benefits of AEP. Lately AEP has also been shown to help PD. AEP can be found on line but I rarely can find it in health food stores. I first saw the benefits from reading Dr. Adkins' book, Vita Nutrients. He used it in IV form with his MS patients. I get mine from Wellness Resources.
My mother was prescribed too much Carbidopa / Levodopa a.k.a. Sinemet at the outset of her Parkinson's diagnosis and she developed an allergic reaction to it that resulted in terrible rashes with debilitating itchy hives all over her body.
After many efforts to find solutions, my sister solved the allergy by having her take Benserazide / Levodopa a.k.a. Madopar [sold in Europe], which cleared up the rashes while preserving the long-term benefits of a parkinson's medication.
Sometimes a slightly different take on a conventional approach can make a huge difference.
I have been hearing a lot lately about cholesterol lowering drugs, and the link to alzhiemers . Don't you think, it could also be a factor in Parkinsons disease??? The brain is mostly cholesterol anyway. Not sure, but in 80-90% range. I would bet a lot of Parkinsons patients take these drugs. Just a theory. God Bless all who are looking for answers and Help. He has never failed to help me.
I'd urge everyone to look into CoQ10. This research study gave 1200mg of CoQ10 per day to those with early Parkinson's and showed evidence of slowing functional decline: https://www.ncbi.nlm.nih.gov/pubmed/12374491
If you've never heard of Howard Shifke and his site Fighting Parkinson's Drug Free, I recommend you visit it.
I have recently been diagnosed with Parkinson's. Has anyone used the HP therapy successfully with PD. Another site claims success with it, but before jumping in I wanted to hear from someone that had used or is using it successfully.
Hello, Does anyone have any experience with magnetic field therapy and Parkinson's disease?
(Denver, Co, Usa)
I believe Malassezia yeast may be the actual/most common cause of Parkinson's, in combination with environmental & virulence factors that favor its growth and aggressiveness. If so, this has definite implications for prevention & treatment.
Consider the following points:
(a) Malassezia is an unusual yeast in that it is lipophilic (meaning it feeds on lipids rather than sugars/starches like candida). AND it seeks melanin & infects melanocytes. The dopaminergic neurons in the brain -- the area affected by PD -- contains high levels of neuromelanin. Neuromelanin in turn has an affinity for lipids and for iron, both of which favor the growth of this yeast. Note: because it feeds on lipids rather than sugars, it will NOT grow in the usual fungal cultures performed in hospitals (they use sugar/starches in the medium, no lipids). So it is "under the radar" in the sense that there seems to be little testing ever done for it.
(b) Malassezia is known to infect melanocytes in the skin... and I suspect it is involved in causing skin cancer. If so, this would explain the higher rate of skin cancer found in Parkinson's. Also, because it is in the skin (IN, not only "on"), it could hypothetically be pushed into the bloodstream or spinal fluid by medical procedures like injections or spinal taps.
(c) L-DOPA is a precursor to MELANIN, so it makes sense that Malassezia might take it up ... thereby reducing the amount available for normal brain functioning. Low L-DOPA is a key feature of PD.
(d) Acetaldehyde -- produced by yeast -- converts dopamine into a neurotoxin called salsalinol ... which may cause the eventual aptosis of dopaminergic neurons. It also promotes increased iron content and the release of iron, both of which would favor fungal growth.
(e) Malassezia is extremely common and extremely slow-growing. It may be that people have it for decades or a lifetime. I speculate that risk factors for developing PD might include: prolonged use of antibiotics (esp. intravenous) or steroids/immunosuppressants, depleted flora from any other source including packaged foods which contain additives or may be irradiated to remove flora, accumulative lifetime exposure to UV radiation, including sunlight, medical procedures like CT scans et al; eating a lot of oleic acid (vegetable oils including olive oil are the primary culprit here, but also animal fats), high cholesterol/triglycerides, PRN lipid therapy, taking Vit D or iron, use of certain psych meds like antipsychotics that increase lipids. Meds that cause photosensitivity (= less resistance to UV radiation) might be another area of concern.
If my hypothesis is correct, there are definite implications for prevention steps and maybe also treatment. Some possibilities that come to mind are increasing dietary sulfur (antifungal), increasing "good" flora, avoidance of risk factors including dietary veg. oil/animal fat, etc. Based on my reading, buckwheat also contains an antifungal compound. Whether such steps would have an effect, I don't know. More research is clearly needed.
For those who may remember, I have previously reported the benefits of high dose vitamin B-1 /Thiamine HCL for Parkinson's disease.
Now I would like to talk about one of my favorite supplements, melatonin, that a recent randomized, double-blind, placebo-controlled study showed was beneficial for PD patients after just 12 weeks of supplementing only 10 milligrams per night! Yes, finally, a quality human study confirming that melatonin is beneficial for people with PD.
