Re: Becky's site, parents, my support group

[Guest guest]

Hi everyone

Dimitrios here

what is the << Becky ur site>>

Thanks alot

Dimitrios

Alisha Peckham wrote:

>

>

> alisha here,

> first of all i have to say that Becky ur site was great. i just loved it so

> much and i am going to add it to my webpage of links. to the subject of

> parents, i am the only female affected in my whole family (or at least i am

> pretty sure), this disorder is a family secret and i am being talked about

> by my family, my progress, and what i shouldn't be doing. this is just

> something u don't talk about and i really the only one doing just that. i

> have no family support at all, i am dealing with this all by myself and i

> can't keep doing it all by myself. it is so stressful and i should have

> support but i am not getting any. i am being blamed for not talking to my

> parents but i don't want to at all, they don't understand what i am going

> through and they feel that they do. i feel so rejected and ostracized from

> my family. they r making it so hard on me. when my parents talk to me they

> yell and scream at me for everything, they want to know the answers to

> anything that they ask and if i don't know, say that i don't know, i don't

> remember, what r u talking about? they get angry if i say those sentences.

> they really don't talk to me, they have to be told by my psychologist!!!!

> they get angry when i don't talk to them. besides CMT i have depression,

> memory loss and loss of concentration. i hate it so much, i have such bad

> marks in school and i am getting harassed by my teachers again for

> explanations. i have so much inside me and the only support i get is from

> the groups i belong to and my best friends. my parents feel that i am

> obsessed with CMT but i am not, its what has taken hold of my life. when i

> graduate from high school i will be going to university and become a genetic

> counsellor. i will do this and i have been told that i will be crushing my

> dreams and that i am crushing them. i don't know what to do at all.

> on a lighter note, i have a support group for kids and teenagers with CMT,

> if u have a child with CMT please ask them to join, i created the list and i

> am a teenager. i want to understand and support them, i

> want to be able to help. please ask them to join.

>

> sorry its so long, i just had a lot to say.

>

> " I am not crazy, I am just a teenager! "

> http://home.talkcity.com/OceanBlvd/cmtx/index.html

> ICQ # 47695812

> for information on CMT go here

> www.cmtint.org/

> are u a kid or teenager with CMT???

> wanna talk to others with CMT????

> join here if u want to

> CMTchildren-subscribe (AT) onelist (DOT) com

>

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