Please Read! Help Needed Here....

[Baraka Obam]

See that one red dot, it looks like somthing that started forming on the body VERY early on for me. These red spots some nearly flat but most had a raised round dome like thing. These are tough and can not be picked away, if they are broken they will not bleed profusely like the lesion skin vein blood spot. They are different. The color of the bright red dot DOES match the inside material of the lesion though!!! I took a red hot pin and burst every one of these red dots on my body, the less there is the less there will be. In fact now that I think about it, the first systemic problem that showed was these red spots, they were just exactly where my devil horns should have been, thats a fact. Funny how things come back.

What part of the baby are we looking at here, some of these spots or red dots may just be broken capillary, if this is your grand baby kritters it is still a wait and see thing, hopefully the baby's immune system will kick in and take care of it for this childs whole life. My daughter was born with it, she still looks great, when she was younger she had keratosis all over the back of her arms and some small growths. I had them cut off but the doctor idiot did not cut them all, now they have spread.

[Kritters]

NO! Baraka fearless leader....it is a child I don't even know!!! Please read the post!! This child is one of a twin and after a flu shot became like this.

I don't know these people. Please, everyone...READ THE FREGGAN POST!! iT'S NOT ABOUT ME OR MINE...IT'S ABOUT HER AND HERS!!!! hER BABY IS PARAPLEGIC!!

PLEASE JUST READ IT!

XXOXOXO
kRITTS

[Kritters]

don't know Kam....
I think about 11 or so. no...I don't believe so.
Can you check out the website?

she's one of a twin and the other had violent reacton to flu shot, but this one is a freaking paraplegic.

xoxo
Kritts

[Kritters]

So, what is this....the Kritters and Kammy show?

NO one has anything to offer to this chld?

Hello....is this the family I thought rallied to help?

[-----------]

Darn it, Kritts, it's late and I'm tired. I don't see a weblink to a site. On the first page there's a bad link to a YouTube?

I need to go to bed...wake up tomorrow and try again.

[sarothra]

Originally Posted by Kritters

This child has Morgellons.

These are nematode tracks, after a major "hatch-out" -

This happened to me. I had been fighting a big lesion on my stomach but couldn't get it to go away. It lasted for months. Suddenly over a period of several days the lesion started to get more red, swollen and spread out. I realize now that the larva had developed and the worms were exiting the lesion.

The nematodes then traveled down through my groin (very painful), with many ending up in my right foot. My foot (just my right one) is very swollen and I can feel the hard nematode heads up near the toes. There are more in the ankles too. I'm trying to crush them but the foot is so swollen I can't get to them so these nematodes just keep growing.

I've used the pulsating massager but am unsure of results of that.

Sadly, you can't crush the nematodes on a child, but I'm sure there are lots of other helpful techniques. I would try a high salt diet, low sugar (or no sugar preferably) - DE on any possible lesions and the anal area. These are just a few suggestions, but my forte is really the direct kill.

I have 2 toddler who are infected but who have no lesions. I think I am the infectious agent so my agenda is to get my lesions under control and GONE and then I think theirs (I hope) will go away or lessen considerably. They are already much better since I have started my protocol.

I also use the vitamin C/salt but have a terrible diarrhea reaction so have to modify it down to where I can handle it.

sar

[dizzy dame]

Kritts, I am so sorry about this child. I read the post but didn't have anything to offer in the way of help.

I have just finished doing the humaworm that Kat wrote about though, and I also ordered and use the cream from that site. I will say that the cream really helped my skin. It cleared up some spots for me really fast.

I am taking a lot of other natural herbs too, but I think the humaworm did some good. I also take the DE. I am not sure what is helping but things have gotten much better.

I hope someone can help this child. Prayers going out for her...XO DD

[Kritters]

Originally Posted by Kritters

Everyone,
I don't know if any of you get any newsletters from this site, "Andalusian Dogs" but please read this. this poor child is basically paralyzed. Maybe we can help"
xoxoKritts

Andalusian Dogs Presents: Under The Eightball

http://www.youtube.com/v/Lq6qotHIiCM&hl=en&fs=1&



Andalusian Dogs
show details 3:22 PM (25 minutes ago) Reply



Friends, I have come across a story of a brave soul. A girl, who's story is so similar to Lori's, the only difference is that she is too young to diagnose with ALS. "ALS" sufferers are processed and stamped and pushed out of the medical community to somehow come to peace with death. This is the worst form of these horrible infections which continue to be ignored. Please, I beg for myself and for her mother Lori, if you have any information that can ease the last 4 years of hell on earth for this family please contact us. Below is a short description and a youtube video that the family assembled. You can contact Lori, Alex's mother at alexsarmy@hotmail.com

