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A little glutathione goes a long way!!!!

L

lilismom

Active member
Mandy,
I'm so glad to hear inhaled GSH is working so well for you! Thanks for the updates on the Denufosal trial.
 
L

lilismom

Active member
Mandy,
I'm so glad to hear inhaled GSH is working so well for you! Thanks for the updates on the Denufosal trial.
 
L

lilismom

Active member
Mandy,
I'm so glad to hear inhaled GSH is working so well for you! Thanks for the updates on the Denufosal trial.
 
L

lilismom

Active member
Mandy,
I'm so glad to hear inhaled GSH is working so well for you! Thanks for the updates on the Denufosal trial.
 
L

lilismom

Active member
Mandy,
I'm so glad to hear inhaled GSH is working so well for you! Thanks for the updates on the Denufosal trial.
 
R

rvm1212

New member
Thank you very much for the information
I hope they will find patients to participate on the trial.
As for NAC, my boyfriend is currently on acetylcysteine 1200 a day (fizzy tablets), for your post I asume that is NAC. He is doing really good since he is on it. Although I am not sure if is due to acetylcysteine or because he is on a higher dosis of inhaled steroids. He used to cough pretty much in the morning and now he doesn´t cough at all. His sputum is white and he just brings up a little bit with chest therapy. He is thinking on getting a higher dose since his neumologyst told him it would be safe to take 1800/day. We are looking foward to see his ptf, (october), although we don´t know if we´ll see much improvement since his baseline is very good (FEV and FVC on the 90íes).
I would like to know how other people on NAC are doing.
Rita. Boyfriend CF diagnosed this year at 35
 
R

rvm1212

New member
Thank you very much for the information
I hope they will find patients to participate on the trial.
As for NAC, my boyfriend is currently on acetylcysteine 1200 a day (fizzy tablets), for your post I asume that is NAC. He is doing really good since he is on it. Although I am not sure if is due to acetylcysteine or because he is on a higher dosis of inhaled steroids. He used to cough pretty much in the morning and now he doesn´t cough at all. His sputum is white and he just brings up a little bit with chest therapy. He is thinking on getting a higher dose since his neumologyst told him it would be safe to take 1800/day. We are looking foward to see his ptf, (october), although we don´t know if we´ll see much improvement since his baseline is very good (FEV and FVC on the 90íes).
I would like to know how other people on NAC are doing.
Rita. Boyfriend CF diagnosed this year at 35
 
R

rvm1212

New member
Thank you very much for the information
I hope they will find patients to participate on the trial.
As for NAC, my boyfriend is currently on acetylcysteine 1200 a day (fizzy tablets), for your post I asume that is NAC. He is doing really good since he is on it. Although I am not sure if is due to acetylcysteine or because he is on a higher dosis of inhaled steroids. He used to cough pretty much in the morning and now he doesn´t cough at all. His sputum is white and he just brings up a little bit with chest therapy. He is thinking on getting a higher dose since his neumologyst told him it would be safe to take 1800/day. We are looking foward to see his ptf, (october), although we don´t know if we´ll see much improvement since his baseline is very good (FEV and FVC on the 90íes).
I would like to know how other people on NAC are doing.
Rita. Boyfriend CF diagnosed this year at 35
 
R

rvm1212

New member
Thank you very much for the information
I hope they will find patients to participate on the trial.
As for NAC, my boyfriend is currently on acetylcysteine 1200 a day (fizzy tablets), for your post I asume that is NAC. He is doing really good since he is on it. Although I am not sure if is due to acetylcysteine or because he is on a higher dosis of inhaled steroids. He used to cough pretty much in the morning and now he doesn´t cough at all. His sputum is white and he just brings up a little bit with chest therapy. He is thinking on getting a higher dose since his neumologyst told him it would be safe to take 1800/day. We are looking foward to see his ptf, (october), although we don´t know if we´ll see much improvement since his baseline is very good (FEV and FVC on the 90íes).
I would like to know how other people on NAC are doing.
Rita. Boyfriend CF diagnosed this year at 35
 
