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Dear Amy, (Melinda, Kathy and Louis)

Thanks so much for your welcome and replies. I am scared, and this means a

huge amount to me.

I will order Tamar's book. (Couldn't see the others on Amazon). I will look

at the UK site. I hope to see someone from the UK posting one day!! Things

are certainly different over here...guess it's to do with our run down

National Health Service. Definitely too few psychologists- the ones there

are all educational....

Ami is refusing to admit there is a problem, and certainly won't accept

meds, so I'm letting her know that meds are out there and then I'll have to

wait. Lack of acceptance may also make ERP difficult, but I'll se when I've

read the book.

Meanwhile she has taken 5 mg inositol AGAIN tonight :o)) (so long as I take

one too!), as a combined B vit. When I'm near a health store I'll try to

find it on its own, as the other B vits may be too high a dose for her size.

Meanwhile at least it feels like I'm doing SOMETHING........

Any words of encouragement, idea of dose etc for an 11 year old trying

inositol alone?

Thanks again...so much

Alice

Re: inositol

>Hi,

>I have introduced myself as a new member, with an 11 year old, ocd

daughter,

>Ami. It seems that the only help I MAY get from our UK medical profession

>is medication, as the psychiatric and psychology services are not good

>here-for this and many other conditions. However my daughter flatly

refuses

>to believe she has a problem. Refuses to believe that her compulsions are

>debilitating in any way, and obviously refuses to take any medication. I

>did manage to persuade her to take a multi B-vit last night with 5mg

>inositol in it. This took half an hour and she said she'd only do it once.

>Then I found, that having brought the whole subject up with her, her

nightly

>rituals with me observing, took twice as long. I often feel it's worse

when

>I'm around. Why is this? Is this a control thing? Somehow it makes the

>whole thing look like more of an act to me. However I have heard her

>rearranging curtains and opening and closing drawers when I'm not around to

>see it. Its very confusing.

>On the med thing...do I just gently suggest that there are meds there for

>when she's ready and leave it at that?

>Alice

>

>

>You may subscribe to the OCD-L by emailing listserv@... . In

the body of your message write: subscribe OCD-L your name. You may

subscribe to the Parents of Adults with OCD List at

parentsofadultswithOCD-subscribe . You may subscribe to

the OCD and Homeschooling List at

ocdandhomeschooling-subscribe . You may change your

subscription format or access the files, bookmarks, and archives for our

list at . Our list advisors

are Tamar Chansky, Ph.D., Aureen Pinto Wagner, Ph.D., and Dan Geller, M.D.

Our list moderators are Birkhan, Kathy Hammes, Jule Monnens, Gail

Pesses, Kathy , and Jackie Stout. Subscription issues or

suggestions may be addressed to Louis Harkins, list owner, at

lharkins@... .

>

>

>

>

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Guest guest

Sorry, Alice, I don't know any thing about inositol. However, since

also refuses prescription meds, I will investigate it. He

has no aversion to taking vitamins and currently takes a multi-

vitamin with minerals and fish oil capsules (to increase body fat).

Thanks for bringing to light yet another option.

Melinda s.

Dallas

> Dear Amy, (Melinda, Kathy and Louis)

> Thanks so much for your welcome and replies. I am scared, and this

means a

> huge amount to me.

> I will order Tamar's book. (Couldn't see the others on Amazon). I

will look

> at the UK site. I hope to see someone from the UK posting one

day!! Things

> are certainly different over here...guess it's to do with our run

down

> National Health Service. Definitely too few psychologists- the

ones there

> are all educational....

> Ami is refusing to admit there is a problem, and certainly won't

accept

> meds, so I'm letting her know that meds are out there and then I'll

have to

> wait. Lack of acceptance may also make ERP difficult, but I'll se

when I've

> read the book.

> Meanwhile she has taken 5 mg inositol AGAIN tonight :o)) (so long

as I take

> one too!), as a combined B vit. When I'm near a health store I'll

try to

> find it on its own, as the other B vits may be too high a dose for

her size.

> Meanwhile at least it feels like I'm doing SOMETHING........

>

> Any words of encouragement, idea of dose etc for an 11 year old

trying

> inositol alone?

