Good news about Glutathione

D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Sakem</b></i>

Where is this study published? Who conducted it? When?



I'm not feeling very confident that this is proof...first it was uncontrolled and very small group of subjs</end quote></div>

What the article left out was the names of who conducted the study which i read about in the "roundtable"..........
Alfred Visca,
Dr.Clark T. Bishop
Sterling C. Hilton
Valerie Hudson

Valerie and Dr. Bishop have been at the head of this right from the beginning. I have emailed them several times in the past and always got responses from both for info on Gsh before i took it initially 6 + years ago. I can only tell you from my experience it <b>DOES</b> work and <b>HAS</b> benefitted me greatly. I cant guarantee it will for everyone with cf but so far everyone i know with cf who has tried it has had good results. I dont need an official report to be done on everyone else to know what works for me. If you would like to do additional research on it i may be able to send you some links.
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Sakem</b></i>

Where is this study published? Who conducted it? When?



I'm not feeling very confident that this is proof...first it was uncontrolled and very small group of subjs</end quote></div>

What the article left out was the names of who conducted the study which i read about in the "roundtable"..........
Alfred Visca,
Dr.Clark T. Bishop
Sterling C. Hilton
Valerie Hudson

Valerie and Dr. Bishop have been at the head of this right from the beginning. I have emailed them several times in the past and always got responses from both for info on Gsh before i took it initially 6 + years ago. I can only tell you from my experience it <b>DOES</b> work and <b>HAS</b> benefitted me greatly. I cant guarantee it will for everyone with cf but so far everyone i know with cf who has tried it has had good results. I dont need an official report to be done on everyone else to know what works for me. If you would like to do additional research on it i may be able to send you some links.
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Sakem</b></i>

Where is this study published? Who conducted it? When?



I'm not feeling very confident that this is proof...first it was uncontrolled and very small group of subjs</end quote></div>

What the article left out was the names of who conducted the study which i read about in the "roundtable"..........
Alfred Visca,
Dr.Clark T. Bishop
Sterling C. Hilton
Valerie Hudson

Valerie and Dr. Bishop have been at the head of this right from the beginning. I have emailed them several times in the past and always got responses from both for info on Gsh before i took it initially 6 + years ago. I can only tell you from my experience it <b>DOES</b> work and <b>HAS</b> benefitted me greatly. I cant guarantee it will for everyone with cf but so far everyone i know with cf who has tried it has had good results. I dont need an official report to be done on everyone else to know what works for me. If you would like to do additional research on it i may be able to send you some links.
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Sakem</b></i>

Where is this study published? Who conducted it? When?



I'm not feeling very confident that this is proof...first it was uncontrolled and very small group of subjs</end quote>

What the article left out was the names of who conducted the study which i read about in the "roundtable"..........
Alfred Visca,
Dr.Clark T. Bishop
Sterling C. Hilton
Valerie Hudson

Valerie and Dr. Bishop have been at the head of this right from the beginning. I have emailed them several times in the past and always got responses from both for info on Gsh before i took it initially 6 + years ago. I can only tell you from my experience it <b>DOES</b> work and <b>HAS</b> benefitted me greatly. I cant guarantee it will for everyone with cf but so far everyone i know with cf who has tried it has had good results. I dont need an official report to be done on everyone else to know what works for me. If you would like to do additional research on it i may be able to send you some links.
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Sakem</b></i>
<br />
<br />Where is this study published? Who conducted it? When?
<br />
<br />
<br />
<br />I'm not feeling very confident that this is proof...first it was uncontrolled and very small group of subjs</end quote>
<br />
<br />What the article left out was the names of who conducted the study which i read about in the "roundtable"..........
<br />Alfred Visca,
<br />Dr.Clark T. Bishop
<br />Sterling C. Hilton
<br />Valerie Hudson
<br />
<br />Valerie and Dr. Bishop have been at the head of this right from the beginning. I have emailed them several times in the past and always got responses from both for info on Gsh before i took it initially 6 + years ago. I can only tell you from my experience it <b>DOES</b> work and <b>HAS</b> benefitted me greatly. I cant guarantee it will for everyone with cf but so far everyone i know with cf who has tried it has had good results. I dont need an official report to be done on everyone else to know what works for me. If you would like to do additional research on it i may be able to send you some links.
<br />
 
M

marcijo

Guest
Diane-I would be interested in where you get it, how much to take, etc as well. This may be something I want to try. Also-I am pacreatic sufficient-but it sounds like it would help my lungs as well? Thanks!
 
