Re: Digest Number 1441

[Guest guest]

I have to agree with Jane, you dont want to exceed your bodies limitations

on any meds, I also get a CBC and liver function test done bi-weekly. And

weekly when I was on IV. Plus there are drug counter interactions with meds

you already might be taking. Play it safe, ask your Dr! You may have bad

side effects even with herbal remedies! Patience is something we all have to

acquire, Lyme in the later stage (long time illness) , will take a long time

to overcome, and may not be complete. Please be careful, this message is for

everyone that hastily ignores the safety of their own quick fix idealism.

Take care all, Bill

Re: [ ] Digest Number 1441

>

>

>In a message dated 9/2/00 3:35:30 AM, egroups writes:

>

><< My doc has ordered it and I got it but the druggist said it was

>forgout---I don't have gout. Could it be for joint pain? Also, oneother

>question---I am taking amox 4x a day, probenicid 3x a day asper docs

>orders---I am considering adding Tini 500mg 3 x a day as permy own self

>medicating idea----any ideas or opinions on this plan? Jan

>

> >>

>

>Jan

>If you have a doctor, why are you considering self medicating?

>This can be dangerous. If you feel the need to change or add

>an abx why not ask the doctor? Also, be sure to get regular

>blood work done to monitor your liver function... I have blood

>drawn every 4 weeks... My doctor tends to be cautious, and

>I appreciate that!

>Take care,

>Jane

>

>Many thanks to our founder and friend, Marta McCoy, for making

what it is today.

>

>

>Easy Reference:

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>

[Guest guest]

can anyone tell me the causes of a adnexal mass-urinarytract infection

and what one can do to heal.

[Guest guest]

Hi, I am not familiar with the term adnexal mass. But for a traditional urinary

tract infection involving e coli, D Mannose will kick it to the curb in short

order. Do a web search. for more info.

My mom had chronic uti's until she got on d mannose. Now she avoids anti

biotics and has no problems.

Blessings.

Donna

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

can anyone tell me the causes of a adnexal mass-urinarytract infection

and what one can do to heal.

[Guest guest]

I didn't answer your question about canning the goats milk. I wouldn't.

The only way to successfully preserve milk without freezing is to dry it

somehow, usually by making some kind of very dry cheese. But that would not

help your soap-making endeavors. So I would freeze it. It won't hurt it at

all. Those floaties won't hurt the soap, in fact they will probably melt

during the process. HTH. Lana. www.lanascreations.biz

[Guest guest]

I have seen many recipes that call for powdered goat or cow milk. Maybe

this will help.

SD

Re: Digest Number 1441

> I didn't answer your question about canning the goats milk. I wouldn't.

> The only way to successfully preserve milk without freezing is to dry it

> somehow, usually by making some kind of very dry cheese. But that would

not

> help your soap-making endeavors. So I would freeze it. It won't hurt it

at

> all. Those floaties won't hurt the soap, in fact they will probably melt

> during the process. HTH. Lana. www.lanascreations.biz

>

>

>

>

>

[Guest guest]

Jona...not everyone on steroids will gain weight. As a child I was on steroids for many years consecutively and I was teeny tiny. I have seldom ever weighed over 100 pounds. let me see with my 1st pregnancy I weighed 117 the day I gave birth....LOL.. I still fight to gain weight. I was at the doc today and checked in at 102!! Though my steroids are only occassional I still remain small. My mother has spoke often of how when I was young my tiny body was overpowered by swollen knees! Doc Shikler is one of the best so feel confident with the treatment he is providing brianna! By the way I passed all tests today and doc says I can resume my normal routine..YIPEEEEE!!! See thre days and I cant wait!!LOl..Donna

[Guest guest]

Jona...I meant Doc Meir...geez we are getting lots of KY folks here..Oh the confusion in my poor brain! I must resume some normalcy soon..lol...Donna

[Guest guest]

DONNA!!!!!! Sending you big congratulatory hugs!