> Thanks again...so much

> Alice

>

>

>

>

>

> Re: inositol

>

>

> >Hi,

> >I have introduced myself as a new member, with an 11 year old, ocd

> daughter,

> >Ami. It seems that the only help I MAY get from our UK medical

profession

> >is medication, as the psychiatric and psychology services are not

good

> >here-for this and many other conditions. However my daughter

flatly

> refuses

> >to believe she has a problem. Refuses to believe that her

compulsions are

> >debilitating in any way, and obviously refuses to take any

medication. I

> >did manage to persuade her to take a multi B-vit last night with

5mg

> >inositol in it. This took half an hour and she said she'd only do

it once.

> >Then I found, that having brought the whole subject up with her,

her

> nightly

> >rituals with me observing, took twice as long. I often feel it's

worse

> when

> >I'm around. Why is this? Is this a control thing? Somehow it

makes the

> >whole thing look like more of an act to me. However I have heard

her

> >rearranging curtains and opening and closing drawers when I'm not

around to

> >see it. Its very confusing.

> >On the med thing...do I just gently suggest that there are meds

there for

> >when she's ready and leave it at that?

> >Alice

> >

> >

> >You may subscribe to the OCD-L by emailing listserv@v... . In

> the body of your message write: subscribe OCD-L your name. You

may

> subscribe to the Parents of Adults with OCD List at

> parentsofadultswithOCD-subscribe@y... . You may subscribe to

> the OCD and Homeschooling List at

> ocdandhomeschooling-subscribe@y... . You may change your

> subscription format or access the files, bookmarks, and archives

for our

> list at . Our list

advisors

> are Tamar Chansky, Ph.D., Aureen Pinto Wagner, Ph.D., and Dan

Geller, M.D.

> Our list moderators are Birkhan, Kathy Hammes, Jule Monnens,

Gail

> Pesses, Kathy , and Jackie Stout. Subscription issues or

> suggestions may be addressed to Louis Harkins, list owner, at

> lharkins@b... .

> >

> >

> >

> >

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  • 4 months later...

Thanks all for the birthday well wishes. Just realized

one " up " side to turning 50. I am now eligible to join

AARP!!! Terri

=====

searching for Deborah

dob 1/14/57 in nna, Fl

Relinquished in Chicago, 1961

brother and 5 other siblings searching

Half-sib found 1-16-00!

__________________________________________________

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  • 2 months later...

> Mike is doing better. He gets out of the hospital today. They will keep

> him on the beta blocker but there is no restrictions on him. It was his

Glad to hear this crisis is over. Hopefully the new med will keep him

stable.

Sue in NJ

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  • 3 weeks later...

I am so very truly happy to hear that. Our families thoughts and prayers are

with you. Take care and we are rooting for you.

Thank You

> Hi Everyone,

> Thank you for all your letters they meant so much to me. I love all of my

groups! It is so great to have the type of support that you guys give. Thank

You all once again. Well we went to have the procedure done yesterday.

First they hooked Mike up to a table to flip him around on and see if that

effected his heart.... Nothing, then they inserted the tubes for the EP

Study. to see if they stimulated his heart would there be any fluttering,

when the entered into the heart without stimulating it there was fluttering,

it started by itself and stopped on it's own to. However when the dr was

stimulating it there was no flutter. So in other words Mike has a healthy

heart.. Everyone's heart has fluttering in it every now and then. So in the

mean time they want him to still wear the heart monitor and stay off his

pills. But they are now looking at the fact that it could be epilepsy

without seizure activity in the brain when they do test. So we still have

nothing concrete. But the good news is that with several phone calls on

Monday, we finally got an answer from the insurance company Mike was

accepted, and they will cover everything from 1/1/02 and on. THANK GOD!!! So

today after what feels like forever not keeping track of what I've been

eating, I started again ! It feels so good to be in control of what I'm

eating. I know that I've strayed, because of stress. But I've tried to be a

ware of my eating.

> Thank everyone...

>

>

>

>

>

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I'm glad to hear that everything went well, and doubly happy to hear

about the insurance. My mom went round and round with insurance both

this year and last as she's self-insured (The premiums boggle the

mind!) I'm also very glad that they're back-dating it to last month.

What a boon!

Congratulations on getting back on track.

