posted
Anyone have information or experience with this. I have been having lung pain and shortness of breath for years. lately it has become very difficult just to breath. can hardly take a shower, no energy! Thanks, Health and Happiness, 44
Posts: 34 | From Prescott, AZ | Registered: Aug 2004
| IP: Logged |
posted
This is a roundworm that is not detected in the "normal way" but can be seen in lung fluid. Researchers in CA,have found it to be present in up to 70% of people diagnosed with CFS. Any one know of this? Peace,44
Posts: 34 | From Prescott, AZ | Registered: Aug 2004
| IP: Logged |
lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
You need to talk to gayle on parasite thread. Its here. I ll try to bring it up top
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
| IP: Logged |
lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
Many others on para thread can help too
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
| IP: Logged |
posted
Thanks everyone! I have seen a pulmonologist and have had numerous lung ex-Rays. Everything always looks "normal" It is not! I am seeing a new Dr. and she is doing more tests. Hope something shows up! Thanks again, 44
Posts: 34 | From Prescott, AZ | Registered: Aug 2004
| IP: Logged |
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149
posted
You need to treat for parasites. I am loaded with these worms too. You can search and search for tests and doctors, but the tests suck, doctors are clueless, and the worms are still there.
Find someone who treats parasites, preferably a Dr. K type of doc, as they know they are real and know lyme patients are loaded with them.
In the interim, you might want to check out the salt/c protocol with herbs on the parasite warrior's thread.
-------------------- --Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together). Posts: 5418 | From earth | Registered: Mar 2011
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic