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Re: Angry at OCD!!!

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Thank you so much ! This website is really my only support group right

now. I knew someone would understand. You described it perfectly! I do feel

like I'm a barometer, and everything indicates a tornado headed right straight

into his/our lives. It is heartbreaking to watch! As a parent, I want to be

able to do so much more. I want to take it from him before it actually hits.

I feel so helpless at times.

Corinna in TX

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Thanks Kathy! I'm glad I have this support and understanding. You are right

about family. I was just discussing yesterday with my mother some concerns

about Garrett's behavior and symptoms. She tried to write most of it off to

normal preadolescent behavior. She just doesn't get his shear panic and anxiety

over these things. She doesn't understand that these worries and thoughts

reak havic in his life. They are not just " normal " childhood concerns.

Anyway, they did do the quick strep test in the office, but they always send

the test out for the more advanced test also. I'm also waiting for results

from his blood work. His pediatrician is checking his strep antibiodies levels.

I am beginning to wonder if the strep could be somewhere else at times. I

plan to request antibiodics no matter what the blood work reveals.

Also, I have kept him on Claritin also, thinking it might help prevent this

summer episode he typically gets. I guess in his case it didn't.

Thanks again.

Corinna in TX

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

> Also, I have kept him on Claritin also, thinking it might help prevent

this

> summer episode he typically gets. I guess in his case it didn't.

Corinna I have never been *sure* this is working for us. My daughter didn't

have her usual big upswing in OCD symptoms from early spring thru early

summer these past two seasons. That coincided with my being aggressive with

the allergy med. I don't have any way of knowing whether it made a

difference OCD-wise or not...perhaps she would not have tanked these past

two springs anyway.

Good luck,

Kathy R. in Indiana

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<<Try not to discuss or expect support from those who do not " get " OCD.

I

found so many tried to comfort me by suggesting I was overreacting or

worrying over normal kid behavior. But the effect on me was anything but

comforting, I felt very alone.>>

**There is a wonderful video tape that we got from the OC Foundation. It

is called " The Touching Tree " . We have had a lot of success passing it

around to friends to watch. I do not think that anyone who does not have

OCD or live with someone who has it will " get " OCD. But this video has

been a wonderful tool for helping our friends understand where our dd is

coming from. Many of the friends in our congregation actually said that

they cried when they watched it because they had no idea how painful this

must be for Meghan until they saw it. The video is nice also because I

think more people are apt to watch it than read a whole book about OCD

and I think that it really hits on a lot of important points like the

fact that they may not " see " OCD because it can be so secretive. I know

that every family has a different way of doing things, but we chose to do

it this way because our friends are just like family to us and we wanted

to make sure our daughter was not misunderstood in any way and that we

had the support and understanding we needed also. Just a suggestion.

**

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Thanks for the video suggestion. I will try to find it. I would atleast

like grandparents and some other family members to watch it. It would help if

they had atleast a small understanding of OCD.

Corinna in TX

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