K.

303/294/140-150

> Hi Everyone,

> Thank you for all your letters they meant so much to me. I love all of my

groups! It is so great to have the type of support that you guys give. Thank You

all once again.

> Thank everyone...

>

>

>

>

>

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  • 3 weeks later...
Guest guest

In a message dated 3/7/02 3:14:26 AM Central Standard Time, svaux@...

writes:

> Thanks Cat for all your info you are so willing to share. You've been a big

> help for a lot of us. =^..^= Sandy

>

>

I second and third that!

¸..·´¨¨)) -:¦:-

¸.·´ .·´¨¨))

((¸¸.·´ ..·´ -:¦:- Sage -:¦:-

-:¦:- ((¸¸.·´*

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  • 4 weeks later...
Guest guest

Hi Shellely,

I can totally relate to how you're feeling. Hunter is seven, and every

time it is time for his IV, he kicks and screams, not understanding why we are

holding him down and torturing him. I usually end up crying all afternoon when

we get home and asking God why this is happening to my precious son. I too feel

like what have I done wrong. We still don't know if this is genetic, I have my

doubts. This whole situation is like a continuous nightmare for me. I know

things could be worse, but it is hard not to feel jealous of people with healthy

kids. I know this is where most of my depression comes from.

On the otherhand, I am trying to praise God everyday for the air that we

breath, and for the life he has given us. None of us knows when it will be our

last day on earth. Because of this, I have developed a greater relationship

with God. I try not to take anything for granted.

Telling your son I'm sure will be difficult. Kids are very tough and can

handle a lot. Everytime Hunter goes in for his IV, we have a talk about the

immune system, and if he didn't get this IVIG, he would be very sick like he was

in the past. They can only understand so much, so it is hard. We just try and

make everything as comfortable as possible. We numb with the Emla cream, and

the nurse usually injects Lidocaine to numb it more. I try to hydrate him well

before we go in. That usually helps. We draw blood each time for an IGG level.

I insist that we draw it off of the IV site, not poke his arm again. Each stick

is precious. Then between IV's, I try and forget about his illness as much as I

can and try and lead a normal life. From the past e-mail, I think you said he

has to go in every 3 weeks. Hunter started out that way also, I insisted we

check levels and try spreading them out. Hunter has been very healthy except

for a few illnesses inbetween. He is full of energy. They let it up to me when

we want to go in. We have been going in every 5-6, (last time 7) weeks.

Granted the 7 is to long and his levels are lower, but I have been experimenting

with how long we can go. If I wouldn't have spoke up, we'd still be doing it

every 3 weeks-which is torture for Hunter.

Sorry so long, but keep in touch with all of us and it is ok to vent and

feel the way you do.

God Bless,

Temme-mom to Dylan-9 and Hunter-7 (agammaglobulinemia)

thank you

Hello group,

I just wanted to say thank you for your e-mails. They really mean a lot to me.

It just doesn't seem fair that God would allow these things to happen to

children who didn't do anything to deserve a life sentence of IVIG and chronic

infections. My heart aches for and what he'll have to go through for a

long time. I will say though, that has two things going for him that

will make him be able to handle this much better than I am: he has terrific

veins and he has a temperament that will allow him to " go with the punches. "

Perhaps you can help me with; when and how should I tell ? Although he

is an even tempered little boy, I am afraid if I tell him in the wrong way, he

will keep his feelings to himself and cause even more damage. How does a mom

tell her eight year old little boy that he will probably have this disease

forever?

I can't stop crying. I am so hurt by what the doctor said.

(; CVID/ IGG deficiency, asthma; Hope; cystinuria)

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  • 1 month later...
Guest guest

Hello

I had started a few, even bought leather bound blank books for doing so

but I always forgot to pack the journal. I have a few odd photos but

most pictures went undeveloped. I guess I never really put much

emphasis on chronically my journeys, I always thought I would return

with somebody to share the sights, it's difficult to enjoy anything when

on a business trip by yourself and if you're with co-workers, you either

don't make it out of the bar or the fast food places.

Regards,

daystar1210 wrote:

> Thank you for sharing your story... I admire your strength and

> courage...

