RE: Re: Response to !

[Guest guest]

: I have had many hurtful and rude comments made to me as well, not

just by but others. I have found if I am going to remain on the board,

which I am, I have to have a tough skin and let the ignorance roll off my back.

No one sees what you go through on a daily basis. No one knows the heartache

or pain you feel and no one really will ever be able to over the computer.

Just hang tough, choose to read the e mails that you are interested in and

keep posting what you are feeling. I am sure had some tough days too, and

although she comes across as rude sometimes,it may just be something else, I

am not sure what,but don't take it too personally. Jen

**************Ideas to please picky eaters. Watch video on AOL Living.

(http://living.aol.com/video/how-to-please-your-picky-eater/rachel-campos-duffy/

2050827?NCID=aolcmp00300000002598)

[Guest guest]

,

Hang in there! I have learn a tremendous amount from this board. Hope there

is some way I can help you in the future.

Colleen

Mother of Charlie 2. 5years

[ ] Re: Response to !

,

You are coming down on me for not responding to each and every

comment in your earlier post to me. I wrote that I was briefly

responding to some things based on the fact that I wanted to spend

some time with my boys before they go to bed. You are insinuating

that I'm choosing a harder road instead of choosing what " works for

most. " But haven't I already stressed that I've only just recently

joined this discussion group? Therefore, how could I have been

choosing a more difficult road when I only recently learned of your

recommended fish oil and vitamin E cocktail? You aren't even

validating the positive effects I've seen in my son from the GF/CF

diet. And I started the diet about 11 months ago....long before

joining this discussion group. And if I'd joined this discussion

group 11 months ago I'd still be searching out other help for my son

based on his extreme blow-out poops or extreme constipation....and

probably would have ended up with the DAN! doctor based on his issues

as a globablly developmentally delayed child. , I'm so sad for

you. So many of your emails don't make sense. I encourage you to go

back and read your posts. You are so quick to jump on people. You

are coming down on me for what I didn't respond to in your

email....and yet you can't make a public acknowledgement of your

error in calling methyl-B12 shots " vaccines. " You know, I've

searched many of the archives in this discussion group. I find it

interesting that years ago when you were in the earlier stages of

your journey with Tanner you wrote posts about HBOT and cranial

sacral therapy. Weren't you also a mom longing to find help (ANY

HELP) for your son? Your comments are ignorant....AND EXTREMELY

HURTFUL....to us moms with kids who ARE " TOUGH NUTS TO CRACK. " You

don't know what I've been thru since he was a baby. And now he's

almost 3. I haven't even posted everything I've been thru with

him....only the basics. So even to say that he's too young for me to

know if he's a tough nut to crack when he's getting 13 hours of

therapy every week and has been hospitalized several times....almost

died of respiratory distress..... was burned....had skin

grafting.....thought he was having seizures.....etc. etc.

ENOUGH!!!!!!!!!!!!!!! And you couldn't even give me any kind,

parting words as I did to you in my last post.

AGAIN, LISA, " WITH LOVE AND APPRECIATION FOR ALL YOU DO....FOR ALL

YOU STAND FOR......AND WITH ENVY THAT YOUR SON ONLY HAD APRAXIA OF

SPEECH "