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TOPIC: MMS and Parkinsons Disease

MMS and Parkinsons Disease 19 Sep 2017 07:52 #56428

Can anyone tell me if taking any of the MMS Protocols would benefit a patient with Parkinsons Disease. If so - can it be taken along side regular allopathic medication? As Parkinsons Disease is due to a lack of Dopamine - can the MMS correct this condition? Or could just getting rid of the heavy metals and pathagons help this condition. A family member has just been diagnosed with this illness and I want to do anything I can to help. Thank you.
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MMS and Parkinsons Disease 19 Sep 2017 08:45 #56429

From Jim Humble's newest book, MMS Health Recovery Guidebook

Diseases Generally Considered Incurable

There are many diseases generally considered to be incurable. We have nevertheless received countless reports from people worldwide who through using MMS have been recovered to full health from many of these supposedly incurable diseases. Some of these include ALS (Lou Gehrig's Disease), Alzheimer’s, autism, cancer (all kinds), leukemia, multiple sclerosis, Parkinson’s, polio, rheumatoid arthritis, and many other life threatening diseases.


Follow the Health Recovery Plan (HRP) as outlined in the book. The book also discusses taking meds with MMS.
2 ml of 3000 ppm original CDS equals a 1 drop MMS1 dose in a normal stomach
www.mmsinfo.org/infosheets/mms1_equates_to_cdh_and_cds.pdf
Telegram Channel: t.me/MMSinfo
Websites: MMSinfo.org * www.facebook.com/groups/ebolacures/
Instructional Videos: www.youtube.com/channel/UCXv6hCnvjMmGg4_AYq4wlNw
Instructional Videos: www.brighteon.com/channel/clo2works
Answers to many questions are in Jim Humble's books: jhbooks.org/
How to use CDS, CDH in Protocols: www.mmsinfo.org/infosheets/CDS_CDH_and_Protocols-2.pdf
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MMS and Parkinsons Disease 20 Sep 2017 05:41 #56437

Thank you for this information. I shall try to order Jim's book online.

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MMS and Parkinsons Disease 20 Sep 2017 08:04 #56439

At the present time this is the only place selling Jim's newest book.
2 ml of 3000 ppm original CDS equals a 1 drop MMS1 dose in a normal stomach
www.mmsinfo.org/infosheets/mms1_equates_to_cdh_and_cds.pdf
Telegram Channel: t.me/MMSinfo
Websites: MMSinfo.org * www.facebook.com/groups/ebolacures/
Instructional Videos: www.youtube.com/channel/UCXv6hCnvjMmGg4_AYq4wlNw
Instructional Videos: www.brighteon.com/channel/clo2works
Answers to many questions are in Jim Humble's books: jhbooks.org/
How to use CDS, CDH in Protocols: www.mmsinfo.org/infosheets/CDS_CDH_and_Protocols-2.pdf

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MMS and Parkinsons Disease 20 Nov 2019 11:28 #61702

To save time, I will paste my post from healthunlocked.com...I My father has been diagnosed with Parkinson's in september 2017. He is 75 years old and took Madopar (Levodopa/carbidopa) for 6 month. Before the diagnose we saw that he might have Parkinson because he walked slowly with small steps(around10cm and close to the ground( around 10cm) -in contrast with his high speed walking before. He was almost always stressed for one reason or another(he had years before panic attacks, could not sleep, woke up in the middle of the night and said He is paniced )and after the hot summer time(he mostly stayed at home) we noticed the slow walk and strange, fearfull look on his face . Before he got to the doctor, we gave him ginco biloba, tonotil, b complex for 2 weeks and his walk improved to almost normal and his mood too. After he started the madopar for 2 weeks he was looking unusually happy, after that he started to feel sleepy, and dizzy and he was saying that he felt the best before he went to the neurologist. We started to search online for alternative treatments and we searched for MMS (which is a test for the skills of the Parkinson's patients) and found out this way about MMS a.k.a .Master Mineral Solution discovered by Jim Humble (more info atmmstestimonials.co ) which is used for curing cancer, diabetes,Alzheimer's, autism, Parkinson's and other diseases. After 6 month on Madopar we decided to try mms after 1 week of reducing the dose. Later we found out that the safe period of getting off the official medication is 10 weeks-in the book by Dr. Janice Walton-Hadlock, medications_complete.pdf you can download for free pdrecovery.org/publications/ along with other books if you want to understand the causes and alternative treatments- she cured more than 300 patients without falling back if they did not take dopamine enhancing medication for more than 3 weeks. Generaly she could cure patients who took medication for longer , but if they got stressed they would get the Parkinson's again...so she is against starting the classic medication.My father's diagnosis according to Dr. Janice Walton is self-induced pause which is caused by physical and /or physical stress and the treatment must start by prayer...and then improved by Yin-Tui-Na.