>

> Thank you for telling me about your adventure. It did not sound at

> all

> glamorous but very trialsome for you. I am so glad that you make

> it back home...safely.

>

> , did you ever keep a journal about your travels? Did you

> take pictures?... Just wondering.

>

> Looking forward to talking to you again,

> Take care of yourself,

>

>

>

>

>

....

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  • 1 month later...
  • 4 weeks later...
  • 4 weeks later...
  • 1 month later...

Hello Melody, Could you give me more info about the ratio of water to PS20?

Do you mean we don't have to use alcohol? Thanks, Jacque

Hello again Melody, thank you very much. I have a GD to make gifts for by

Sept 3, and will be able to include that.

>

>

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  • 3 weeks later...

It's fun to see others as excited about this as I am. I had a blast

filtering the beeswax and then doing blossoms of roses today so I know how

much fun you're having Candy. :) I'm impatiently waiting on orders myself.

Like a kid at Christmas aren't we?

Pam

I got my firstbatch of foaming bottles today !!! I am so excited!!!! Now I

have to figure out what recipe to put in them. Any and all recipes are

great. Thanks again. Can you tell I am just learning? HA,Ha,Ha.

Candy

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It's fun to see others as excited about this as I am. I had a blast

filtering the beeswax and then doing blossoms of roses today so I know how

much fun you're having Candy. :) I'm impatiently waiting on orders myself.

Like a kid at Christmas aren't we?

Pam

I got my firstbatch of foaming bottles today !!! I am so excited!!!! Now I

have to figure out what recipe to put in them. Any and all recipes are

great. Thanks again. Can you tell I am just learning? HA,Ha,Ha.

Candy

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  • 2 weeks later...

Dear Dan, & Caroline,

thank you! Dan, I did start my folic acid late, so perhaps this is definitely a

problem, although, on it...I have been having this problem lately, but no so bad

as this time. , thank you friend also...your kindness is much

appreciated. Caroline as always..thank you also and if possible I will talk to

my rheumy tomorrow. It was his last day in my area today, although he wasn't at

the office. He starts tomorrow at the UCONN University Hospital. He was once

there before, but literally has to start all over again. I am hoping to be able

to find him and talk to him..and yes...there are actual sores on my right arm. I

never thought of these before. I didn't think it was anything at all.

Anyway..thank you very much, ALL of you for the love and support as always.

Dan..I added you to my addy list..!

Love, sue #2

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I was wondering if anyone here has tried EFT or NAET for their children's

behaviors? We have just started the NAET because frankly, the gfcf diet did

not work out for us. I tried it for almost a year but I just knew that Evan

is allergic or intolerant to more than gluten and casein but I was never

able to go deeper into eliminating more food. We are just into the

treatments so we cannot be positive what benifits we will be seeing but I

have friends who have seen great benifits. My 31 yo daughter has been

suffering with depression with her bipolar and after doing the first brain

body balance treatment she has been full of unusal energy and much less

depressed. EFT uses similar methods but is not for allergy elimination but

Emotional Freedom. I am trying to learn more about it because it also is

suppose to have helpd some with autism.

Betty

grandma and guardian to

- 11 yo-- Bipolar/ADHD on Depakote, Adderall

Evan - 8 yo nonverbal autism on 3 mg Risperdal

- 6 - Bipolar/ADHD/RAD/PTSD on Depakote, Adderall

mother to , their mom - Bipolar/ADHD on Topamax

wife to Bob too many meds to remember

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

From: " eashtonb " <eashtonb@...>

> The doctor prescribed Risperdal too.. We havent given it to

> him, we didnt think he was that bad. Not that he isnt bad.... LOL

> just that he has been worse... had he continued on that path I would

> be medicated right along side of him... He is still very violent

> toward me and his sisters... He hasnt hit anyone at school in a

> while, but threatened to hit a student the other day when I was

> spying at his mothers day out... He was walking behind another boy

> holding a huge truck up menacingly... as if he were about to hit the

> child with it... The boy was not running but walking very fast trying

> to get away and was just grinning, walking faster too... So I

> am pretty sure he is worse there than they let on...

>

> He did try to hit the aid at his special ed preschool, and we were

> told he would be kicked out if he hit another child, during our first

> IEP meeting... and he is only 3. So I know here they threaten that

> they do it..( kick them out that is) ...

