Guest guest Posted May 21, 2008 Report Share Posted May 21, 2008 Angie, Hi, I was trying to respond to your post. i have these websites that have many things you can change at home for easier breathing. Cleaners, mattress dust mite covers, air purifiers, all non-toxic which always helps relieve respiratory problems. The people there are also knowledgeable and can help you choose wha is right for you! Avoid harsh cleaners, perfumed detergents, dryer sheets, softeners, shampoo, conditioners as they all irritate your lungs. I do not know lung exercise unfortunately to help you there. However, the cleanest air is always at the beach. Only place I can breathe. Boost your immune system, I do not know if you can take Vit. C but I only drink Emergen-C, not tablets or pills, because buffered vitamin c is different. I also avoid the preservatives, additives, colorants or anything else artificial they may have. I also used to drink a lot of Rooibos, it is a tea from Africa which is higher in Antioxidants then Green Tea, tastes fantastic as well! My supplier was Mountain Rose Herbs online. All there stuff is checked and I have never had a problem with them. They also have GSE for boosting immue system. Always consult your Dr. Also very informative. http://www.alerg.com/?gclid=CPPhmsXDuJMCFQLBsgodQ2C-CQ http://www.greennest.com/testimonials.php God Bless !!! dragonflymcs Mayleen 02/07 ILD / MCS/ Fibro/ RADS/ TMJD/ AR +18 excercises to strengthe the lungs Any suggestions on things I can do to breathe easier and strengthe my lungs. thanks :)waheningmd <waheningmdaol (DOT) com> wrote: Dear All,I had an intake interview with the transplant group atColumbia-Presbyteri an last Friday. The good news was that myinsurance gave no issues at all (Blue Choice HMO -- self pay, now$800/month). I had mixed feelings that they seemed to indicate thatthey would now bring me in for the 3 days of tests -- somehow, I hadhoped that they would tell me to come back when I worse!! that, neverhaving used O2 except for exercise, I wasn't severe enough to meritfurther evaluation. The tests sound a little less intimidating than I had thought fromsome of the posts I've read (I dip in and out -- don't know how someof the regulars keep up with the hundreds of daily posts!!).The doctor whom I saw certainly seemed to make it quite clear to methat life post transplant was no bed of roses -- whether this is aroutine to scare away those not serious or the beginning of a hardeducation is unclear to me. But it seemed to be about as difficult alifestyle as that of someone on Aids maintenance therapy withintermittent setbacks.I would welcome any general or specific emails from those who havealready gone through transplant or are waiting for one.Wayne HeningNY/63/IPF 5/06 Angie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 22, 2008 Report Share Posted May 22, 2008 thank you very much !! : )dragonflymcs wrote: Angie, Hi, I was trying to respond to your post. i have these websites that have many things you can change at home for easier breathing. Cleaners, mattress dust mite covers, air purifiers, all non-toxic which always helps relieve respiratory problems. The people there are also knowledgeable and can help you choose wha is right for you! Avoid harsh cleaners, perfumed detergents, dryer sheets, softeners, shampoo, conditioners as they all irritate your lungs. I do not know lung exercise unfortunately to help you there. However, the cleanest air is always at the beach. Only place I can breathe. Boost your immune system, I do not know if you can take Vit. C but I only drink Emergen-C, not tablets or pills, because buffered vitamin c is different. I also avoid the preservatives, additives, colorants or anything else artificial they may have. I also used to drink a lot of Rooibos, it is a tea from Africa which is higher in Antioxidants then Green Tea, tastes fantastic as well! My supplier was Mountain Rose Herbs online. All there stuff is checked and I have never had a problem with them. They also have GSE for boosting immue system. Always consult your Dr. Also very informative. http://www.alerg.com/?gclid=CPPhmsXDuJMCFQLBsgodQ2C-CQ http://www.greennest.com/testimonials.php God Bless !!! dragonflymcs Mayleen 02/07 ILD / MCS/ Fibro/ RADS/ TMJD/ AR +18 excercises to strengthe the lungs Any suggestions on things I can do to breathe easier and strengthe my lungs. thanks :)waheningmd <waheningmdaol (DOT) com> wrote: Dear All,I had an intake interview with the transplant group atColumbia-Presbyteri an last Friday. The good news was that myinsurance gave no issues at all (Blue Choice HMO -- self pay, now$800/month). I had mixed feelings that they seemed to indicate thatthey would now bring me in for the 3 days of tests -- somehow, I hadhoped that they would tell me to come back when I worse!! that, neverhaving used O2 except for exercise, I wasn't severe enough to meritfurther evaluation. The tests sound a little less intimidating than I had thought fromsome of the posts I've read (I dip in and out -- don't know how someof the regulars keep up with the hundreds of daily posts!!).The doctor whom I saw certainly seemed to make it quite clear to methat life post transplant was no bed of roses -- whether this is aroutine to scare away those not serious or the beginning of a hardeducation is unclear to me. But it seemed to be about as difficult alifestyle as that of someone on Aids maintenance therapy withintermittent setbacks.I would welcome any general or specific emails from those who havealready gone through transplant or are waiting for one.Wayne HeningNY/63/IPF 5/06 Angie Angie Quote Link to comment Share on other sites More sharing options...
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