Any thing Yet?

[honeybuns]

We are not taken seriously because our symptoms do not fit in the medical model. Just like those with Lyme disease were told they were either crazy or lazy for over 6 years. Some people with Lyme disease end up with pic lines in their hearts waiting in line to get strong antibiotics for a hope of a cure, because it has progressed to far.

Also, some people post that this is about "chemtrails", New World Order Plots, or a disease from Mars. It is simply a parasitic disease that is not in a textbook so just as in Lyme disease and countless other diseases patients are told they are delusional or some other BS.

I did not say anyone WAS a idiot. However, this parasite will lead to neurological damage. Doc Wymore of Oklahoma state tells of a man who was told to just stop scratching. Well the parasites ended up doing so much neurological damage that he was paralyzed and the lesions became worse. The longer you have these "bugs" (really worms) the deeper they go, they go into the muscle and you'll probably be wrongly diagnosed with Parkinsons or some other disease. But, once it has reached that point it is pretty much uncurable. You can easily feel your pancreas and tell that it is swollen. This is the first place they go. Then you begin to slowly lose night vision. The ringing in the ears is them in your ear.

However, it is obvious that people have a problem with reading comprehension. My first post I clearly stated that the horse meds were not the docs recomendation and people read that it was the doctors recomended.

I stated that the Horse Praziquantel (Biltricide) was better than the Human form because the fillers in the human form give you the ****s. I took enough to deworm a 1300 lb horse over several treatments with no side effects whatsoever. Your problem with the human form of praziquantel and lack of it working are that this is a highly resistant parasite and it needs much more than the average dose and several of them spread out 5 days apart.

So, it is either obvious that 1) the worm has affected peoples ability to read or thinking ability 2) that there are detractors on this group who do not have this disease and have there own agenda.

A person who will do anything to cure a disease is sane. Especially this horrible disease with very bad and irreversable (after a certain point) side effects. A kidney transplant last's average 10 years. about the 4th place these go is into the urinary tract. About the time they start eroding your hip bones.

If your allergic to sulfer use 35% food grade hydrogen peroxide mixed with water. And ozinated water. (but I doubt you actually have the disease from your comments)..

What I know is this. I had morgellons for over a year. After 1 month of treatment I have 0 (zero) black things comming out of my skin. No White (eggs) (Invermicin in the Equimax helps with that) and no more new lessions and the old ones are healing.

I don't care to find out the where's, why's, or to become facinated that this bug is a part of my life. I wanted it gone and it is! If you want to keep it , do so. You can buy a folder and document the effects yourself, until you lose your vision then you can use a tape recorder. It isn't my job to convince you. Get cured or die. It is your choice. If you want to wait for the salvation from a man in a lab coat be my guest.

But, beware that even accorning to the Journal of American Medical Association a doctor has a 16% chance at a correct diagnosis.
Also, according to the CDC, test's of people who we know have worms are very unreliable in finding them.

I'm not going to discuss it with you further. Since, obviously you will misread what I said as you did in the previous post.

What I'm using,
A Zapper (Hulda Clark) www.toolsforwellness.com
Vitamin C and Salt
Equimax (praziquantel and invermicin) ~ at higher than usual doses for my weight and a minimum of 7 treatments spread out 5 days apart.
and Parasite Cleans
Plus daily steam baths and the various lotions I've described earlier.

Even though I'm symptom free I will keep the treatment up for 7 weeks minimum.

I am symptom free. I've posted my pictures of the microfilia worms and coccoons. Even have had a full grown spider like thing come out of my skin as well as the red worms. No longer. I'm free ,

If you want to keep them then do so (IF YOU Actually have them!)..

some sites that might help.
www.lymephotos.com
www.lymebusters.com
www.toolsforwellness.com

You can buy a folder and document the effects yourself, until you lose your vision then you can use a tape recorder. It isn't my job to convince you. Get cured or die. It is your choice. If you want to wait for the salvation from a man in a lab coat be my guest.
But your probably a man in a lab coat that doesn't have the disease at all.

Like I said the reason people think we are crazy is because of the conspiracy theory sites, chem trail sites, genetic programming and all the other CRAZY things

AND

the same reason they though sufferers with Lyme disease were crazy until they discovered that it was an actual disease 6 years later. It isn't in there medical books. Look it says right here in this book the world is flat!! I don't have 6 years and neither do you. But, also after you have had this for awile you ARE crazy !! these get into your brain and leach neuropeptides.

A sane person WILL do anything to get cured. Especially knowing you eventually will infect your loved ones if you don't.
If you actually have the disease post some pictures and prove it.
there is a cure, I've given you enough info to cure yourself. I cured myself for less than the co-pay of your human drug with no side effects.

Be well or live in living hell. It is your choice.
I'm gone from this group.

[jano]

I have had this for over 10 years now. The only effect I have had is scarring and lesions that lasted for months at a time (a year was not unheard of). My mind is sharp and I am physically fit. The biggest pain in all this is the lesions. If I didn't have them - I would look at it as a crappy thing to have, but it would be better. I feel very fortunate in relation to others with this, but each individual is different in some faction or another.

I've had two near death experiences in my lifetime (one I went to the light and came back - which is a whole other story) and I am not about to go into panic mode doom and gloom over this. I know that whatever I have to live with, I am living and I also know that in a split second that can change. We all have different levels, views and tolerances in dealing with things - I know you are only trying to help, honeybuns, and we all know this sucks - we all have different tolerances of it - so I am not ready to become an evangelist to threaten anyone with what I think works, but I will share it.

[ladycolorado]

[quote=oregon ]
Hi, I would like to hear more about this treatment. I looked at the web site and see that the book is $125.00 that's a lot unless it realy works. Not that i have not spent a ton of money already. This is a hard fight, most things i have tried only seem to work for a short time, then stop working. God help us, I hope there is someting that realy works.
[/quote it is most interesting, i believe i have talked with this doctor myself on the phone myself. he is in florida right? i cannot discern if he is truly concerned or trying to make a buck, or both. yes i also think the book is prohibitively expensive. i did try the horse dewormer equimax on my lesion, he suggested it and did a little but not the cure all we hope for. i cannot gamble with ingesting poison. we are weak enough as it is, i do believe the wrong treatments may aggravate things or have severe health consequences. my hope lies not even in the cdc anymore (they could just sweep it under the rug). the best chance we have is perhaps with dr. karjoo in california, he is treating morgellons patients in santa ana california at no cost. he has the tools to research, he runs a doctors hospital and has another medical facility. he has said he wants to try to make a bloodtest to find morgellons and come up with a vaccine. he is a guest on shows of rense.com. yes most of us desperately wish to be normal. well its a good thing we have good friends who listen here.we will take our lemons and make lemonade out of the situation for now.there is hope, folks. at least is not fatal, i am thankful for that. and we can preserve ourselves.