>

> And I have heard that if he is removed from his class, they cant

> just kick him out and thats it... they have to provide/pay for an

> alternative placement... either private school, in-home etc...

>

>

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Hello Group, I am a LPC/School Psychologist in private practice in

Tulsa, OK and have successfully used EFT for autism, ADHD/ADD and

behavioral issues. It has proven very effective when learned and

used properly. You can go to www.emofree.com for a list of trained

providers in your area. I highly recommend trying alternative

methods to assist our kids in leading happier, more productive

lives. With EFT there are no drugs, nothing invasive and it is quick

and effective. If you would like further info the above website is a

wealth of information, too.

Hope this helps,

Debbie

> I was wondering if anyone here has tried EFT or NAET for their

children's

> behaviors? We have just started the NAET because frankly, the gfcf

diet did

> not work out for us. I tried it for almost a year but I just knew

that Evan

> is allergic or intolerant to more than gluten and casein but I was

never

> able to go deeper into eliminating more food. We are just into the

> treatments so we cannot be positive what benifits we will be seeing

but I

> have friends who have seen great benifits. My 31 yo daughter has

been

> suffering with depression with her bipolar and after doing the

first brain

> body balance treatment she has been full of unusal energy and much

less

> depressed. EFT uses similar methods but is not for allergy

elimination but

> Emotional Freedom. I am trying to learn more about it because it

also is

> suppose to have helpd some with autism.

>

>

> Betty

> grandma and guardian to

> - 11 yo-- Bipolar/ADHD on Depakote, Adderall

> Evan - 8 yo nonverbal autism on 3 mg Risperdal

> - 6 - Bipolar/ADHD/RAD/PTSD on Depakote, Adderall

> mother to , their mom - Bipolar/ADHD on Topamax

> wife to Bob too many meds to remember

> ----- Original Message -----

> From: " eashtonb " <eashtonb@a...>

>

>

> > The doctor prescribed Risperdal too.. We havent given it to

> > him, we didnt think he was that bad. Not that he isnt bad.... LOL

> > just that he has been worse... had he continued on that path I

would

> > be medicated right along side of him... He is still very violent

> > toward me and his sisters... He hasnt hit anyone at school in a

> > while, but threatened to hit a student the other day when I was

> > spying at his mothers day out... He was walking behind another boy

> > holding a huge truck up menacingly... as if he were about to hit

the

> > child with it... The boy was not running but walking very fast

trying

> > to get away and was just grinning, walking faster too...

So I

> > am pretty sure he is worse there than they let on...

> >

> > He did try to hit the aid at his special ed preschool, and we

were

> > told he would be kicked out if he hit another child, during our

first

> > IEP meeting... and he is only 3. So I know here they threaten that

> > they do it..( kick them out that is) ...

> >

> > And I have heard that if he is removed from his class, they cant

> > just kick him out and thats it... they have to provide/pay for an

> > alternative placement... either private school, in-home etc...

> >

> >

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Thank you, Debbie.

Betty

grandma and guardian to

- 11 yo-- Bipolar/ADHD on Depakote, Adderall

Evan - 8 yo nonverbal autism on 3 mg Risperdal

- 6 - Bipolar/ADHD/RAD/PTSD on Depakote, Adderall

mother to , their mom - Bipolar/ADHD on Topamax

wife to Bob too many meds to remember

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

From: " Debbie " <hypnosis8@...>

> Hello Group, I am a LPC/School Psychologist in private practice in

> Tulsa, OK and have successfully used EFT for autism, ADHD/ADD and

> behavioral issues. It has proven very effective when learned and

> used properly. You can go to www.emofree.com for a list of trained

> providers in your area. I highly recommend trying alternative

> methods to assist our kids in leading happier, more productive

> lives. With EFT there are no drugs, nothing invasive and it is quick

> and effective. If you would like further info the above website is a

> wealth of information, too.

> Hope this helps,

> Debbie

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EFT stands for Emotional Freedom Therapy.

