Glutithione Spray: I was curious about... - Cure Parkinson's

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Glutithione Spray

Bythejerseyborder profile image

I was curious about glutithione Spray. I bought some from ageless Rx. I thought intravenous would be too expensive. I will post after a month if I see a difference. My primary doctor keeps mentioning to look into glutithione. Right now I do Mucona capsules boxing and walking.

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Bythejerseyborder profile image
Bythejerseyborder
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34 Replies
FawnLily profile image
FawnLily

Is it the nasal spray? I am curious how it works for you. Are you going to have blood levels checked before and after? I am taking 10 pumps liposomal glutathione orally daily. Seems like the spray would be easier. The liposomal glutathione is messy and doesn’t taste great. And it’s pricey at 3 bottles per month for the 10 pumps daily.

Bythejerseyborder profile image
Bythejerseyborder in reply toFawnLily

I just had blood work done. This particular brand was $110. I can get it for $100 delivered automatically monthly. They say that a nasal spray gets through the blood brain barrier. It doesn't taste like anything. Does your oral version work for you?

FawnLily profile image
FawnLily in reply toBythejerseyborder

I’ve been taking it for a month. The only change so far was a firming up of my poop. But my symptoms were already well managed with c/l, B1, and mannitol. I am early stage. I just dropped my c/l dose 2 weeks ago so waiting to stabilize from that.

gregorio profile image
gregorio

I am very interested in following this thread. I have had a look on line but can not find nasal spray, just the oral version. I live in Europe but normally find everything on Amazon

Bythejerseyborder profile image
Bythejerseyborder in reply togregorio

I'm using Ageless Rx brand. I didn't find that brand on Amazon.

Chris1960-2 profile image
Chris1960-2

You can use NAC (N-Acetylcysteine) too (1200mg-1800mg/day) as a glutathione precursor.

goldengrove profile image
goldengrove in reply toChris1960-2

Do you use NAC and do you need to take it with glycine? I bought some of both for my hwP but then chickened out of pressing him to take it. Does anyone use NAC? I began using the glycine and it seems to have helped me stay asleep the whole night.

Astra7 profile image
Astra7 in reply togoldengrove

I’ve taken NAC for 5 years since diagnoses. Still going ok (havnt told people at work etc ), though recent problems with freezing/falling while playing tennis.No way of knowing if the NAC has been a factor.

MarionP profile image
MarionP in reply toChris1960-2

Had not realized that back is glutathione precursor, will look into the mechanisms, watching and learning about this intersection with NAC, sometimes I'll pull and sometimes rather controversial, should be very interesting.

Chris1960-2 profile image
Chris1960-2 in reply toChris1960-2

Look at this trial : santelog.com/actualites/par...

134A profile image
134A in reply toChris1960-2

Is there an English version?

Chris1960-2 profile image
Chris1960-2 in reply to134A

www-santelog-com.translate.... (Google translation)

134A profile image
134A in reply toChris1960-2

Thanks Chris

134A profile image
134A in reply to134A

I was given NAC a few years ago by a naturopathic doctor but it got lost in the pile of supplements that ended up on my kitchen counter! I believe there’s still some in the back of a cupboard. Perhaps I should give it another go.

Chris1960-2 profile image
Chris1960-2

I give NAC to my mum who is a PwP. Didn't know it could/must be taken with Glycine.

MarionP profile image
MarionP in reply toChris1960-2

Hold on, must it? More on that please

Chris1960-2 profile image
Chris1960-2 in reply toMarionP

Look at the trial above mentioned.

LAJ12345 profile image
LAJ12345 in reply toChris1960-2

? I can’t see the mention of glycine?

Chris1960-2 profile image
Chris1960-2 in reply toLAJ12345

No mention of Glycine. Only NAC in this trial.

Bolt_Upright profile image
Bolt_Upright in reply toChris1960-2

I got scared off of Glycine. Of course, I could be way wrong. healthunlocked.com/cure-par...

SuuSuu profile image
SuuSuu

I was in Laurie Mischley's 2015 study on intranasal glutathione. I had taken NAC since my diagnosis in 2013, and had to do a 90 day washout prior to the study. I noticed a more rapid progression of symptoms during that time. (NAC is a precursor to glutathione) When I "snorted" my first dose of intranasal glutathione I had an immediate response...I could process visual stimuli faster, had smoother gait and better hand dexterity etc. The glutathione was not very stable, had to be kept in the frig and was specially formulated at a compounding pharmacy.

