What's new
Cystic Fibrosis Forum (EXP)

This is a sample guest message. Register a free account today to become a member! Once signed in, you'll be able to participate on this site by adding your own topics and posts, as well as connect with other members through your own private inbox!

Curcumin tablets

anonymous

New member
Because Diane suggested you check out a little bit about Curcumin at this link: http://members5.boardhost.com/CFGSH/And Kylie put in her opinion about this web site, which is geared toward people taking glutathione!Jake
 

anonymous

New member
Good to hear you are benefitting from Glutathione Nate!You should share your story on the board....http://members5.boardhost.com/CFGSH/Jake
 

Diane

New member
Dave, I'm sorry my post opened a can of worms, I had a funny feeling it would, but i posted that link anyway, because it contained the answers you were looking for. I have to agree with what Nate said. If we sit around waiting for doctors and scientists to find a "cure", we will be waiting forever. Remember WE have the disease not them. We suffer from it, we feel the effects, and sometimes we have to be the ones to find our own answers when noone else can. I am not one to go out and just start taking something because someone told me to . I studied all about gsh before i started taking it and discussed it with my doctors. I came to the realization when i had to have two embolizations that if i dont do something NOW, RIGHT NOW, (other than sitting around and waiting for someone else to help my situation) by the time someone finally does find a way to help us, it may be way too late to make any difference. Lets face it, even if there was a "cure" by the time you have irreversible damage , a cure wont cure you. We cant turn back time, and reverse the damage thats already done. A cure will only stop more damage (hopefully). The only way to truely "cure" a genetic illness is to get rid of the faulty gene before the child is born, Once you are born with it, you are stuck with it. I dont think there will ever be a cure, BUT i do think there will be a treatment somewhere out there that will do amazing things for us. In the meantime while waiting for it, I am going to use whatever i can to maintain as much as i can of my life. Im sorry dave, for getting off track, but i felt i had to say all this...... ~ Diane 39 / cf / diabetes / b.cepacia
 

AbsintheSorrow

New member
I fully understand what you're saying. Doctors don't really care, they don't live with it. I just want to make sure you guys are aware that just because it's natural does NOT make it safe. They thought <i>natural</i> ephedra would be a GREAT way to lose weight... until it started killing people.
 

anonymous

New member
No problem Diane, I made another post on Glutathione. I am researching GSH now myself as I had never heard of the stuff until 2 days ago, so far I have some amazing stories and I am very interested in learning more so I will check the sites you suggested this weekend and I will discuss this with my doctor the next time I see him. Emily I disagree with anyone who says that the doctors don't care about you. I see the people at my cf center about 3-4 times a year and I have been going there for 9 years now and I am sure that your doctors have known you for a very long time and they know you pretty well. They want to see our health improve just as much as you do. So believe me they care. But in the most important aspect they are like everybody else you know, THEY DO NOT UNDERSTAND WHAT IT IS LIKE TO HAVE THIS DISEASE.Dave 29 w/cf
 

AbsintheSorrow

New member
No no I know my personal doctors care. I've seen the same pulmonologist for 10 years now, and she's awesome. I mean the people in charge of researching and trying to find a cure that don't actually see patients.
 

anonymous

New member
Hi DaveMy boyfriend has CF. He is 34 and he has started taking curcumin talets. We got turmeric with 95% curcumin extract from Planet organic, a health food shop in London. He has been on them for a few weeks. No major changes yet but he is looking good and hasn't got any worse. I will let u know how it goes. By the way, the medics always advise people not to take things until the clinical trials etc have been done. Well they would say that. It would be irresponsible if they didn't but both my boyfriend and I agree that it is worth the risk. Even tho these supplements might have side effects, CF has an even bigger side effect - death!! It might be too late for my boyfriend by the time they get round to OKing these things so we think it's worth the risk. Everyone has to make their own mind up. It's your body after all and sometimes the medic docs are working on tight budgets and long hours so they can't keep up with all the latest reseach.Good luck and hope you are feeling wellcaz
 

anonymous

New member
Kylie is not the only one banned from the GSH site. I was banned from the first site, (I am why they instituted the passwords), for simply asking if there were any negative results. I also went to V. Bishop's own Website guest list and found derogatory information on GSH. I simply asked for an explaination or clarification and was banished as a trouble maker. I have been following the GSH website for a long time, (the first site and the new site), and the people truly have faith in GSH. However, I would rather have documented results than "faith".Kylie is a bit too emotional, but she is not far off the mark.
 

anonymous

New member
really, i had no idea. kimandky@iinet.net.au if you want to talk...ah i wouldnt say emotional, i just feel very strongly about this topic ;D
 
Top