Betty

grandma and guardian to

- 11 yo-- Bipolar/ADHD on Depakote, Adderall

Evan - 8 yo nonverbal autism on 3 mg Risperdal

- 6 - Bipolar/ADHD/RAD/PTSD on Depakote, Adderall

mother to , their mom - Bipolar/ADHD on Topamax

wife to Bob too many meds to remember

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

From: " claire neville " <daisygoogles@...>

>

> Hi,

> What does EFT stand for?

> and what does LPC? /School Psych the LPC part mean??

>

> Thank you,

>

> mom of Jack age 8 adhd ld asthmatic

> peter age 6 autistic adhd ld etc

> wife of Bill NYCP Sargeant

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  • 3 weeks later...

LOL,,I should re-post the conversation I had with myself one night

when I went over to mcDs intending to cheat and get chocolate chip

cookies (homemade ones NOT those little hard things).

It was so funny (in retrospect). It was SO one of those " devil on

one shoulder, angel on the other " moments.

Okay so here I am walking across the street to mcD's for cookies. (I

used to live about 30 steps from Mic's front door,,arrggghh, luckily

the only thing they have that I like are the shakes, ice cream and

those cookies,,,mmmmmmmmmmmm warm and melty,,,ACK,,slaps

face,,,anyway).

Angel: Just WHAT do you think you're doing????!!!!!

Devil: MIND your own business, I just cleaned house for 4 hours,,,I'm

tired, cranky, cold and I WANT a REWARD!!!!

Angel: mutter, mutter, mutter,,BAD,,BAD girl,,,,

I reach the door,,,I go in,,I ask for 6 CC Cookies.

Counter boy: I'm sorry ma'am we're out right now

Angel: HAH!!! Serves you right,,,SEE? It's NOT meant to be.

Devil: WE'LL see about that!!!!

Me (to counter boy): How long before you have a batch ready??

Counter boy: 8-12 minutes.

Me: okay thank you.

So, I walk out into the Chevron quik mart part of the store.

To wait.

(mwah haha).

Angel: LOOK, this is a SIGN that you are not SUPPOSED to cheat.

Devil: YOU just shut up before I knock your lily white pansy little

winged a$$ on this floor, I am GETTING cookies, I DESERVE cookies!!!

Angel: ALLRIGHT,,,THAT does it,,,,You get your FAT behind HOME and go

to bed,,,you need REST you moron, NOT cookies!!! NOW MARCH!!!!!!!!!!

LET'S go,,,,,you're gonna take a hot bath and go to bed,,,now quit

your sniveling,,,get your fat rear end HOME!!!!

Man!!! Those angels can be so MEAN!!!!!

LOL,,,

(by the way,,the angel DID win. I didn't get cookies).

The moral of the story is that you don't want to have a devil and

angel duking it out on your shoulders in public, it's embarrassing.

heehee,,,,but really,,,,sometimes you just GOTTA " yell " at yourself.

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> > LOL,,,

> (by the way,,the angel DID win. I didn't get cookies).

>

> The moral of the story is that you don't want to have a devil and

> angel duking it out on your shoulders in public, it's

embarrassing.

> heehee,,,,but really,,,,sometimes you just GOTTA " yell " at yourself.

Reminds me of the time I took the milk duds off the shelf, put them

back on the shelf, took them off, put them back on...anyone near me

must have thought I was crazy!

Colleen

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ROFLMAO!!!!!!! I just printed that to show to my friend. I was

whining to him today about the candy bowl being within reach at work,

he told me that for every piece of candy that I ate I had to do 5

push ups.......maybe I will just tell him that you will send your

little " Guido Angel " after me :)

B.J. :)

-- In @y..., canvasshoes2 <no_reply@y...> wrote:

> LOL,,I should re-post the conversation I had with myself one night

> when I went over to mcDs intending to cheat and get chocolate chip

> cookies (homemade ones NOT those little hard things).

>

> It was so funny (in retrospect). It was SO one of those " devil on

> one shoulder, angel on the other " moments.

>

> Okay so here I am walking across the street to mcD's for cookies.

(I

> used to live about 30 steps from Mic's front door,,arrggghh,

luckily

> the only thing they have that I like are the shakes, ice cream and

> those cookies,,,mmmmmmmmmmmm warm and melty,,,ACK,,slaps

> face,,,anyway).

>

> Angel: Just WHAT do you think you're doing????!!!!!

