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Post by beckybailey on Nov 17, 2006 15:30:53 GMT -5
Zapping is very safe for children. I believe you hold them in your lap and zap the both of you at the same time. Considering the cost of things today, it is $180 very well spent. Send Ken at this website an email asking his opinion. zap.intergate.ca/Lots of people are zapping, but they don't all have the Ultimate Zapper. Unlike others, it works with extreme low frequency, square radio waves. There is nothing to do but hold the handles with damp paper towels and turn it on. No dials, nothing to learn (except hold the red handle with the right hand). Just be sure to use the electrical plug devices he sends with it, which has a GFI protector (if I said that correctly). If there was any surge or whatever, it flips off. Zapping has reduced my infestation to minimal. It is the number one thing that has helped me, and now I've added radionics which is zapping at it's highest level. And the infra-red sauna helps too, can't leave that out!
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Post by suebee on Nov 17, 2006 16:43:50 GMT -5
Yes Pez I've had this disease for over 20 years. It was up to three lesions on the back of my head. They just didn't want to heal so a biopsy was done. The doctor told me it was from stress and I was sure he was right because 20 years ago I was a type A person, always on the go with a basket too full. My home and poor kids were the cleanest in town, I say "poor kids" because I look back and wish all the time I spent cleaning had been spent playing with them. Now I can hardly take care of my own needs much less my home.
Anyway thoses lesions came and went, my back itched like crazy. Over the years I started having other symtoms, joint pain, chronic fatigue, a bit of crawling sensation, hands always dry and looked like paper cuts all over the tips and many medical problems. Nothing was so bad that I felt like I had something to be concerned about.
On Oct. 30, 2004 I was at my desk and my skin felt like I had bugs crawling all over me, not just my head and back, the stinging started from head to toe like a million bee's were on me. My skin looked like I'd been bite by something, had many raised bumps all over me. Because I was crying and going out of my mind, my husband put tape all over my back to prove nothing was there. Thats when we found all the fibers. I'm leaving a lot out because I'd end up writting a book, but yes I always say I got "Full Blown Mogellons" Oct. 04 My daughter just started getting lesions on her neck, chest, back and face. She has not got the crawling, stinging. I see her getting more and more fatigued but so far it's not a big problem.
I worry so much about my loved ones and friends. Even though they believe me i know they don't or can't understand the severity of this horror. I pray this CDC study is for real so that our love ones never have to live the horror of this disease. This disease is so unfair to the children, two of my three grandsons feel the crawling in their beds. Sometimes they wake up crying and tell there mom they want to sleep somewhere other than the bed. Children don't wake up out of a sound sleep because they are DOP and it makes my blood boil that they have to suffer with this. I also thank God that it's only at night and they can be happy little boys during the day. Their mom's head is loaded with lesions but she also seems to have a mild case.
It's hard to even suggest using products for them as my doctor's says, maybe we should let the sleeping dog, lay and not wake this horror up by treating it before it's full blown.
Maybe we have to be expoised to 3 or 4 things to get full blown? Who really knows? Not the CDC because they drag there feet at the expence of little ones.
I'm sure you'll get help from a lot of wonderful, smart folks in the group. I sure wish I could offer something to help. I'll keep her in my prayers. Love and good health to you, Sue in MD
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leighann
Full Member
Morgellon's - The point where Nature and Man collide...
Posts: 158
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Post by leighann on Nov 17, 2006 23:05:09 GMT -5
My Mom and sister have the most horrific case of this damn thing. However, I believe that I have a mild case. My sister has had to keep her head shaved and has been having such a bad time, I'm afraid that she will kill herself. My mother has almost all but cleared up except for a few places that just broke back out this week. I have been spending more and more time with them, and the other day my sister was having a REAL bad time, putting face masks, chrlorox and God know what else on her head, she was having a BAD time with some morgies coming out of her head and back, and it was so bad that while I was there, I have a couple of places break on my arm. (After leaving, I always shed my clothes I was wearing, separate from my other dirty clothes, take a shower, useing a coal tar solution (i.e. T-Gel, Denorex) as a body wash) but until now I didn't have this.
I know that when they get like this, I have to limit my visits. I believe that there are certain phases or levels of contagiousness. Also, my lesions seem to heal right up with no effort. That means that there is a certain amount of ability to fight this off.
But this also goes back to the factor of them being able to "communicate" to each other somehow. Why else would I be fine until I was around her when she was having such an outbreak? Who knows, anyway, thought I would throw that in.
Leigh Ann
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annb
Full Member
Posts: 109
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Post by annb on Nov 18, 2006 5:31:54 GMT -5
Pez,
My 4 children got morg at the same time I did. It took from 3 months to 2 years for my kids to be asymptomatic. They all differed in how their bodies dealt with it. I can't point to any one thing that helped them, as in the early days, I was trying everything. I am still suffering, they have only the mildest symptomsm very infrequently.
That my kids have cleared this is the only hope I have for myself.
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ukguy
Full Member
Posts: 193
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Post by ukguy on Nov 18, 2006 8:45:14 GMT -5
Hi Pez
I consider myself lucky as far as this condition goes.
I've had it for around 5 years and the symptoms over the last two years have been prettty much at a similar level.
I don't get lesions.
I do get:
The fibres, the white granular cells that look like worms with fibres in them, itching pretty much every day, crawling sensations/ bug attacks at night, stinging / pin prick sensations and the occasional thing out of my skin that looks like something from the X files.
And yep I count myself lucky.
No one else in my family seems to be affected by it.
Take care Ukguy
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linda
New Member
Posts: 0
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Post by linda on Nov 18, 2006 20:58:53 GMT -5
Hey there Pez,
I've had Morgs for ummmm...14 years now (on and off). In 2004, my 3-year-old son started showing symptoms. I'd always accepted that the fibers were just something weird my body did that stumpted the docs. Once I saw this all over my little boy, I had a huge wake-up call. Then, my baby girl showed signs; she was barely walking. She had it the worst. Looking back in hindsight, I realize that the strange fungus my older son had all over his back (that sparkled blue in the sunlight) had to have been Morgs and was probably the reason he always felt sick back then. Today, my kids have mild symptoms. My little girl still gets an itchy head, like me. Doxy once helped me. I also have no lesions, and I do not consider myself in terrible shape these days. My experiences lead me to believe that this is fungal in nature, but I might change my mind again next week. My boys are ADD/ADHD but are not being medicated. I can't help but wonder if the ADD/ADHD is caused by the Morgs since so many other kids with the Morgs have ADD. Today, I just try to live a healthy lifestyle; I try to stay happy to the best of my ability---you never know what horrors face you just around the corner. Of course you worry; you're a loving parent. Stay positive, eat right, love the hell out of your kids. Pray.
Take Care, Linda
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Post by friskers on Nov 18, 2006 22:32:08 GMT -5
When it hit me full blown 5 years ago i would have to say it was unbearable but now the past 2 years its been livable and Im able to work full time. I wouldnt say I live a "normal" life only because Im always worried about it getting worse so I sleep on air matress, bag my clothes, dont have cloth chairs or carpet ect ........... I think the most important factor is eating healthy and stepping up the immune system. No sugar, low carbs works for me :-*Frisk
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