Eli and Riley 4 poly

[Guest guest]

Hey ette.....ya know it was obviously the ex who had the problem. And you are so right...YOU ARE GOOD FOR SOMETHING...about your kids...you are MOM, no matter what and just as I experience it with my boys I am mom and every time I hear my son say, Mom, you are nice or mom my friend thinks you are cool I light up like the brightest of all christmas trees. remember we are all allowed down days (all moms and all kids with JRA) but whats important is we snap out of it and sometimes that means coming to the list to these great folks!!!Have all the fun you can each day and enjoy every moment..so there may be stares and finger pointing. I just say darn... I must really be special to get all the attention...LOLL..Donna

[Guest guest]

Hi Donna, na don't go to Shikler, A dermatologist referred us to him once a long time ago but I just decided to stay with shriners in Lexington with Dr. Mier. But I almost took up his offer. I know they are very good in Louiseville. And gosh I wished I weighed 102! I am glad you are feeling better now and you passed all the test! Thats great! Hugs from Jona and na 2 poly

faces1999@... wrote: Jona...not everyone on steroids will gain weight. As a child I was on steroids for many years consecutively and I was teeny tiny. I have seldom ever weighed over 100 pounds. let me see with my 1st pregnancy I weighed 117 the day I gave birth....LOL.. I still fight to gain weight. I was at the doc today and checked in at 102!! Though my steroids are only occassional I still remain small. My mother has spoke often of how when I was young my tiny body was overpowered by swollen knees! Doc Shikler is one of the best so feel confident with the treatment he is providing brianna! By the way I passed all tests today and doc says I can resume my normal routine..YIPEEEEE!!! See thre days and I cant wait!!LOl..Donna

[Guest guest]

Woops I didn't see this message yet and I've done wrote from the last one. I have the same memory problems. Jona

faces1999@... wrote: Jona...I meant Doc Meir...geez we are getting lots of KY folks here..Oh the confusion in my poor brain! I must resume some normalcy soon..lol...Donna

[Guest guest]

-Hi Donna, well people must stare at you because your pretty. And I

don't never get asked out by no one: ( My current boyfriend is

really beginning to get on my nerves. We don't even sleep in the

same bed! We are sick of each other! A lot changed when we found out

about the Jra and me and him kind of grew farther apart but we

havn't grew apart from na. We have just gotten closer to her.

It's difficult to get sleep around here too because of Lindsey(my 11

month old) She has been crying every night for the past few months

but it's not like a pain cry.(I remember what a pain cry sounds

like, like nas when she was an infant) It's more like a spoiled

cry because she has really been spoiled! Everytime she cries me or

(thats my boyfriend) will pick her up! Isn't that weird that

my boyfriend has a name like and I have a name like Jona

(seems like we should trade names LOL!) I hate having a name like

this! Well anyway Donna, The people are staring at you (and

anyone else that gets stared at) because they think your pretty.

Thats what my friend use to tell me because I would get really mad

when someone would stare at me and I never got asked out! My friend

said " well Jona their staring cause they probably think your

pretty. " So I try to keep that in my head but It still makes me

mad. Lots of Love from Jona and na 2 poly

-- In @y..., faces1999@a... wrote:

> Hey ette.....ya know it was obviously the ex who had the

problem. And you

> are so right...YOU ARE GOOD FOR SOMETHING...about your kids...you

are MOM, no

> matter what and just as I experience it with my boys I am mom and

every time

> I hear my son say, Mom, you are nice or mom my friend thinks you

are cool I

> light up like the brightest of all christmas trees. remember we

are all

> allowed down days (all moms and all kids with JRA) but whats

important is we

> snap out of it and sometimes that means coming to the list to

these great

> folks!!!Have all the fun you can each day and enjoy every

moment..so there

> may be stares and finger pointing. I just say darn... I must

really be

> special to get all the attention...LOLL..Donna

[Guest guest]

Donna

That really made me smile. The part where you said about the finger pointing and the stares. I never thought of it that way. I am trying to turn my life around and it's not easy at this time with also having a flare coming on, but i plan to have a wonderful summer with my children and I am going to keep coming here to talk to my dear friends.

