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Re: Digest Number 992

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In a message dated 2/3/00 1:40:21 AM Eastern Standard Time,

lyme-aidonelist writes:

<< Message: 1

Date: Wed, 2 Feb 2000 18:27:06 EST

From: RMcmur3194@...

Subject: LETTER TO THE EDITOR-LYME DISEASE

Reid, that is a wonderfully stated letter. I really hope that the editor

can be unbiased and print this, or further yet, I hope that it sparks his

interest enough to do a follow up story. Thank you for writing it.

Your Lyme Friend,

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In a message dated 2/3/00 1:40:21 AM Eastern Standard Time,

lyme-aidonelist writes:

<< My son is 7 years old and has been suffering from joint paint throughout

his body. At first we thought it was JRA

but now we know it's Lyme Disease.

>>

Ree, I am sorry to hear that your son has Lyme at such a young age. For him

to be having arthritic symptoms means that he has had it for some time, so

don't let them tell you 3 or 4 weeks of abx is enough to cure him. There are

many people here that have children with Lyme and they are better equiped to

help you with particulars about children and Lyme. I wish you the best and

please keep us informed about how your son is doing and how his ya'll are

doing, too. This illness can and does effect the whole family and it is

especially hard when it involves our children.......makes your claws come out

to protect them.

Your Lyme Friend,

P.S. Welcome to the family !!!!!

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thanks michele i seem to do my best work when they piss me off with stupid

stuff lie that story....i ho[pe so too...watch the bastards try to sue me

.......will have to dig in archives for the back up but it was all true.....

Reid

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  • 4 months later...
Guest guest

Hi, all,

>I recall reading somewhere...I believe it was in 's, _Osler's

>Web_, that Dr. Byron Hyde said that there are only 4 other conditions

>(besides CFIDS) that are characterized by a low sed rate. One was

>hypergammaglobulinemia; I don't recall the others.

You're right: the diseases listed are :

ME = CFS

sickle-cell anemia

hypergammaglobulinemia (too much IgG)

hyper-fibrogenemia (too much fibrinogen)

hereditary sperocytosis (I think he means spherocytosis - round RBCs)

All (except maybe CFS) have a higher than normal concentration of big

proteins in the bloodstream - hemoglobin in sickle-cell and spherocytosis,

caused by hemolysis of abnormally shaped RBCs.

Jerry

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  • 10 months later...
  • 2 months later...
Guest guest

, you said it well the JRA road is tough but thanks to advances in the

medical arena isn't it wondeful to see and know children are fairing better

today than in the past. I know it does my heart good to see things looking up

in the area of JA! Parents , there is hope so hang tough and remember we all

understand and are here for you and the kiddos!!!

Donna Fox,

FACES Young Adult & Childrens Group

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Guest guest

>>>

From: " leah leah " <okieleah@...>

Subject: Re: recess time-mary s

-mary

what is on the list as being 1-4...sounds to me like

that principal

needs to

be fired....<<<

That topic makes me think back to when I was in

school, and corporal punishment was still being done.

( not that I think we need to go back to that mind

you... definalty not. ! ) ........ but it does

bring it to mind. I don't view having recess taken

away as so bad i guess when you can remember what

principal actions used to be. I see it on the same

lines as you can't have dessert if you don't eat your

dinner. I guess I am a strict disciplinarian. all my

kids had rules to follow.

Sherry

__________________________________________________

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Sherry,

I do not have any problem with taking recess away......if it changed the

behavior. I, too, am a strict diciplinarian.

One reason I homeschool my other son is that he would not behave for the

teachers and they were not nearly strict enough. They let him get by with

anything and everything. I don't. I know that it is not popular, but I

have spanked my kids. It worked for us. Except with Matt. No matter what

we do negatively, he does not respond by stopping the action. Never.

Ever. So why would we continue doing something that doenst' work. It is

time (After almost 11 long years) to admit that he needs something else.

(And who are the " slow " people here????)

Matt needs the social time. My arguement is " you dont' take Math away

because someone misbehaves because Math is needed. Well, for Matt,

socialization is desperately needed, much more than Math, so why should

we take it away? " I " ll just get it written in the IEP this year.

