Elbert,
If I were you, I would consider making a liposomal formula of gluthathione.
You can make it very similar to how Vitamin C is liposomized. In fact, if I
were you, I would combine both Vit C and gluthathione in a protocol. This
should save you huge dollars if it seems effective for your dad.
doug
----- Original Message -----
From: Elbert vaughn
To: [email protected]
Sent: Friday, December 07, 2012 11:29 AM
Subject: CS>Gluthathione for Dad/need advice/Parkinsons disease
Dear Silver list family, I would greatly appreciate any advice that could
help me make the right descision in regards to the treating of my dad with
Glutathione therapy. I have become aware that this antioxidant(we all produce
it, but it diminishes as we get older), gives unbelievable results when given
to Parkinsons patients(you can go to youtube, and put parkinsons patients being
treated with glutathione, and see what I mean). Their are parkinsons patients
when taking intravenous glutathione that are walking without assistence(a hour
after taking glutathione), speaking cohenrently(a hour or more after taking
gluthathione). It works that fast. I could not believe what I was seeing. The
only problem is that it cost a fortune(many hundreds or even a thousand dollar
per month or more(has to be given by a trained proffesional in a clinical
setting, because I heard that you could do harm(possibly kill someone if you do
not know how to give intravenous injections, which I don't know how to do). I
don't believe you can get a prescription for glutahione, because it is not a
drug, even though on the internet it says you can get a prescription for
Glutathione(generally used for treating arthrithis, and asthma). We will have a
appointment with my Dads neurologist to see if it is possible to get a
precription(and hopefully if he gives us a prescription for Glutathione his
insuranace company will cover it). I hope, and pray that will be the case.
Their are 3 ways of administering glutathione(supposotories,
inhaled(nebulization), and intravenous). We have tried the supposotories, and
at the current time my Dad is on nebulization). The supposotories were much
more effective(I guess the key to the success rate of glutathione is getting it
directly into the blood. The nebulization not so effective in my eyes, but we
can only afford the nebulization. The supposotories cost $179 per month. The
nebulization cost $35.00 a month(which we can afford, if I can get my mother to
believe that it is worthwhile( it says on the internet that glutathione can
slow, or even halt the progression of parkinsons disease). My mother is
looking for results the parkinsons patients on youtube got from glutathione
being administered intravenously, I don't think that is possible with inhaled
glutathione.
So, my mindset at the time is how can I become educated on how to give my dad
intranvenous glutathione. I will be contacting a nursing agencies, and pay for
a nurse to show me how to give a person intranvenous injections. I can purchase
the equipment needed(syringe, tubing etc) that is needed to give intranvenous
injections. Liquid glutathione can be purchased off of the internet(even though
the prices are something we cannot afford). I have done research, and found
that a product call immunocal, and lifewave patches can cause the body to
produce more of it on natural glutathione, and according to the internet(I am
speaking more about the lifewave patches) can simulate what I saw on youtube
with the intravenous glutathione(again prices very high for immunocal, and the
lifewafe patches). Their was a person with parkinsons disease that put on the
lifewave patches on youtube, and basically had the same results as a person
taking intravenous glutathione would have. The results were immediate(even
though I am skeptical about lifewave patchs(my mothers friend had some aliment
that the lifewave patches were suppose to allieviate, but got no results). So
basically what I am trying to do is to find something that we as a family can
afford that can give the same or similar results that a parkinsons patient
recieves when taking intravenous glutathione, that is, if I cannot find
affordable liquid glutathione from off the internet(injectable glutathione) ,
because if I am not able to find affordable liquid glutathione we as a family
wlll not be able to treat my father with intravenous glutathione. God knows I
will be forever grateful if anyone has any suggestions to help me achieve this
goal. Here are a couple of weblinks(from youtube), that indicates what happens
when a parkinsons patient takes intravenous glutathione. Here they are: 1)
http://www.youtube.com/watch?v=uQRCpdcGwIU
2)http://www.youtube.com/watch?v=uEsl1aOyLHE and 3)
http://www.youtube.com/watch?v=k9sVN7OIKMg&feature=BFa&list=UUSWnNWGvnVTLD9y3oYgMXmg
If you have any advice that can help us as a family achieve results similar
to what those websites show, or that can help us achieve the maximum results as
possible with glutathione therapy, as it pertains to the treating of
Parikinsons disease, any advice on how we as a family can treat my father in a
affordable way with intravenous gluatathione we as a family of course it goes
without saying would be eternallly grateful for your advice.
Also, I want to take the time to thank the silverlist family for giving me
adivce(I have diabetes, and my diabetes is responsible for my cataracts(I am
the guy that posted a request, asking for advice for my cataracts(I am the guy
with no health insurance). So I just want to thank the memembers who took the
time to reply to my request, and give me suggestions. Okay, that's it. God
bless you all, and may you all have a merry christmas. Elbert Vaughn