This study showed multiple benefits in patients that include the following. Using standard testing, melatonin showed improvement in anxiety, depression, total antioxidant capacity, increased glutathione, and improved UPDRS Part 1 test results! Melatonin also significantly lowered the inflammatory marker, hs-CRP, or high sensitivity C-Reactive Protein and inflammatory TNF-a while lowering LDL cholesterol and improving insulin resistance! Some of these improvements are suggestive of the idea that a more extensive study and or higher dosing may produce even better results because many of these improvements imply a reduction in total oxidative stress and oxidative stress is one of the most damaging factors in PD that destroys dopaminergic neurons and other cells in the substantia nigra of the brain.
To say I am excited that this study would be an understatement! Studies showing benefits like these in humans with PD from a single supplement are almost non-existent. Hopefully, they will follow through on this study with similar studies using pharmacological dosing of melatonin and more extended length studies.
While this study is very good and confirmed that melatonin can be beneficial in people with PD, it leaves many unanswered questions such as what would have happened if the study had been 24 weeks long instead of 12 as 12 weeks is very short for a study like this? Would the benefits range increase, would the benefits stay the same or increase the level of improvement seen? What would have happened at higher dosing?
Remember that Dr. Shallenberger is using dosing that is as much as 36 times higher than what was used in this study in some of his patients, and he gives all of his patients 180 mg of melatonin per night in the form of three 60 mg capsules in the evening. He considers this a preventative dose.
Overall, I feel this study has opened a door that has been closed for too long, and hopefully, there will be follow up studies to answer these questions! Here is a link to that very recent study abstract :
To Whom It May Concern,
I have a mother who is in her early 70's and has been diagnosed with Parkinson's. She fell ill with a h-pylori infection and almost died. The ER doctor put her on some strong anti biotics and she is recovering from the pylori but when we took her in she was shuffling badly, slight arm tremors and a mask like face. I've tried to get her to eat better, avoiding foods with lots of sugar, pesticides etc but she's used to her diet and is struggling. Regardless of this she has still shown signs of improvement but is complaining of weakness, stiffness and a feeling that she can't move at times when she wants to. I have read through the threads on this site about the Methylene Blue. I cannot understand the dilution. I have no way to since I am dyslexic with numbers. I have personally been taking the MB 1% diluted by taking one tspn full of MB and diluting it with 9 tspns of water. I take 5 -7 drops in the morning in 6 ounces of water with a 1/4 tspn of vit c powder and a 1/2 tspn of baking soda, sometimes a full tspn.
My questions are:
1. am I even close to the correct dilution and please don't tell me in equations because I can't understand them. What I do understand is what I've described, one teaspoon MB and 9 teaspoons of water.
2. I need to have specific information on how to give the MB to my mother and in which combination, taurine/potassium (which I don't think that she can have because of her high blood pressure)/baking soda? etc. As soon as possible please?
She weighs approximately 140 lbs, she's 5ft 2 inches tall. She's on medications, metoprolol and aspirin. I have spoken with a pharmacist who has said that there are no contraindications with her meds and the MB.
Please, she's feeling the effects and I know she's very frightened, the docs seem to think that the PD was set off by a mild stroke that she had just after my dad died almost 3 years ago. He died of institutionalized pnuemonia/parkinsons. She is not taking any parkinson's medication at this time.
I know that you all get a lot of emails asking for advice so I am not asking to be "special" I am just asking for clear concise and reliable answers as soon as you are able to. Thank you for your time and experience. I look forward to hearing from you soon.
I got some methylene BLUE (we're talking blue) from a pet store--the only place I could find it. It says not for medicinal, human or animal use--but I took a couple drops anyway because they always say that stuff. Is there a different kind I should have gotten? Ted said it was the stuff for fish tanks so that's what I got. I thought I should maybe check before I took any more. If someone could email me directly I would appreciate it. I don't think it would take much of the stuff before you could give the Blue Men a run for their money--or at least a Smurf. If it matters, I forgot to mention I got it for Parkinson's.
(Fort Worth, Texas)
(Pleasanton, Ca 94566 U S A)
(San Fernando, La Union, Philippines)
Methylene Blue and Vitamin C
Methylene blue can be purchased in two forms: pre-mixed with other elements or in a 'pure' state. ... What form is referred to by 1.0% and 9.1%? ... When adding 100 cc of methylene blue to 900 cc of water, what form of methylene blue is used - the pre-mixed or the 'pure'? ... How much Vit C is taken together with methylene blue? ... I'm asking because I would like to try methylene blue and vitamin C for my Parkinson's. ... I am 78 years old, diagnosed as having Parkinson's in 1998.
(Charlotte North Carolina)
Methylene Blue and Vitamin C
I am amazed that after one and a half days of taking methylene blue with vitamin c my 85 year old dad, who has Parkinson's, initiated transfer to his wheelchair and needed much less assistance than yesterday. Yesterday he was not weight bearing much. This morning I did not pick him up to get in his chair, just guided him. I broke out into laughter of happiness!
Thank you a million for the information you provide on earthclinic. I love seeing the results!
(Belfast, Northern Ireland)
(Fort Worth, Texas)
(South Bend, IN)
(RSM, CA, USA)
(Fort Worth, Texas)
(Fort Worth, Texas)
(Fort Worth, Texas)
(Mumbai , Maharashtra/India)
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(Manganui, Northland, New Zealand)