Parkinson's Disease Tulip


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Old 09-20-2014, 01:04 AM #31
Glen Pettibone Glen Pettibone is offline
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Default Intranasal Glutathione

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Originally Posted by villiers View Post
hey GLEN

I have bought your book,
really mind blowing !!!!
but please,where do you get your intranasal glutathione ?
which brand are you using ?

kind regards
Hi Villers,

Dr Mischley prescribed the Intranasal Glutathione for me from Key Compounding pharmacy in Seattle.

Try to find yourself a naturopathic doctor to help.

Glen
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Old 09-20-2014, 08:57 PM #32
Horsegoer Horsegoer is offline
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Default

The only way to buy the book is on kindle...

I want to send it to my dad
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Old 09-20-2014, 09:09 PM #33
Glen Pettibone Glen Pettibone is offline
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Default There is a free Kindle reader

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Originally Posted by lurkingforacure View Post
Hi Glen, do you have a non-kindle version of your book available?
Hi Lurking,

FYI there is a free Kindle reader for PC or Mac. Google "free kindle reader"

Cheers

Glen
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Old 09-20-2014, 09:39 PM #34
lurkingforacure lurkingforacure is offline
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Default do you know the %?

Quote:
Originally Posted by Glen Pettibone View Post
Hi Villers,

Dr Mischley prescribed the Intranasal Glutathione for me from Key Compounding pharmacy in Seattle.

Try to find yourself a naturopathic doctor to help.

Glen
Glen, I've found a couple of places online that claim to sell this, one even says it is 10% intranasal glutathione...do you know what concentration yours is, and how much you take? Do you whiff some several times a day, or whenever you feel like you need it, and how do you know how much you are getting?

Thanks, since my reading indicates it has very few side effects, I'd be willing to get some online if I had a better idea of how closely it resembled what a compounding pharmacy would make.
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Old 09-21-2014, 07:00 AM #35
soccertese soccertese is offline
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Quote:
Originally Posted by lurkingforacure View Post
Glen, I've found a couple of places online that claim to sell this, one even says it is 10% intranasal glutathione...do you know what concentration yours is, and how much you take? Do you whiff some several times a day, or whenever you feel like you need it, and how do you know how much you are getting?

Thanks, since my reading indicates it has very few side effects, I'd be willing to get some online if I had a better idea of how closely it resembled what a compounding pharmacy would make.
lurking, i'm in seattle and have attended two pd support group meetings where Mischley spoke. she made the point that glutathione breaks down very rapidly and she had gt from different sources tested and only key pharmacy knew how to preserve it. don't know if true or not.. btw she isn't a MD but a naturpath. she hasn't published yet her 1st nasal gt study funded by the NIH as far as i know which only tested safety, not efficacy. i have spoken to at least 3 pd''ers that got gt rx's from Mischley for gt and saw no benefit. at one of the support meetings i believe she said she considers it more neuroprotective than for reducing pd symptoms. of course everyone is different, might help some not others. keep in mind that dr's hauser AND PERLMUTTER published a paper showing no benefit from IV gt in pder's in a small double blinded trial.

Mischley said she was getting calls from neuros about nasal gt so i imagine your neuro could write an RX for you. my advice is get it from key pharmacy to make sure your're getting "good" liquid gt assuming you can afford it, i've heard it's $75/month delivered refrigerated, might be wrong. here's their website
http://www.keycompounding.com/


i have no connection to key. i'm not encouraging anyone do this but just want to put in my 2 cents. i haven't tried it but might. tried IV GLUTATHIONE back in 2003 and noticed no affect but symptoms were very mild. got rx from my neuro, he's open to trying alt-meds, and got supplies from local compounding pharmacy, nurse friend gave me the IV'S.

kind of surprised there's not many pd'ers posting on the web about it if it really made a difference. that would be the first thing i'd do.

Last edited by soccertese; 09-21-2014 at 09:34 AM. Reason: changed oral to nasal
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Old 09-21-2014, 11:24 AM #36
lurkingforacure lurkingforacure is offline
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Default Many thanks:)

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Originally Posted by soccertese View Post
lurking, i'm in seattle and have attended two pd support group meetings where Mischley spoke. she made the point that glutathione breaks down very rapidly and she had gt from different sources tested and only key pharmacy knew how to preserve it. don't know if true or not.. btw she isn't a MD but a naturpath. she hasn't published yet her 1st nasal gt study funded by the NIH as far as i know which only tested safety, not efficacy. i have spoken to at least 3 pd''ers that got gt rx's from Mischley for gt and saw no benefit. at one of the support meetings i believe she said she considers it more neuroprotective than for reducing pd symptoms. of course everyone is different, might help some not others. keep in mind that dr's hauser AND PERLMUTTER published a paper showing no benefit from IV gt in pder's in a small double blinded trial.