M

marcijo

Guest
Diane-I would be interested in where you get it, how much to take, etc as well. This may be something I want to try. Also-I am pacreatic sufficient-but it sounds like it would help my lungs as well? Thanks!
 
M

marcijo

Guest
Diane-I would be interested in where you get it, how much to take, etc as well. This may be something I want to try. Also-I am pacreatic sufficient-but it sounds like it would help my lungs as well? Thanks!
 
M

marcijo

Guest
Diane-I would be interested in where you get it, how much to take, etc as well. This may be something I want to try. Also-I am pacreatic sufficient-but it sounds like it would help my lungs as well? Thanks!
 
M

marcijo

Guest
Diane-I would be interested in where you get it, how much to take, etc as well. This may be something I want to try. Also-I am pacreatic sufficient-but it sounds like it would help my lungs as well? Thanks!
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>jersey</b></i>

hi Diane would you mind telling me what is the name of the product you take and what dose. I have been reading up on Glutathione aswell and am looking for info.

many thanks</end quote></div>

This is the one i take........

<a target=_blank class=ftalternatingbarlinklarge href="http://www.iherb.com/ProductDetails.aspx?c=1&pid=355
">http://www.iherb.com/ProductDe...spx?c=1&pid=355
</a>

here are some links to learn more of how it helps those of us with cf.......

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/gsh/layman_gsh.htm
">http://members.tripod.com/uvic.../layman_gsh.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/research/glutathione.htm
">http://members.tripod.com/uvic...glutathione.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://www.fda.gov/ohrms/dockets/ac/00/slides/3652s1_05/index.htm
">http://www.fda.gov/ohrms/docke...s1_05/index.htm
</a>

The recommended dosage (the protocol that was tested and used for years) is 30 mg per pound (of your weight) per day.
When i started taking GSH 6 years ago i was 114 lbs.
So my recommended dosage was 3420 mg. per day. Since you have to work up to your recommended dosage, i started out with 500 mg. twice a day for a week. I felt almost an immediate difference in my energy level. Next week i took 500 mg. 3 times a day for a week and so on till i got up to my recommended dose. I wound up getting sick a whole lot less, my pft's stabilized for a few years and i had the energy i used to have pre-cepacia. When i did get sick it was way less severe, and i recovered easily. I also gained weight and went up to 122 lbs. and kept it on. By the time i wzas up to full dose i was taking 1000 mg of oral GSH 4 times a day. I have to admit that is when i felt best.
Once i found out i had the fungus ball i stopped taking the GSH because someone told me it doesnt mix well with fungus, yeast etc. and sure enough i noticed the difference. no energy, loss of weight, feeling crappy like i used to........
I stayed off of it for a little bit but have recently gotten back on it after 2 hospitalizations and a bad summer. My Dr. suggested since i had done so well on it before, i should try half the doseage and see what results i get . That was in August and i have started gaining my weight back slowly, and my energy is returning. My fev1 went from 33% to 41% in a matter of less than 2 months. Unfortunately i did get sick again after that and did iv's at home and my pft's are back to 37%. Now that i have my energy i am active again, and can walk on my treadmill and will get those #'s back to where they should be ( mid 40's). I am now on a dose of 1500. per day and am going to up it to 2000 mg. a day.
If you need any more info, let me know............
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>jersey</b></i>

hi Diane would you mind telling me what is the name of the product you take and what dose. I have been reading up on Glutathione aswell and am looking for info.

many thanks</end quote></div>

This is the one i take........

<a target=_blank class=ftalternatingbarlinklarge href="http://www.iherb.com/ProductDetails.aspx?c=1&pid=355
">http://www.iherb.com/ProductDe...spx?c=1&pid=355
</a>

here are some links to learn more of how it helps those of us with cf.......