On Fri, 29 Jun 2001 07:27:20 -0700 (PDT) Sherry Edmonds

<sherryedmonds@...> writes:

> >>>

> From: " leah leah " <okieleah@...>

> Subject: Re: recess time-mary s

>

> -mary

> what is on the list as being 1-4...sounds to me like

> that principal

> needs to

> be fired....<<<

>

>

> That topic makes me think back to when I was in

> school, and corporal punishment was still being done.

> ( not that I think we need to go back to that mind

> you... definalty not. ! ) ........ but it does

> bring it to mind. I don't view having recess taken

> away as so bad i guess when you can remember what

> principal actions used to be. I see it on the same

> lines as you can't have dessert if you don't eat your

> dinner. I guess I am a strict disciplinarian. all my

> kids had rules to follow.

>

> Sherry

>

>

>

>

>

>

>

> __________________________________________________

>

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  • 1 month later...
Guest guest

Hi Paolo and Becky,

I was diagnosed with CMT back in 1976 at Mayo Clinic. Dr. Dyck did my nerve

biopsy and the diagnosis was CMT Type 2 of Dyck and Lambert. I know he is one

of the leading authorities on CMT and that since 1976 has added several new

classifications. I have been to several Neurologists in my past and only

found one to really confirm my symptoms and work with me. She retired and I

gave up on finding a new one. I have gone with my children to their

prospective new neurologist to find that things haven't change at all. One

told my daughter that there was no pain with CMT. I contradicted him with the

electrical shocks, the body aches compared to that of a high fever and the

muscle cramping. He also gave her another EMG and tried to tell her she had

Type 1. He had not seen the report from Mayo Clinic confirming Type 2. Two of

my children have been put in the wrong type of AFO's. I am now working again

to try and find a Doctor that will know something about CMT Type 2 and will

at least be able to work in a compassionate way with the four of us.

All of you have been such an encouragement to me. I know longer feel I carry

this alone. Thanks for the information on the Cylert drug.

of Indiana

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Guest guest

-----Original Message-----

From: flyingk@... <flyingk@...>

< >

Date: Thursday, August 02, 2001 8:04 AM

Subject: Re: [] Digest Number 992

>>>>>Hi , yes its sad but true things haven't changed much regarding

Dr's knowledge of CMT. BUT, its starting to change and as more is learned there

seems to be more interest on CMT since its so diverse and has so many different

genes causing the types to overlap or in some cases new mutations are being

found so more interest is being shown. And of course we can now map genes

better.

Have you tried the MDA for treatment? I know some here on out list uses them,

maybe they willl give you more information regarding MDA.

How old are your children? What symptoms do you/they have? Oh wow, the wrong

type of AFO! That can cause more problems then it could ever help! When

calling about for another Dr. ask if they have any other patients with CMT, if

the answer is no, don't make an appointment! When you find the answer yes,

make that appointment, LOL at least you will know in advance the Dr. has seen

at least one person with CMT! ~>Becky M.

Hi Paolo and Becky,

I was diagnosed with CMT back in 1976 at Mayo Clinic. Dr. Dyck did my nerve

biopsy and the diagnosis was CMT Type 2 of Dyck and Lambert. I know he is one

of the leading authorities on CMT and that since 1976 has added several new

classifications. I have been to several Neurologists in my past and only

found one to really confirm my symptoms and work with me. She retired and I

gave up on finding a new one. I have gone with my children to their

prospective new neurologist to find that things haven't change at all. One

told my daughter that there was no pain with CMT. I contradicted him with the

electrical shocks, the body aches compared to that of a high fever and the

muscle cramping. He also gave her another EMG and tried to tell her she had

Type 1. He had not seen the report from Mayo Clinic confirming Type 2. Two of

my children have been put in the wrong type of AFO's. I am now working again

to try and find a Doctor that will know something about CMT Type 2 and will

at least be able to work in a compassionate way with the four of us.

All of you have been such an encouragement to me. I know longer feel I carry

this alone. Thanks for the information on the Cylert drug.

of Indiana

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  • 1 month later...

Please give me an address... the Sam Gibbons, Federal Courthouse in Tampa has been declared a sick building. Some came from cross comtamination when we moved from the older building which was built in the 20's 4 years ago. I will send you information. GSA (General Services Administration) who manages most Govt buildings not doing anything substantial. A total of 5 courthouses in the Middle District of Florida have been found to have excessive amounts of molds and diesel fumes(Tampa) ... too long to explain on here. Tell me where to send.