Did you adopt yours? I did and the funny part of it all was my obgyn said I should have my own and that i would feel wonderful because it takes the Arthritis away. But then I learned after I would get the high fevers and pain all over again. I was just wondering if you had your children did you feel great??? It was my ex who had the problem as to why we couldn't have children of our own but hey I feel the children that God gave me are even better. i love them so much. However, the 21 year old is driving me crazy. i have to keep a step ahead of this kid. I have to watch every friend and party. I mean it's a turmoil. However, he is a nice boy and very sensitive too and that is wonderful. I always tell my children only the good stuff about them so they can be always feeling good about them self.

Well have a great week end.

ette

<))><

-- Re: Digest Number 1441

Hey ette.....ya know it was obviously the ex who had the problem. And you are so right...YOU ARE GOOD FOR SOMETHING...about your kids...you are MOM, no matter what and just as I experience it with my boys I am mom and every time I hear my son say, Mom, you are nice or mom my friend thinks you are cool I light up like the brightest of all christmas trees. remember we are all allowed down days (all moms and all kids with JRA) but whats important is we snap out of it and sometimes that means coming to the list to these great folks!!!Have all the fun you can each day and enjoy every moment..so there may be stares and finger pointing. I just say darn... I must really be special to get all the attention...LOLL..Donna

[Guest guest]

Can anybody tell me what is this 'cleanse' are all about?

I have a friend who is terminally ill of cancer. He might need

this alternative medication.

Right now, all the doctors do is only radiation, which weaken

him more and more. (He had taken chemotherapy earlier.

But obviously with no promising results!)

Thanks,

Iwan

Re: Re: Moral support

>

> Good luck on the cleanse Karyn! You hang in there. My brother started

the

> 21 day cleanse and the CEA level of cancer in his cells went from over 30

to

> 3.4 (almost normal) after only five days. There are a lot of things to

take

> during the cleanse but it will be well worth it.

>

> Nina Komniey

>

> www.admaxmarketing.com

> Ph: 949-369-7014

> Fax:603-994-1746

> M-F 9-5 PST

>

>

>

[Guest guest]

> I took my MTX last night and today I had my teenage daughter

> snarl: " You have a low aura--you're just a blob--go back to bed where

> you belong! " Then I went to visit my mom who mocked me a couple of

> times for minor " brain fog " moments. I was surprised at the lack of

> compassion, but will not dwell on it.

That's so mean! I'm sorry you have to deal with that

I've dealt with my share of un-commpassionate people (including *my*

teenage daughter) since my diagnosis and it hurts. My mother in

law's the worst, she has decided that this whole thing simply

does not exist. Unfortunately, I'm so depressed about the whole

thing right now that I do end up dwelling on it

I hope that you're able to stay strong...

Take care,

[Guest guest]

Hi everyone- I just had to chime in here. Anyone who doesnt have RA cannot possibly fathom the challenges. They speak from a place of denial or ignorance. My girlfriend just doesnt want to know, or says, " drink tea bark!! " . Dont let it hurt you, simply pity people who dont understand. Our illness reminds healthy people of their own mortality and most times just cant get their head around it. I strongly urge anyone dealing with RA to get into support therapy and possibly family sessions. I also cant urge strongly enough the attendance in your local area of a support group run by the arthritis foundation. Family members need to go with you to be educated about the disease, medications and daily life. Remember that this is a parasitic disease and feeds off depression and sorrow and stress. Hugs, Deborah

On 3/23/06, <kyrik@...> wrote:

> I took my MTX last night and today I had my teenage daughter> snarl: " You have a low aura--you're just a blob--go back to bed where

> you belong! " Then I went to visit my mom who mocked me a couple of> times for minor " brain fog " moments. I was surprised at the lack of> compassion, but will not dwell on it.That's so mean! I'm sorry you have to deal with that

I've dealt with my share of un-commpassionate people (including *my*teenage daughter) since my diagnosis and it hurts. My mother inlaw's the worst, she has decided that this whole thing simplydoes not exist. Unfortunately, I'm so depressed about the whole

thing right now that I do end up dwelling on it :)I hope that you're able to stay strong...Take care,

[Guest guest]

There is a wonderful site for people with all types of chronic illnesses who

really get it and go through the same problems with family and friends:

http://www.butyoudontlooksick.com

Check it out and check out the message board. It is a great group of which I

am a member.