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/gsh/layman_gsh.htm
">http://members.tripod.com/uvic.../layman_gsh.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/research/glutathione.htm
">http://members.tripod.com/uvic...glutathione.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://www.fda.gov/ohrms/dockets/ac/00/slides/3652s1_05/index.htm
">http://www.fda.gov/ohrms/docke...s1_05/index.htm
</a>

The recommended dosage (the protocol that was tested and used for years) is 30 mg per pound (of your weight) per day.
When i started taking GSH 6 years ago i was 114 lbs.
So my recommended dosage was 3420 mg. per day. Since you have to work up to your recommended dosage, i started out with 500 mg. twice a day for a week. I felt almost an immediate difference in my energy level. Next week i took 500 mg. 3 times a day for a week and so on till i got up to my recommended dose. I wound up getting sick a whole lot less, my pft's stabilized for a few years and i had the energy i used to have pre-cepacia. When i did get sick it was way less severe, and i recovered easily. I also gained weight and went up to 122 lbs. and kept it on. By the time i wzas up to full dose i was taking 1000 mg of oral GSH 4 times a day. I have to admit that is when i felt best.
Once i found out i had the fungus ball i stopped taking the GSH because someone told me it doesnt mix well with fungus, yeast etc. and sure enough i noticed the difference. no energy, loss of weight, feeling crappy like i used to........
I stayed off of it for a little bit but have recently gotten back on it after 2 hospitalizations and a bad summer. My Dr. suggested since i had done so well on it before, i should try half the doseage and see what results i get . That was in August and i have started gaining my weight back slowly, and my energy is returning. My fev1 went from 33% to 41% in a matter of less than 2 months. Unfortunately i did get sick again after that and did iv's at home and my pft's are back to 37%. Now that i have my energy i am active again, and can walk on my treadmill and will get those #'s back to where they should be ( mid 40's). I am now on a dose of 1500. per day and am going to up it to 2000 mg. a day.
If you need any more info, let me know............
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>jersey</b></i>

hi Diane would you mind telling me what is the name of the product you take and what dose. I have been reading up on Glutathione aswell and am looking for info.

many thanks</end quote></div>

This is the one i take........

<a target=_blank class=ftalternatingbarlinklarge href="http://www.iherb.com/ProductDetails.aspx?c=1&pid=355
">http://www.iherb.com/ProductDe...spx?c=1&pid=355
</a>

here are some links to learn more of how it helps those of us with cf.......

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/gsh/layman_gsh.htm
">http://members.tripod.com/uvic.../layman_gsh.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/research/glutathione.htm
">http://members.tripod.com/uvic...glutathione.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://www.fda.gov/ohrms/dockets/ac/00/slides/3652s1_05/index.htm
">http://www.fda.gov/ohrms/docke...s1_05/index.htm
</a>

The recommended dosage (the protocol that was tested and used for years) is 30 mg per pound (of your weight) per day.
When i started taking GSH 6 years ago i was 114 lbs.
So my recommended dosage was 3420 mg. per day. Since you have to work up to your recommended dosage, i started out with 500 mg. twice a day for a week. I felt almost an immediate difference in my energy level. Next week i took 500 mg. 3 times a day for a week and so on till i got up to my recommended dose. I wound up getting sick a whole lot less, my pft's stabilized for a few years and i had the energy i used to have pre-cepacia. When i did get sick it was way less severe, and i recovered easily. I also gained weight and went up to 122 lbs. and kept it on. By the time i wzas up to full dose i was taking 1000 mg of oral GSH 4 times a day. I have to admit that is when i felt best.
Once i found out i had the fungus ball i stopped taking the GSH because someone told me it doesnt mix well with fungus, yeast etc. and sure enough i noticed the difference. no energy, loss of weight, feeling crappy like i used to........
I stayed off of it for a little bit but have recently gotten back on it after 2 hospitalizations and a bad summer. My Dr. suggested since i had done so well on it before, i should try half the doseage and see what results i get . That was in August and i have started gaining my weight back slowly, and my energy is returning. My fev1 went from 33% to 41% in a matter of less than 2 months. Unfortunately i did get sick again after that and did iv's at home and my pft's are back to 37%. Now that i have my energy i am active again, and can walk on my treadmill and will get those #'s back to where they should be ( mid 40's). I am now on a dose of 1500. per day and am going to up it to 2000 mg. a day.
If you need any more info, let me know............
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>jersey</b></i>

hi Diane would you mind telling me what is the name of the product you take and what dose. I have been reading up on Glutathione aswell and am looking for info.

many thanks</end quote>

This is the one i take........