You can google the study, her results were inconclusive but I know it had a profound affect on me. We did a 30 day washout after the 90 days of glutathione. At $300-400/month for glutathione I opted to return to the NAC. When I later did one month of the intranasal glutathione (while doing NAC) I noticed very little impact. My analysis - Glutathione had a significant impact alone, but the NAC provided similar results (for about $10/month).

Dr. Mischley insists that NAC is an excito-toxin with ill effects to the brain and poor outcomes. She recommends oral glutathione. We all know that doesn't cross the blood brain barrier, yet results of her Modifiable Variables in Parkinsonism (MVP) Study indicates glutathione supplementation improves PD. She suspects taking it orally supports other glutathione hungry organs (the liver and lungs) allowing for an increase of glutathione to be generated in the brain.

(I don't know anything about glycine and NAC...)

goldengrove profile image
goldengrove in reply toSuuSuu

So, SuuSuu, you still use NAC regardless of Dr Mischley's disapproval? Can I ask if you have tremor and whether the NAC seems to have helped with that? Also do you use 600mg twice a day?

SuuSuu profile image
SuuSuu in reply togoldengrove

I do use it at 600mg. once a day, sometimes twice/day. I do alternate with glutathione 500mg every month or so -- a bottle of one and then the other. I can't tell a difference between the impact on symptoms. They both help. I have great respect for Dr. Mischley, but I make my own choices... I should ask her for her research sources on NAC -- I might re-think it then. ...And no, I don't have a tremor.

SuuSuu profile image
SuuSuu

Dr. Mischley is still recruiting for her Modifiable Variables in Parkinsonism (MVP) Study. It amounts to reporting about meds, symptoms, supplements, lifestyle, diet etc. online every six months. You can learn more here: mvp-study.com/ -- I've participated for six years. It's a way to move research forward!

Raphaekg profile image
Raphaekg

The research shows that the intranasal route does indeed increase brain levels of glutathione. Unfortunately, research showed that it didn't improve symptoms more than a placebo saline spray. So, it's probably an expensive waste. ncbi.nlm.nih.gov/pmc/articl...

BlueHawaii profile image
BlueHawaii

I don't know anything glutathione. What is it? And what does it do for pwp?

ElliotGreen profile image
ElliotGreen

I make my own glutathione nasal spray. I order glutathione powder in the UK from blackburndistributions.com. I dissolve it in distilled water and use a cheap nasal pump that I bought off of Amazon. I keep it in the refrigerator and make a new bottle every week or so.

I take it before I go to bed. For the first two or three weeks that I took it, I noticed a DRAMATIC improvement in my sleep. Suddenly I was sleeping eight hours straight through. It was amazing. (My sleep stack also includes cannabis oil and melatonin.)

I continue to take glutathione, but sadly the sleep benefit has not lasted. It's hard to know whether the underlying Parkinson's has gotten worse, or something else has happened.

Despe profile image
Despe in reply toElliotGreen

Have you tried Magnesium Glycinate in combination with Melatonin? It has been very effective for my husband who used to get 5-6 times at night to go to the bathroom. He now sleeps through the night, getting up about 6:00 a.m. for his first bathroom trip. :)

simonasays profile image
simonasays in reply toDespe

What dosage of Mag and Melatonin does he take?

Despe profile image
Despe in reply tosimonasays

Magnesium Glycinate by Klaire Labs 2 caps (300mg). Melatonin 3mg fast dissolving.

ElliotGreen profile image
ElliotGreen in reply toDespe

Thanks. It's worth a try.

I take magnesium citrate. Is there a benefit to taking magnesium glycinate instead?

When does he take the magnesium?

Despe profile image
Despe in reply toElliotGreen

Mag Glycinate is for sleep. There are different types of Magnesium: Threonate (brain health) , Taurate (Cardiovascular Support) , Glycinate (Mood and Sleep Support) , Malate (Energy Support), Orotate (Athletic Performance and Recovery), Aspartate (Muscle Function and Neurotransmitter Support), Oxide (Regularity), and Citrate (General Well-Being).

There are Magnesium supplements that combine different types of Magnesium.

ElliotGreen profile image
ElliotGreen in reply toDespe

Wow. Thank you.

Despe profile image
Despe in reply toElliotGreen

You are welcome. My husband takes Magnesium Threonate during the day (3 caps) and Glycinate (2 caps) an hour before bed. The addition of Melatonin worked wonders for a good night's sleep. He has had nocturia, but since he started this combination, he sleeps through the night without the frequent bathroom trips.

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