Patricia B3749
New member
Hello Everyone.
Just wanted to post an update about my autologous stem cell treatment for COPD. I traveled to Florida on May 5th, then on May 7th met with Dr F, he explained every detail of what he would be doing. Next step was for me to receive an infusion of my own stem cells by intravenous, it took about one and one half hour. The next day I went back to Dr F and received a nebulizer treatment of glutathione and retinoic acid, and that was all there was to it. The first couple of days my breathing was a bit more labored than normal but I have to say that since I came back home I have noticed an increase in my energy level. I have not stopped using oxygen, but I find myself taking the cannula out of my nose and holding it in my hand, I am able to complete small tasks without taking a break, which is something I was unable to do before. I must tell you that I have end stage COPD in both lungs, top and bottom, very severe so these small changes mean a lot to me however long they last. It will be a few months before we know the full benifits of treatment , I am planning another treatmment in six to nine months from now. I have a small income and I know that many of you do also, so for me Dr F is a wonderful caring doctor, whose treatments are affordable. I will keep posting progress and for all of you out there stay positive.
Patricia B3749
junior member
stem cell treatment
May,5th 2010,
Just wanted to post an update about my autologous stem cell treatment for COPD. I traveled to Florida on May 5th, then on May 7th met with Dr F, he explained every detail of what he would be doing. Next step was for me to receive an infusion of my own stem cells by intravenous, it took about one and one half hour. The next day I went back to Dr F and received a nebulizer treatment of glutathione and retinoic acid, and that was all there was to it. The first couple of days my breathing was a bit more labored than normal but I have to say that since I came back home I have noticed an increase in my energy level. I have not stopped using oxygen, but I find myself taking the cannula out of my nose and holding it in my hand, I am able to complete small tasks without taking a break, which is something I was unable to do before. I must tell you that I have end stage COPD in both lungs, top and bottom, very severe so these small changes mean a lot to me however long they last. It will be a few months before we know the full benifits of treatment , I am planning another treatmment in six to nine months from now. I have a small income and I know that many of you do also, so for me Dr F is a wonderful caring doctor, whose treatments are affordable. I will keep posting progress and for all of you out there stay positive.
Patricia B3749
junior member
stem cell treatment
May,5th 2010,