Mischley said she was getting calls from neuros about nasal gt so i imagine your neuro could write an RX for you. my advice is get it from key pharmacy to make sure your're getting "good" liquid gt assuming you can afford it, i've heard it's $75/month delivered refrigerated, might be wrong. here's their website
http://www.keycompounding.com/


i have no connection to key. i'm not encouraging anyone do this but just want to put in my 2 cents. i haven't tried it but might. tried IV GLUTATHIONE back in 2003 and noticed no affect but symptoms were very mild. got rx from my neuro, he's open to trying alt-meds, and got supplies from local compounding pharmacy, nurse friend gave me the IV'S.

kind of surprised there's not many pd'ers posting on the web about it if it really made a difference. that would be the first thing i'd do.
Thanks so much, ST. I did read about Perlmutter's study (was really hoping that would have a different result, though). Seems like I've read more about people with ALS trying this intranasal gt than I have PWP. I guess it's worth a try, heaven knows we've tried so many other things, what's one more!
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Old 09-21-2014, 11:06 PM #37
Glen Pettibone Glen Pettibone is offline
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Default Links to Blog, Book - One Time Only

Hello All,

I've been given permission to post links one time.

I've written a book with full details of my story and my diet.

It is entitled "Powerful Food & A Walk In The Sun (Parkinson​'s Relief Was In The Supermarke​t)".

I thought you might be interested. Here is the info:

It is available on Amazon at the link:

http://www.amazon.com/dp/B00MEBATMW#_

or from the UK and Ireland at:

http://www.amazon.co.uk/gp/product/B...=1&*entries*=0

You can download a free Kindle reader for your computer (there may be an app for your Apple product also) at:

http://www.amazon.com/gp/feature.htm...l_9ns220msf3_b

I've also started a blog at:

http://powerfulfoodandawalkinthesun.blogspot.com/

At my blog, I've posted links to redio blog interviews I've done with Dr. Robert Rodgers of http://www.parkinsonsrecovery.com/.

I have been hosting Sunday Connections about every seven weeks.

There are two, one hour shows posted that anyone can listen to for free to hear my story.

I hope this helps all the suffering.

God Bless,

Glen Pettibone

*admin edit*

Last edited by Chemar; 09-22-2014 at 06:16 AM. Reason: NeuroTalk Guidelines
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Old 09-21-2014, 11:13 PM #38
Glen Pettibone Glen Pettibone is offline
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Default Intranasal Glutathione (ING)

Quote:
Originally Posted by lurkingforacure View Post
Thanks so much, ST. I did read about Perlmutter's study (was really hoping that would have a different result, though). Seems like I've read more about people with ALS trying this intranasal gt than I have PWP. I guess it's worth a try, heaven knows we've tried so many other things, what's one more!
Hi Lurking,

Several comments:

-ING has helped me with arm-swing and rigidity.
-ING is known to coordinate recycling of antioxidants.
-ING also powers microphages that chelate and cleanse toxics.
-Mischley has now published in think two papers on ING (one for sure).
-Google YouTube videos "gluthione perlmutter".
-I'm going to try switching to a local compounding pharmacy to save shipping cost, I'll let you all know how that goes.

Glen
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Old 09-22-2014, 09:42 AM #39
Glen Pettibone Glen Pettibone is offline
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Default Concentration

Quote:
Originally Posted by Glen Pettibone View Post
Hi Lurking,

Several comments:

-ING has helped me with arm-swing and rigidity.
-ING is known to coordinate recycling of antioxidants.
-ING also powers microphages that chelate and cleanse toxics.
-Mischley has now published in think two papers on ING (one for sure).
-Google YouTube videos "gluthione perlmutter".
-I'm going to try switching to a local compounding pharmacy to save shipping cost, I'll let you all know how that goes.

Glen
Also I'll find the concentration and post it.

Glen
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Old 09-24-2014, 11:47 PM #40
Glen Pettibone Glen Pettibone is offline
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Default Concentration of ING

Quote:
Originally Posted by Glen Pettibone View Post
Also I'll find the concentration and post it.

Glen
The concentration of my ING is 200 mg/ml, two sprays each nostril twice each day.

God Bless

Glen Pettibone
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