Alycia Waller

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  • 11 months later...

charlene, not too be rude ,but I would do something about the litter box

thing that's not even funny!Can you move it somewhere so he can not see that

behavior anymore? That just goes too show kids do what they see! Maybe your

daughter wets herself,but at least she does'nt think she's an animal!

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I did get rid of the litter box and cats stay outside most of the

time as long as I ride the kids on the subject. I am sort of happy I do not

have to buy diapers anymore. The only thing now is to convert him to the

toilet. I dont think he thinks there is a difference between humans and

animals. My daughter had her weird behaviors too when she was 4 years old.

I assume this is just something that will be outgrown as long as I make

the cat box out of sight out of mind. We can not take these kids behavior

as extreme as we would a normal child. I have an aquaintence that his

daughter poopped on her aunts hood of the car.

charlene

-- Re: Digest Number 992

charlene, not too be rude ,but I would do something about the litter box

thing that's not even funny!Can you move it somewhere so he can not see that

behavior anymore? That just goes too show kids do what they see! Maybe your

daughter wets herself,but at least she does'nt think she's an animal!

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  • 4 weeks later...

ABA and TEACH?

It is said that " TEACCH " is the " kinder " therapy. I have colleagues who use

this approach or who teach in schools where this is applied (the operative

word) TEACH if I'm not mistaken the TEACCH approach is about organizing the

physical environment, developing schedules and work systems, making

expectations clear and explicit, and using visual materials have been

effective ways of developing skills and allowing people with autism to use

these skills independently of direct adult prompting and cueing ( as stated

on the website). It is interesting that instructors that use TEACCH don't

even realize that this is still Applied Behavior Analysis.

We behavior analysts, instructors or teachers of children with Autism use

schedules and use proactive manipulations of the environment as well. I have

always felt that many " different " approaches are just called something

different for it does not have the unfortunate negative connotation associate

with ABA by the general public.

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  • 3 months later...

--- Every summer we go to Denman Island. My parents have a summer

place there. I love the island.

In , " ekaraim

<cadchick@h...> " <cadchick@h...> wrote:

> How cool is that! I used to live in Qualicum! :)

>

>

>

>

>

> > Hi . I'm in Parksville, on Vancouver Island!

> > Kim

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,

You're kidding!!! I went to high school in Qualicum, grad '91. When

were you there? I also lived in Vancouver/Burnaby for 3 years, and

just moved back to this area 2-1/2 years ago.

Small world!

Kim

> > Hi . I'm in Parksville, on Vancouver Island!

> > Kim

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  • 3 years later...
Guest guest

First of all, i did have a flat mole around 2 mm round

on the upper right side of my nose which i always

" used " in my ID cards. Applying coconut oil on my

face every night slowly erased it (it would take quite

a while not overnight).

As to heating the oil, scrape it and directly apply on

your face at night. It would melt on your face as you

smother it around. Applying oil during daytime will

give you a tan when exposed to the sun.

> Message 2

> From: " bladeblah22 " bladeblah22@...

> Date: Sun May 7, 2006 2:32pm(PDT)

> Subject: New member here with questions about mole

> removal with coconut oil

>

> Hello everyone,

>

> I recently came across coconut oil via CureZone.com

> and learned that

> it's possible to remove moles, warts, acne, etc.

> with this

> incredible healing oil. I was very surprised to

> discover this and

> I'm eager to try it out.

>

> Here's my situation. I have about 20 or so small,

> flat moles on my

> face. There about the size of the end of a dull

> pencil point. Not

> big at all, just the amount of them is what bothers

> me. My goal is

> to cut down the amount of them to, at least, 12 or

> so. I'd be happy

> with that. If I could remove all of them, why not?

>

>>

>

__________________________________________________

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  • 5 months later...

Hi Hannah,

My name is Jasmine, i am nine years old, I have BPES, i am from mattawan,

MI. I'll be your friend. Where are you from? What grade are you in? BPES

makes me feel like I " m alone, stupid, and not pretty. How does it make you

feel? I like cheese!!! Please write me back soon.

- Jasmine

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