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In spring of 2005, Alex began having difficulty with movement of her left arm. At the time, she was in the middle of softball season, enjoyed riding horses, and playing with her friends. In late May, she noticed her left leg started to lag behind. We thought the worst. We went to Omaha where she tested positive for Mycoplasma pneumoniae and started monthly intravenous immunoglobulin treatments, or IVIg's. At first they told us it was Guillian Barre Syndrome, but then decided it wasn't. Unfortunately, the condition progressed. We then followed up at Mayo Clinic in August, but this time they gave us a diagnosis of motor neuron syndrome. The treatments they prescribed didn't seem to help either and we were off again- this time to St. Paul, MN. Things weren't so clear after all of the tests as the neurologist there seemed to be unsure of a diagnosis. She did test negative to SOD1 and SOD2 genes where they told us this can go along with ALS. All other genetic testing has been negative. We continued IVIg's. Then, in November, 2005, we journeyed to Houston, TX to an immunotoxicologist. Even though there were significant amounts of stachybotrys mold and other mycotoxins in Alex's blood, the treatment remained the same, and we continued on with, this time, weekly IVIg treatments. We left our house and everything in it to get out of the environment that may have been causing this to Alex. She also tested positive to acetylcholine receptors there as well which we thought could go along with myasthenia gravis.
Unfortunately, she progressed further and the paralysis went to her right side. In December, she lost her ability to walk. In January, 2006, we were off again to Springfield, MO where she was clinically diagnosed and tested positive for Lyme Disease, (although the test performed was not FDA-approved). She recently tested positive for a common co-infection associated with Lyme Disease called Bartonella. Later, (approximately in 2007-2009) we would also discover several heavy metals in her body such as mercury, nickel, aluminum, cadmium, and tungsten. Arsenic in her hair sample. Her condition continued to worsen and started to affect her breathing muscles. On February 23, 2006, doctors told her she wouldn't make it through the night.

She did make it...and she is still with us. On March 14th, we air-lifted her to Omaha, NE where shortly thereafter, she had a tracheostomy-ventilator and G-tube inserted. We spent the next 5 months in 3 different hospitals.

We still search for a compassionate and passionate Drs to help seek a diagnosis. Everyone we write chose to ignore Alex. We have struggled to find the help Alex deserves to help save her life.

A Dr in Colorado who was misdiagnosed with ALS and was positive with lyme flew to Alex and clinically diagnosed her with lyme as well. This Dr has since reitred.
She did test positive for HHV-6 (virus) and pro-inflammatory markers were all normal. There are so many confusing things about Alex's illness which makes it so difficult to proceed with proper treatment. Alex has lost the ability to speak and she can no longer swallow. She can commnicate by twitching the corner of her mouth to yes questions. All of her nutrition is through a tube in her stomach. In the fall of 2008, she was tested for more motor neuron testing which the Dr's were confident would be abnormal but came back negative. She also tested negative to Tay-Sachs disease. All neuromuscular genetic testing has been negative.
Dr's we have spoke with believe this stemmed from 1 of 3 things: genetic, a toxin, or a virus. Since Alex has an identical twin and all genetic testing has come back normal we believe it is one of the other 2.

Today, after 4 horrifying years Alex continues to fight everyday with her heart and soul praying someone can help her figure out this mystery and nightmare.
If we only knew for sure what was causing this, we would know how to fight it, but nobody will take the time and effort to commit to help her.

In sending her mom information about metal toxicity, mold and neurological damage, I came across this website and thought I'd share with you if you haven't seen it. I signed up for the newsletter and was given a free download for what looks to be a good book written by an entepreneur who cured himself from diseases like ours...which you can also download if you sign up. From Kammy's thread, back to here, I want to mention again that it's interesting this little girl tested positive for Lyme and became this ill and neurologically impaired after vaccines. Who knows which came first or together, but I find it curious.

Kritts
10 Common Causes of Chronic Conditions: Cause #7

[Kritters]

That website also contained a source to find mercury-free dentists!
Mercury Free Dentists
Kritts