>

> > I took my MTX last night and today I had my teenage daughter

> > snarl: " You have a low aura--you're just a blob--go back to bed where

> > you belong! " Then I went to visit my mom who mocked me a couple of

> > times for minor " brain fog " moments. I was surprised at the lack of

> > compassion, but will not dwell on it.

>

> That's so mean! I'm sorry you have to deal with that

>

> I've dealt with my share of un-commpassionate people (including *my*

> teenage daughter) since my diagnosis and it hurts. My mother in

> law's the worst, she has decided that this whole thing simply

> does not exist. Unfortunately, I'm so depressed about the whole

> thing right now that I do end up dwelling on it

>

> I hope that you're able to stay strong...

>

> Take care,

>

>

>

[Guest guest]

Anybody used any Lakhovsky coils on any plants? Some pretty impressive

photos on the web about these used on the greenery. pj

[Guest guest]

Hi ,

I am training a 30y old student that have almost the same problem. Looking

at the EEG I am able to see if he " begans to think " . he is very intelligent

but could not do one Semester of university-studies.

Is is now much better: he is able to train and to stay for 10 min, without

exessive thetas. and he realizes that. For training we did all the time 1C,

SMRup, theta down at Cz, or Fz or FCz.

He thinks and speakes in imageries so a lot, that he was diagnosed - after a

short period of anxiety having some tropical diseases,after a tropical

journey and malaria, - to have schizophrenia.

best cornelia dollfus, MD

> --- Ursprüngliche Nachricht ---

> Von:

> An:

> Betreff: Digest Number 1441

> Datum: 8 Apr 2006 13:14:21 -0000

>

> There is 1 message in this issue.

>

> Topics in this digest:

>

> 1. FW: Theta goes up when she talks

> From: " Key " danielkey@...

>

> ________________________________________________________________________

> ________________________________________________________________________

>

> Message 1

> From: " Key " danielkey@...

> Date: Fri Apr 7, 2006 2:21pm(PDT)

> Subject: FW: Theta goes up when she talks

>

> Hey everyone.

>

> Working with a young woman who's decided for the second time to try for

> her

> PhD. She had some accomodations in undergraduate, but because of anxiety,

> and perfectionism was always late making paper deadlines, etc. I did a

> TLC

> assessment on her and found that at least in the frontal lobes at least

> 70+%

> of the spectrum was low frequency waves. Everywhere else they were

> usually

> over 50%. That in itself is enough to make a good case for severe ADD (I

> think). The " testers " using Conners and the standard battery of

> performance

> tests, IQ, etc. have downplayed her ADD, and mostly " blamed " her inability

> to perform in academics on her depression (which came first the chicken or

> the egg ie depression, or ADD).

>

> The other day I was using a depression protocol which concentrates on the

> L

> frontal and pre-frontal cortex, and noticed something which may or may not

> have significance. The site was left frontal, and it was 2C. Every time

> she would talk, theta would increase. So I thought, on task she reverse

> activated anyway, wonder what would happen if she read something. When

> she

> read outloud, nothing happened. She read several pages of fairly

> difficult

> material, and the graph never moved, but the instant she had to think

> about

> what she was talking about, everything including theta went up. I asked

> her

> if she thought in images or sentences, and she said mostly images I guess.

>

> Is this something people have found to be fairly universal, that thinking

> elevates low frequency, or could it be true of individuals with ADD, or is

> thinking in images significant ?

>

> Thanks for any thoughts

>

>

>

>

>

> ________________________________________________________________________

> ________________________________________________________________________

>

>

>

> ------------------------------------------------------------------------

>