Re: Parkinsons/off topic

[Guest guest]

Hi CJ,

----The "push" drug, also known as glutathione? It's the body's major antioxidant (and at low levels in PD patients) and glutathione push therapy for Parkinson's has been pioneered by Dr. Perlmutter, a neurologist in FL. -

Thanks

Aletha

Original Message -----

From: kathy lintzenich

low dose naltrexone

Sent: Sunday, May 29, 2005 4:28 PM

Subject: Re: [low dose naltrexone] Liquid LDN

aletha, what kind of treatment is it for parkinsons?

Re: [low dose naltrexone] Liquid LDN

In a message dated 5/29/2005 3:02:40 AM Central Daylight Time, Aletha@... writes:

That is great CJ. I just didn't know enough about it in order to advise for it. Do you have to refrigerate it? Does the pharmacy turn it into a liquid solution, or do you?

Kind regards

Aletha

Yes, Aletha is has to be refrigerated. I mix a 50 mg pill with 50 ml of distilled water. ( I crush the 50mg pill and mix it myself with the water.) It works just great and I much prefer doing it this way and then I do not have to worry about fillers.

I have to say that I truly believe that the Lord lead me to the LDN website. I had just found out that I had three new huge lesions and what scared me the most was the big one on the brain stem. I knew that if I did not get something I was going to be a goner. I have had MS since I was 13 years old but I did not have my first major attack until July 11, 1988. After that I went slowly downhill. When I started the LDN I had nothing to lose and everything to gain. I researched it enough to know that I JUST HAD to get it and my neuro would not write me a script for it. So I had to take my health into my own hands. I will NEVER regret getting started on it. I was pretty much apt. bound and I had this huge fear of going into a nursing home. The LDN stopped the progression as soon as I took it. I could feel that I was leveling out and not going down that horrible hill. I am still pretty much ap t bound. BUT, I am happy to be where I am at right now. I tell my friends and family that I am now truly content and haapy. Don't get me wrong----I still have to have my home helper or I could not live on my own. I do have her and I have my computer so that I have my link to the outside world. I have hundreds of books that I read when I get tired of working on my book that I am writting. After having this MONSTER disease for 49 years now I have accepted it a long time ago. Cannot tell you when though. It was just there one day. When I was FINALLY diagnosed it was worth celebrating. At LAST I knew that there was a name for all the things that I had gone through. I will say that when I read it on a letter wrote to Social Security for my disability I cried for three weeks. After that I've never cried since. I thank the Lord each and every day for the LDN.

Hugs to all.

CJ"Faith sees the invisible, believes the incredible and receives the impossible."

[Guest guest]

hi aletha, i'm the one who asked you . david perlmudder is on the cutting edge of neurology! if he were on my plan, i would go to him. he is a big advocateof hyperbaric oxygen therapy which i personally question its validity and reliability but he is on the ball with alot of treatments. i take NAC which is a precursor to l-glutathione. your body cannot orally utilize straight l-glutathione buts its precursor NAC WILL CONVERT TO THIS ANTIOXIDANT. IT IS ALSO GREAT for bronchial infections. sorry- i hit the cap lock by mistake

Re: [low dose naltrexone] Liquid LDN

In a message dated 5/29/2005 3:02:40 AM Central Daylight Time, Aletha@... writes:

That is great CJ. I just didn't know enough about it in order to advise for it. Do you have to refrigerate it? Does the pharmacy turn it into a liquid solution, or do you?

Kind regards

Aletha

Yes, Aletha is has to be refrigerated. I mix a 50 mg pill with 50 ml of distilled water. ( I crush the 50mg pill and mix it myself with the water.) It works just great and I much prefer doing it this way and then I do not have to worry about fillers.

I have to say that I truly believe that the Lord lead me to the LDN website. I had just found out that I had three new huge lesions and what scared me the most was the big one on the brain stem. I knew that if I did not get something I was going to be a goner. I have had MS since I was 13 years old but I did not have my first major attack until July 11, 1988. After that I went slowly downhill. When I started the LDN I had nothing to lose and everything to gain. I researched it enough to know that I JUST HAD to get it and my neuro would not write me a script for it. So I had to take my health into my own hands. I will NEVER regret getting started on it. I was pretty much apt. bound and I had this huge fear of going into a nursing home. The LDN stopped the progression as soon as I took it. I could feel that I was leveling out and not going down that horrible hill. I am still pretty much ap t bound. BUT, I am happy to be where I am at right now. I tell my friends and family that I am now truly content and haapy. Don't get me wrong----I still have to have my home helper or I could not live on my own. I do have her and I have my computer so that I have my link to the outside world. I have hundreds of books that I read when I get tired of working on my book that I am writting. After having this MONSTER disease for 49 years now I have accepted it a long time ago. Cannot tell you when though. It was just there one day. When I was FINALLY diagnosed it was worth celebrating. At LAST I knew that there was a name for all the things that I had gone through. I will say that when I read it on a letter wrote to Social Security for my disability I cried for three weeks. After that I've never cried since. I thank the Lord each and every day for the LDN.

Hugs to all.

CJ"Faith sees the invisible, believes the incredible and receives the impossible."