>

> Devil: MIND your own business, I just cleaned house for 4

hours,,,I'm

> tired, cranky, cold and I WANT a REWARD!!!!

>

> Angel: mutter, mutter, mutter,,BAD,,BAD girl,,,,

>

> I reach the door,,,I go in,,I ask for 6 CC Cookies.

>

> Counter boy: I'm sorry ma'am we're out right now

>

> Angel: HAH!!! Serves you right,,,SEE? It's NOT meant to be.

>

> Devil: WE'LL see about that!!!!

>

> Me (to counter boy): How long before you have a batch ready??

>

> Counter boy: 8-12 minutes.

>

> Me: okay thank you.

>

> So, I walk out into the Chevron quik mart part of the store.

>

> To wait.

>

> (mwah haha).

>

> Angel: LOOK, this is a SIGN that you are not SUPPOSED to cheat.

>

> Devil: YOU just shut up before I knock your lily white pansy little

> winged a$$ on this floor, I am GETTING cookies, I DESERVE cookies!!!

>

> Angel: ALLRIGHT,,,THAT does it,,,,You get your FAT behind HOME and

go

> to bed,,,you need REST you moron, NOT cookies!!! NOW

MARCH!!!!!!!!!!

>

> LET'S go,,,,,you're gonna take a hot bath and go to bed,,,now quit

> your sniveling,,,get your fat rear end HOME!!!!

>

> Man!!! Those angels can be so MEAN!!!!!

>

> LOL,,,

> (by the way,,the angel DID win. I didn't get cookies).

>

> The moral of the story is that you don't want to have a devil and

> angel duking it out on your shoulders in public, it's

embarrassing.

> heehee,,,,but really,,,,sometimes you just GOTTA " yell " at yourself.

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hahahaha! I'm laughing so hard at this visual!

> LOL,,I should re-post the conversation I had with myself one night

> when I went over to mcDs intending to cheat and get chocolate chip

> cookies (homemade ones NOT those little hard things).

>

> It was so funny (in retrospect). It was SO one of those " devil on

> one shoulder, angel on the other " moments.

>

> Okay so here I am walking across the street to mcD's for cookies.

(I

> used to live about 30 steps from Mic's front door,,arrggghh,

luckily

> the only thing they have that I like are the shakes, ice cream and

> those cookies,,,mmmmmmmmmmmm warm and melty,,,ACK,,slaps

> face,,,anyway).

>

> Angel: Just WHAT do you think you're doing????!!!!!

>

> Devil: MIND your own business, I just cleaned house for 4

hours,,,I'm

> tired, cranky, cold and I WANT a REWARD!!!!

>

> Angel: mutter, mutter, mutter,,BAD,,BAD girl,,,,

>

> I reach the door,,,I go in,,I ask for 6 CC Cookies.

>

> Counter boy: I'm sorry ma'am we're out right now

>

> Angel: HAH!!! Serves you right,,,SEE? It's NOT meant to be.

>

> Devil: WE'LL see about that!!!!

>

> Me (to counter boy): How long before you have a batch ready??

>

> Counter boy: 8-12 minutes.

>

> Me: okay thank you.

>

> So, I walk out into the Chevron quik mart part of the store.

>

> To wait.

>

> (mwah haha).

>

> Angel: LOOK, this is a SIGN that you are not SUPPOSED to cheat.

>

> Devil: YOU just shut up before I knock your lily white pansy little

> winged a$$ on this floor, I am GETTING cookies, I DESERVE cookies!!!

>

> Angel: ALLRIGHT,,,THAT does it,,,,You get your FAT behind HOME and

go

> to bed,,,you need REST you moron, NOT cookies!!! NOW

MARCH!!!!!!!!!!

>

> LET'S go,,,,,you're gonna take a hot bath and go to bed,,,now quit

> your sniveling,,,get your fat rear end HOME!!!!

>

> Man!!! Those angels can be so MEAN!!!!!

>

> LOL,,,

> (by the way,,the angel DID win. I didn't get cookies).

>

> The moral of the story is that you don't want to have a devil and

> angel duking it out on your shoulders in public, it's

embarrassing.

> heehee,,,,but really,,,,sometimes you just GOTTA " yell " at yourself.

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