R

rvm1212

New member
Thank you very much for the information
I hope they will find patients to participate on the trial.
As for NAC, my boyfriend is currently on acetylcysteine 1200 a day (fizzy tablets), for your post I asume that is NAC. He is doing really good since he is on it. Although I am not sure if is due to acetylcysteine or because he is on a higher dosis of inhaled steroids. He used to cough pretty much in the morning and now he doesn´t cough at all. His sputum is white and he just brings up a little bit with chest therapy. He is thinking on getting a higher dose since his neumologyst told him it would be safe to take 1800/day. We are looking foward to see his ptf, (october), although we don´t know if we´ll see much improvement since his baseline is very good (FEV and FVC on the 90íes).
I would like to know how other people on NAC are doing.
Rita. Boyfriend CF diagnosed this year at 35
 
P

PeterC

New member
dramamama:

You continue to impress me with your determination, compassion and high quality of knowledge you so willingly share with all of us!

Your posts are always informative and in my opinion, among the most valuable posts on this site.

No nonsense, accurate, clear, compassionate etc, etc...

Thanks again for providing me with useful, timely information!!!

Your continued commitment and hard work helps to make this forum the best place for all people with CF concerns to come to when they want to be more fully updated and educated.

Fabulous as usual!!!
Sincerely:
PeterC 58 soon to be 59 w/cf diagnosed at age eight.
 
P

PeterC

New member
dramamama:

You continue to impress me with your determination, compassion and high quality of knowledge you so willingly share with all of us!

Your posts are always informative and in my opinion, among the most valuable posts on this site.

No nonsense, accurate, clear, compassionate etc, etc...

Thanks again for providing me with useful, timely information!!!

Your continued commitment and hard work helps to make this forum the best place for all people with CF concerns to come to when they want to be more fully updated and educated.

Fabulous as usual!!!
Sincerely:
PeterC 58 soon to be 59 w/cf diagnosed at age eight.
 
P

PeterC

New member
dramamama:

You continue to impress me with your determination, compassion and high quality of knowledge you so willingly share with all of us!

Your posts are always informative and in my opinion, among the most valuable posts on this site.

No nonsense, accurate, clear, compassionate etc, etc...

Thanks again for providing me with useful, timely information!!!

Your continued commitment and hard work helps to make this forum the best place for all people with CF concerns to come to when they want to be more fully updated and educated.

Fabulous as usual!!!
Sincerely:
PeterC 58 soon to be 59 w/cf diagnosed at age eight.
 
P

PeterC

New member
dramamama:

You continue to impress me with your determination, compassion and high quality of knowledge you so willingly share with all of us!

Your posts are always informative and in my opinion, among the most valuable posts on this site.

No nonsense, accurate, clear, compassionate etc, etc...

Thanks again for providing me with useful, timely information!!!

Your continued commitment and hard work helps to make this forum the best place for all people with CF concerns to come to when they want to be more fully updated and educated.

Fabulous as usual!!!
Sincerely:
PeterC 58 soon to be 59 w/cf diagnosed at age eight.
 
P

PeterC

New member
dramamama:

You continue to impress me with your determination, compassion and high quality of knowledge you so willingly share with all of us!

Your posts are always informative and in my opinion, among the most valuable posts on this site.

No nonsense, accurate, clear, compassionate etc, etc...

Thanks again for providing me with useful, timely information!!!

Your continued commitment and hard work helps to make this forum the best place for all people with CF concerns to come to when they want to be more fully updated and educated.

Fabulous as usual!!!
Sincerely:
PeterC 58 soon to be 59 w/cf diagnosed at age eight.
 
T

TwistedTanya

New member
Has anyone done or know of doing glutathione with the eFlow? I was taking the oral GSH and it seemed to help but then I started getting nauseated. Has anyone else had this problem?
 
T

TwistedTanya

New member
Has anyone done or know of doing glutathione with the eFlow? I was taking the oral GSH and it seemed to help but then I started getting nauseated. Has anyone else had this problem?
 
T

TwistedTanya

New member
Has anyone done or know of doing glutathione with the eFlow? I was taking the oral GSH and it seemed to help but then I started getting nauseated. Has anyone else had this problem?
 
T

TwistedTanya

New member
Has anyone done or know of doing glutathione with the eFlow? I was taking the oral GSH and it seemed to help but then I started getting nauseated. Has anyone else had this problem?
 
T

TwistedTanya

New member
Has anyone done or know of doing glutathione with the eFlow? I was taking the oral GSH and it seemed to help but then I started getting nauseated. Has anyone else had this problem?
 
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