<a target=_blank class=ftalternatingbarlinklarge href="http://www.iherb.com/ProductDetails.aspx?c=1&pid=355
">http://www.iherb.com/ProductDe...spx?c=1&pid=355
</a>

here are some links to learn more of how it helps those of us with cf.......

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/gsh/layman_gsh.htm
">http://members.tripod.com/uvic.../layman_gsh.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/research/glutathione.htm
">http://members.tripod.com/uvic...glutathione.htm
</a>

<a target=_blank class=ftalternatingbarlinklarge href="http://www.fda.gov/ohrms/dockets/ac/00/slides/3652s1_05/index.htm
">http://www.fda.gov/ohrms/docke...s1_05/index.htm
</a>

The recommended dosage (the protocol that was tested and used for years) is 30 mg per pound (of your weight) per day.
When i started taking GSH 6 years ago i was 114 lbs.
So my recommended dosage was 3420 mg. per day. Since you have to work up to your recommended dosage, i started out with 500 mg. twice a day for a week. I felt almost an immediate difference in my energy level. Next week i took 500 mg. 3 times a day for a week and so on till i got up to my recommended dose. I wound up getting sick a whole lot less, my pft's stabilized for a few years and i had the energy i used to have pre-cepacia. When i did get sick it was way less severe, and i recovered easily. I also gained weight and went up to 122 lbs. and kept it on. By the time i wzas up to full dose i was taking 1000 mg of oral GSH 4 times a day. I have to admit that is when i felt best.
Once i found out i had the fungus ball i stopped taking the GSH because someone told me it doesnt mix well with fungus, yeast etc. and sure enough i noticed the difference. no energy, loss of weight, feeling crappy like i used to........
I stayed off of it for a little bit but have recently gotten back on it after 2 hospitalizations and a bad summer. My Dr. suggested since i had done so well on it before, i should try half the doseage and see what results i get . That was in August and i have started gaining my weight back slowly, and my energy is returning. My fev1 went from 33% to 41% in a matter of less than 2 months. Unfortunately i did get sick again after that and did iv's at home and my pft's are back to 37%. Now that i have my energy i am active again, and can walk on my treadmill and will get those #'s back to where they should be ( mid 40's). I am now on a dose of 1500. per day and am going to up it to 2000 mg. a day.
If you need any more info, let me know............
 
D

Diane

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>jersey</b></i>
<br />
<br />hi Diane would you mind telling me what is the name of the product you take and what dose. I have been reading up on Glutathione aswell and am looking for info.
<br />
<br />many thanks</end quote>
<br />
<br /> This is the one i take........
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://www.iherb.com/ProductDetails.aspx?c=1&pid=355
<br />">http://www.iherb.com/ProductDe...spx?c=1&pid=355
<br /></a>
<br />
<br />here are some links to learn more of how it helps those of us with cf.......
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/gsh/layman_gsh.htm
<br />">http://members.tripod.com/uvic.../layman_gsh.htm
<br /></a>
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://members.tripod.com/uvicf/research/glutathione.htm
<br />">http://members.tripod.com/uvic...glutathione.htm
<br /></a>
<br />
<br /><a target=_blank class=ftalternatingbarlinklarge href="http://www.fda.gov/ohrms/dockets/ac/00/slides/3652s1_05/index.htm
<br />">http://www.fda.gov/ohrms/docke...s1_05/index.htm
<br /></a>
<br />
<br />The recommended dosage (the protocol that was tested and used for years) is 30 mg per pound (of your weight) per day.
<br /> When i started taking GSH 6 years ago i was 114 lbs.
<br />So my recommended dosage was 3420 mg. per day. Since you have to work up to your recommended dosage, i started out with 500 mg. twice a day for a week. I felt almost an immediate difference in my energy level. Next week i took 500 mg. 3 times a day for a week and so on till i got up to my recommended dose. I wound up getting sick a whole lot less, my pft's stabilized for a few years and i had the energy i used to have pre-cepacia. When i did get sick it was way less severe, and i recovered easily. I also gained weight and went up to 122 lbs. and kept it on. By the time i wzas up to full dose i was taking 1000 mg of oral GSH 4 times a day. I have to admit that is when i felt best.
<br />Once i found out i had the fungus ball i stopped taking the GSH because someone told me it doesnt mix well with fungus, yeast etc. and sure enough i noticed the difference. no energy, loss of weight, feeling crappy like i used to........
<br /> I stayed off of it for a little bit but have recently gotten back on it after 2 hospitalizations and a bad summer. My Dr. suggested since i had done so well on it before, i should try half the doseage and see what results i get . That was in August and i have started gaining my weight back slowly, and my energy is returning. My fev1 went from 33% to 41% in a matter of less than 2 months. Unfortunately i did get sick again after that and did iv's at home and my pft's are back to 37%. Now that i have my energy i am active again, and can walk on my treadmill and will get those #'s back to where they should be ( mid 40's). I am now on a dose of 1500. per day and am going to up it to 2000 mg. a day.
<br /> If you need any more info, let me know............
 
S

Sakem

New member
If this is from Valerie and Dr. Bishop then this is very old unoffical data. I wish they would conduct research on GSH and finally find out if it is benifical or not. 5 plus years ago my son was taking oral form, but we noticed no difference, and with not everything known about it's potential side effects, we stopped.

Not sure why they will not do and trials on it. I've heard they had started one, but then stopped because the proper procedures were not being followed. i've also heard that no one is willing to spend the money to do the research because this is not some type of drug that big drug companies could make lots of money from because it is sold over the counter....hmmm
 
S

Sakem

New member
If this is from Valerie and Dr. Bishop then this is very old unoffical data. I wish they would conduct research on GSH and finally find out if it is benifical or not. 5 plus years ago my son was taking oral form, but we noticed no difference, and with not everything known about it's potential side effects, we stopped.

Not sure why they will not do and trials on it. I've heard they had started one, but then stopped because the proper procedures were not being followed. i've also heard that no one is willing to spend the money to do the research because this is not some type of drug that big drug companies could make lots of money from because it is sold over the counter....hmmm
 
S

Sakem

New member
If this is from Valerie and Dr. Bishop then this is very old unoffical data. I wish they would conduct research on GSH and finally find out if it is benifical or not. 5 plus years ago my son was taking oral form, but we noticed no difference, and with not everything known about it's potential side effects, we stopped.

Not sure why they will not do and trials on it. I've heard they had started one, but then stopped because the proper procedures were not being followed. i've also heard that no one is willing to spend the money to do the research because this is not some type of drug that big drug companies could make lots of money from because it is sold over the counter....hmmm
 
S

Sakem

New member
If this is from Valerie and Dr. Bishop then this is very old unoffical data. I wish they would conduct research on GSH and finally find out if it is benifical or not. 5 plus years ago my son was taking oral form, but we noticed no difference, and with not everything known about it's potential side effects, we stopped.

Not sure why they will not do and trials on it. I've heard they had started one, but then stopped because the proper procedures were not being followed. i've also heard that no one is willing to spend the money to do the research because this is not some type of drug that big drug companies could make lots of money from because it is sold over the counter....hmmm
 
S

Sakem

New member
If this is from Valerie and Dr. Bishop then this is very old unoffical data. I wish they would conduct research on GSH and finally find out if it is benifical or not. 5 plus years ago my son was taking oral form, but we noticed no difference, and with not everything known about it's potential side effects, we stopped.
<br />
<br />Not sure why they will not do and trials on it. I've heard they had started one, but then stopped because the proper procedures were not being followed. i've also heard that no one is willing to spend the money to do the research because this is not some type of drug that big drug companies could make lots of money from because it is sold over the counter....hmmm
 
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