RE: Mycoplasma pneumonia and LDN

[Guest guest]

Hi Liz,This past winter I had pneumonia. I know it's no fun and makes you feel HORRIBLE! I started taking LDN while I was still taking AVELOX for the pneumonia because I was anxious to do something to help me with MS. AVELOX is a very strong antibiotic which some people can't tolerate. I weigh 115 lbs. and medicines usually effect me pretty profoundly. I did fine on the AVELOX... I just made SURE I took it in the middle of a big meal. I had taken Arithromycin (z-pack) before the AVELOX but it didn't put a dent in the pneumonia.I hate to take antibiotics but in this case the pneumonia would probably have killed me. I'm thankful it was available. Also, I took probiotics and still do. I think it's fine to take the LDN along with antibiotics... all I can say is that it worked for me. Hope that helps. : )AnitaOn May 5, 2010, at 2:47 PM, wliz@... wrote:pneumonia

[Guest guest]

i've read reports of success with colloidal silver inhaled from a nebulizer

or spray mist bottle. drink lots also.

don't use it while on antibiotics as it's imcompatible with 4 families of

abx and research is needed to be sure what you're doing, so best to do one

or the other.

takes a lot, so little $25 bottles would run most people broke fast as you'd

need at least 8 oz/day... so make your own cheap and easy.

probiotics along with either abx or CS.

> [low dose naltrexone] Mycoplasma pneumonia and LDN

>

> Hi everyone

> I have just got a bloodtest that revealed I have high

> mycoplasma pneumonia antibodies. Recently I posted that I

> have been sick off and on for a couple of months, and I

> suspected that the LDN was dampening my immune system. I

> guess the pneumonia is what is underlying this problem.

> I will see my doctor tomorrow to figure out what treatment he

> recommends for the pneumonia, but I am also wondering if

> anyone here has experience with this? How does LDN work with

> this bacteria? Should I go off the LDN again? Thanks

>

>

[Guest guest]

Anyone suffering from mycoplasm should try to make contact with JAnice Seeley partner of Lindeman (who sadly dies this year) based in Cork COunty Ireland.

and JAnice use electro dermal screening for diagnostics and was involved in nosode

treatment to cure gulf war syndrome, and in mycoplasm in particular .

Some details -

These links are worthy of a look. See s article linked here on MS and BRucella ABortus BAng.

Nuala

Alliance of Registered Homeopaths : Find an ARH registered ...

Name, Janice Seeley, MARH. Address, Avalon, Derrycreigh, Glengarriff, County Cork, Eire (Republic of Ireland). Telephone, 00353 (0) 8790 94223 00353 (0) 8790 94223 ...www.a-r-h.org/FindMembers/findfb.php - Cached - Similar]

Download Issue - TPD422 New Pathways 33 (Page 2)

File Format: PDF/Adobe Acrobat - Quick ViewWritten with advice from homoeopath and electro-acupuncturist Lindeman. June's Story. June, age 55, from. Essex, worked as a jeweller, she was ...www.msrc.co.uk/downloads/npwm_2005_0033.pdf - Similar

A strange article by Lindeman - homeopath... - ten23 ... A strange article by Lindeman - homeopath and electro-acupuncturist - http://bit.ly/9wUFAA #ten23.friendfeed.com/.../strange-article-by-adrian-lindeman-homeopath - Cached

..

[Guest guest]

In addition to LDN and many other MS treatments, the MS page for " Patients Like

Me " has three really interesting threads on mycoplasma pneumonia presenting as

MS, then being treated with a " Combined Antibiotic Protocol " . Search the forun

the title in italics.

The wife's mycoplasma pneumonia has really really attacked her in a bad way.

They had to do an extensive search to find a physician to treat her sickness

with MANY antibiotics.

>

> Hi everyone

> I have just got a bloodtest that revealed I have high mycoplasma pneumonia

antibodies. Recently I posted that I have been sick off and on for a couple of

months, and I suspected that the LDN was dampening my immune system. I guess the

pneumonia is what is underlying this problem....

>

[Guest guest]

Mycoplasma is a " stealth pathogen " which used to be considered rather benign,

but after it was weaponized by the DOD & CDC, and tested on the US & Canada

populations some 30 to 50 years ago, it has become recognized as being very

dangerous. It has been identified by Drs. Garth & Nicolson as a likely

cause of Gulf War Syndrome, possibly as a contaminant in vaccines given to

troops. It gets into every part of the body & can mess up the central nervous

system & the immune system. It can be as devastating as Lyme. Not everyone who

gets it is damaged by it, & I'm sure many mild cases go unrecognized. But, to be

sure, I think it is a good idea to treat it aggressively and for a rather long

time.

I was hospitalized for two weeks in 1975 with mycoplasmal pneumonia, was off

work & on antibiotics for six weeks. After that, though I seemed to be cured, I

began to develop one auto-immune disorder after another, and ended up with

progressive fibromyalgia. I have been taking Monolaurin for about two years now,

because I don't want to be on antibiotics, but would, if I had an acute

infection, objectionable as that may be.

I'm not trying to scare you, only to suggest you do not take this lightly. Do an

internet search on " Mycoplasma stealth pathogen " & have a very serious

discussion with your doc, maybe even see an infectious disease specialist.

The Nicolsons wrote a " novelized " account of their research & experiences,

" Project Day Lily; An American Biological Warfare Tragedy " which can be bought

from them online. When I bought it, they were printing it up on order, one book

at a time.

Do NOT stop LDN. It can only protect your immune system, and might help prevent

long-term damage.

Best to you, & do keep us posted.

Konnie

>

> Hi everyone

> I have just got a bloodtest that revealed I have high mycoplasma pneumonia

antibodies. Recently I posted that I have been sick off and on for a couple of

months, and I suspected that the LDN was dampening my immune system. I guess the

pneumonia is what is underlying this problem.

> I will see my doctor tomorrow to figure out what treatment he recommends for

the pneumonia, but I am also wondering if anyone here has experience with this?

How does LDN work with this bacteria? Should I go off the LDN again? Thanks

>