Keebler, as usual you are my angel sometimes. I went searching for info on myself and mycoplasma and it wasn't until I read your thread from '16....
that I got smacked in the forehead.
This report is so worth a read and a save for so many. Thanks Keebler!!!!!
Pam
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6489 | From Louisville, Ky | Registered: Jan 2002
| IP: Logged |
I've read - maybe it was in the book, Lab 257(?), that borrelia bacteria were mixed with mycoplasma and brucellosis - ie weaponized.
Posts: 13151 | From San Francisco | Registered: May 2006
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Pam,
Glad you found that. Hey, likely, I lifted that from someone else down the line as generally I just pass along what I've seen that hits a good chord. The real work is done by Garth Nicolson, such a top researcher - but I'm glad we have LymeNet so that we can share good works.
And the article's author, by Scott Forsgren, has been a gold mine of information for me. He's amazing at gathering and sharing.
It's all so startling, though, as it seems most typical doctors have no clue to the complexities of such chronic stealth infection. The more sharing we can do, the better.
I would hope that anyone, everyone, would share any links at the appropriate time / place. Share, share, share. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
Rivendell
Frequent Contributor (1K+ posts)
Member # 19922
posted
Hi Pam, Robin, and Keebler,
I've seen that article and read some of it before (concentration not as good as it used to be).
So ridiculous that we experiment on people.
But I have been dealing with mycoplasma, and it is a bugger to get rid of - just like the other infections.
I've had good luck with collodial silver nasal spray (the name starts with an "a" - I'm a bit foggy today) and also using essential oils mixed with coconut oil and rubbed on my body.
Zithromax helps, but when I go off of it, the mycoplasma tends to come back.
Mine is mycoplasma pneumonia, though we likely have other forms which are not included in the testing.
map1131
Frequent Contributor (5K+ posts)
Member # 2022
posted
Hi Rivendell!
I've tested highly positive for mycoplasma pn a few times. I rifed for it off and on some years ago.
But I never had any typical myco pn sx as lungs and other breathing passages were never one of my issues.
Three months ago I started seeing a Naturopath who uses Biofeedback and GB4000. I just wanted the biofeedback info. Candida, Mycoplasma, Parasites need to be worked on.
I haven't had Lyme, Bart or Babs sx to deal with for at least 6 mths. But my gut is a mess and still dealing with fatigue.
Mycoplasma is very much a part of my issues. I started using rife freq that truly hit Myco and there is a huge reaction. But not a herx that I can't handle.
Onward it is! I'm getting there.
Pam
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6489 | From Louisville, Ky | Registered: Jan 2002
| 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