We reduced the dose to 0 in 1 week, gradualy replacing Madopar with 2 drops of MMS in 200ml water.

After the first dose of MMS (2+2) his speech was much better and his walking was the same. He started to take l-tyrosine 500mg in the mor and 5htp 200mg in the morning. Between the meals he took 1 to 3 times per day MMS amd he was feeling better walking a little bit better. He walked daily with my mother. After 4 month the hot summer started, he didn't went out and he begun to freeze , we got scared,did not get why...we reduced the tyrosine and the 5htp and remained only on the MMS ang he got better. The MMS has a quick and powerfull positive effect on him without any side effect but the effect last only 1-1,5 hours. He also takes B vitamins, coconut oil, curcumin,hemp oil for omega 3,6,9, magnesium. The problem with the MMS is that it should be taken 8 times each day, but he would take it only 1-5 times. His old headaches went away, also his constipation. When he had only 1 or 2 doses, he'walking and mood was worse he didn't recognize my mom ,my brother, or me, and when he had it 4-5 times, he was better. One day he fell and broke his upper leg(small crack). We took him to the hospital, x-rayed him for like 5 hours and in the meantime he had to go to the bathroom...but the hospital's stuff were moving so slowly...and he urinated on himself...after that day he started to go to the toilet 5-10 times every night. After 3 weeks his leg healed and we went for 1 hour walks but his walking was with fear of falling... One month ago he fell again and got a nasty scratch on his bottom. After this falling he is walking in lower position, with smaller steps and his weight is put on his toes and only with his walker.

Looking back it seems that every stress, trauma is getting him in to panic mode with worse simptoms, but has moments when he walks quite ok, so the dopamine producing cells not working theory may not be true...it seems that the dopamine is blocked by the panic according to Dr. Janice Walton.

I have also noticed that he is better in every way 20-30 minutes after taking the MMS (2+2drops)with or without DMSO(4 drops). Before every walk we would drink MMS and 1-1,5 hours after that he was quite ok, it seems magical. After the 2 falls he is now at his lowest and it changed rapidly, which should be because of the stress.

If stress causes something it should be improved if we reduce the stress, and so far MMS is the best and quickest to improve his state(in the daytime sleeps much better after the dose), even if he did not believe in it so far(now with Dmso for quicker and better effect, and mms and dmso can enter the brain).

One lady with age over 80with Parkinson's who took madopar for 3 years could not get out of her bed(was also badly shaking) , reduced medication to 0 in 1 week and after 1 more week she got out of her bed and walked in the garden alone after taking mms 2+2 drops gradualy instead of her Madopar. After that took Mms 6+6 drops 4 times.

We watched the documentary Heal on Youtube, I highly recommend it- abot the power of positive thinking.

His sleeping is worse, he sleeps during daytime too, at night is waking up 5-10 times - often with bad dreams which seem real to him - after he broke his leg, so far he would not take sleeping pills, once tried melatonine without good effects. Now we try L-theanine and hope for the best.

The B1 should arrive, not sure how to find the right dose, will start with 100mg per day.
After 2 month we tried 2ml injectable b1 once per week so far for 6 times. To make the long story short, so far mms(3 drop duse -we use mineral water 120ml and apple juice and cola) with or without dmso is helping him move better 30 minutes after he takes it, but he takes it only 1-4 times per day. His mood and movement is closely related to the frecvency of the doses. If he takes just 1 dose in the morning, in the evening he can't stand up and barely walks. If he takes 3 or 4 doses he moves much better. We tried b1, b12, complex B, arginine, ornithine, ....now melatonin and l-theanine for sleep, which is helpfull, but nothing had as good and as quick effect as the MMS drops with hcl activator, plus it is hard to find the right dose for the vitamins and supplements...
With the mms is easyer, because you see the effect in 30 minutes...and you slowly increase the frecvency and after reaching 8 times per day after some time you can increase the drops. We will try vitamin D(coimbra protocol) high doses and b12 high doses.
All the best wishes!
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MMS and Parkinsons Disease 21 Nov 2019 04:32 #61706

Ketogenic diet likely is key for helping and preventing neuro-degenerartive diseases.
Important clue is the brain is made of mostly fat.
While MMS may help and alleviate, I don't believe it can cure Parkinsons.

I almost had a friend travel to a clinic last winter. But he got in too bad of a shape to be motivated to do something about his Parkinsons. Too late. He passed away 2 months ago.

Nevertheless here's a promising testimonial from the above mentioned clinic:
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MMS and Parkinsons Disease 21 Nov 2019 14:43 #61709

mart1n wrote: Important clue is the brain is made of mostly fat.

That is, the kind of fat the "authorities" have been warning us against for 3 generations now, and which appears to have been deadly disinformation all these years.
Another important clue is that Alzheimer/dementia seems related to Parkinsons. And Alzheimer is currently being rebranded to diabetes 3, in short meaning the brain has stopped using sugar/glucose for energy. Without healthy fats the Alzheimer brain, and probably the Parkinsons brain as well, will shrink and degenerate.

One more clue concerning neuro-degenerative diseases is the proven connection between cholesterol lowering medication -$tatins-, often in conjunction with low fat wrong fat diet, and ALS. Neurons depend on cholesterol for transmitting signals. Little cholesterol, bad transmission..

While MMS and other oxidants may be of help and perhaps should be part of treatment, you will need to provide the brain with the correct fuel in order for it to stay in shape.

Those not having the money to travel to clinics like NeoMed in Cyprus: Most of what they offer can be done at home and is rather cheap. For example the ozone therapy they use can be replaced by MMS. Dietary changes can be implemented at home today. Quit the statins and use garlic instead. Garlic actually helps cardiovascular health. Statins make things worse. Proven that as well.
Stay away from the recommended "vegetable" oils and margarine, and basically all processed foods that contain these. Healthy, regenerating fats are coconut, olive, real butter, ghee, lard etc. These fats are compatible with the fat in our brains.
Quit sugar and grains.

May this be of help getting on track of prevention and working treatments.
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Last edit: by mart1n.

MMS and Parkinsons Disease 21 Nov 2019 15:14 #61710

Dear My,
From what you're saying it sounds like MMS is really helping so if I were you I would follow my suggestions in the following forum post to get it into him with every drink of water he takes all day long 24/7/365 days a year. I did this for 3 years as a personal experiment and for my personal health maintenance. It's the easiest way to take MMS. If you do it you may want to start with 2 drops per liter and then gradually work up to 4 to 5 drops per liter of water. It does alter the taste of the water a bit but in time you get used to it and don't even notice it. By the way almost all autopsies done on alzheimers patients show herpes viruses in the brain and it's my belief that CLO2 over time (like years) can probably get into the brain and clean it up. I think Parkinsons is similar.

mmsforum.io/goto/mms-mms1-research/30839-non-acidified-sodium-chlorite-for-disease-prevention-and-healing?start=0

Hope it helps,
Scott
- I'm Scott McRae, the creator of CDH with the help of CLO2 (Charlotte Lackney)

- I did a CDH injection / Chlorine Dioxide (CLO2) injection / IV push of 10ml of dilute 50ppm CDH / CLO2 into my blood 3 times in 11 hours & did before & after blood tests that showed that it did NO HARM to my blood, liver or kidneys. This suggests the possibility that CDH / CLO2 is a potential LIFESAVING MRSA cure, VRE cure, CRE cure, AMR cure, Ebola cure, HIV cure, Cancer cure, etc., since it appears to be safe intravenously at 50ppm.

- I started the Facebook group "The Ebola Cures" to inform the world that CLO2 & other oxidizers can cure Ebola
- Every ml of CDH contains 1 drop of MMS, so 1 drop of MMS = 1ml of CDH
- MMS is 7 to 10% activated in 30 seconds while CDH made with 4% HCl is about 50% activated in the bottle. This is why CDH is far less nauseating than MMS drops
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Last edit: by Truthquester.

MMS and Parkinsons Disease 21 Nov 2019 20:09 #61711

Scott, the herpes/Alzheimer connection is new for me. But I did know Parkinsons patients often have inflamed areas in their brain.

If a herpes virus is responsible for Alzheimer then the primary cause would be low immune function and which allows the virus to establish itself. Toxins generated by a virus infection would cause inflammation and degeneration of brain tissue.
One would have to get rid of the virus and restore immune function. But regenerating brain tissue and function doesn't necessarily happen all by itself as soon the virus is gone. Especially older people would need to focus on specific nutrition for repair (and also restore intestinal flora, which detoxing alone won't do either).

Regardless of cause, all degeneration will reduce/impair brain function. Whatever it is that causes the inflamation MMS will almost certainly make a difference for the better. But for many, if not most, detoxing and/or getting rid of virus is only a first step.

Unfortunately my friend never would take MMS. He always turned away his head when I talked about what it can do. He was unable to wrap his mind around the tiniest possibility of me having better meds than his doctor..
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