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I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

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melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting

with a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to pick out recipes on line and in some

of the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free

to email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But

he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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Guest guest

Hi,

You have some great ideas! Would you mind sharing your basic vanilla ice cream

recipe? My son does not like the one I make.

Thanks a bunch,

Belle

jill smyth wrote:

melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting

with a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to

pick out recipes on line and in some of the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free

to email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But

he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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Jill,

What a great idea for the ice creams. What vanilla ice cream recipe do you use?

I have some dripped yogurt in the frig specificly ready to go for making some

ice cream. I'd love for you to give me the recipe. I don't think the Boreshead

hotdogs are legal though. I'm going to order a few things from Digestive

Wellness and SCD Bakery to keep in the freezer for thawing when I want to make

iel feel like he's getting something special like the family or friends

are at a party or something. Thanks for the good ideas.

Meleah

Re: HELP!!!!!!

melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting with

a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to pick out recipes on line and in some of

the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free

to email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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Guest guest

meleah, heres the recipe for the vanilla ice cream: it is based on a butter

pecan recipe i got from lucy 's kitchen shop when i ordered my ice cream maker.

I mix 1 egg, 1 tablespoon of vanilla, 1/3 cup of honey and a dash of salt into a

blender. i occasionally add a tablespoon or 2 of butter. mix this with 3 cups

of yogurt. you may need more/less vanilla and/or honey depending on your taste.

i always make it with ethan standing by to taste it and give the ok before we

put it in the freezer. I then put it in the freezer or 45 min. and then put it

in the icecream maker. I usually stir in the cookie pieces and the mint after

the icecream comes out of the ice cream maker. that way we can make 3 flavors

with one batch- vanilla, cookies and cream, and chocolate chip mint. the mint

is very strong. add a drop at a time to taste.

as for the hotdogs, i guess the questionable ingredient is the sodium

erythorbate. i believe it is derived from sugar, although i saw it labled as a

question mark on a site that gave a yes or no for listed additives for SCD. i

will try to find the site again. ethan hasn't had problems with the hotdogs,

and it has certainly helped with his adherence to the diet. of course i am

interested in what anybody else might have to say about this.

thanks very much, jill

robin wrote:

Jill,

What a great idea for the ice creams. What vanilla ice cream recipe do you use?

I have some dripped yogurt in the frig specificly ready to go for making some

ice cream. I'd love for you to give me the recipe. I don't think the Boreshead

hotdogs are legal though. I'm going to order a few things from Digestive

Wellness and SCD Bakery to keep in the freezer for thawing when I want to make

iel feel like he's getting something special like the family or friends

are at a party or something. Thanks for the good ideas.

Meleah

Re: HELP!!!!!!

melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting with

a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to pick out recipes on line and in some of

the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free to

email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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Guest guest

Thanks. I will try it in the next couple of days, and iel will get to

have ice cream while the rest of us enjoy our toxic ice cream from

Friendly's(ha, ha) while Grandpa is in town this weekend. Can you post the

ingredients for the hot dogs please?

Meleah

Re: HELP!!!!!!

melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting with

a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to pick out recipes on line and in some of

the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free

to email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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Guest guest

hi belle, i just put the recipe out on a previous email. let me know if you

don't get it. i find vanilla ice cream hard to make. i probably do it a little

different each time with ethan tasting away until it tastes good to him. i am

acutally surpised that he does like it because i still find the yogurt taste

very strong. i have thought about experimenting with saccharin, but since he

has a variety of ice cream flavors that he does like, i haven't felt the need to

yet. maybe the mint wil be strong enough to cover the flavor that your son

finds distasteful in the vanilla. best wishes, jill and ethan

Bellevox Shoemacher wrote: Hi,

You have some great ideas! Would you mind sharing your basic vanilla ice cream

recipe? My son does not like the one I make.

Thanks a bunch,

Belle

jill smyth wrote: melissa, my son ethan is 9 and would be

happy to email cole. we did give ethan money for every day he stayed on the diet

during the first 2 months. we made a special trip to target every friday. it

really helped motivate him to try new foods and feel not so deprived. i also

made a practice of buying any candy from him that he was given at school. again,

this helped him feel better about not being able to eat it. some convienance

foods that helped us were boars head hotdogs, and hamburgers wrapped in lettuce

leaves. he loves frozen juice pops, and i always keep the fridge stocked with

peanut butter fudge and a variety of yogurt icecreams. we just created chocolate

chip mint ice cream by starting with a vanilla icecream (yogurt) base, adding

crumbled Fudge Snackaroons (from Digestive Wellness) and a bit of mint extract.

Our " cookies n cream " recipe is the same, minus the mint. ethan loves to

pick out recipes on line and in some of the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free to

email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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boar's head skinless beef frankfurters ingred. beef, water, salt, paprika,

flavorings, sodium erythorbate, sodium nitrate. it says on the pkg. dairy free

and gluten free, and sugar free. all i can say is that ethan has done well on

them. i will try to make my own one of these days, when i'm not busy making

other stuff. thanks, jill

robin wrote: Thanks. I will try it in the next

couple of days, and iel will get to have ice cream while the rest of us

enjoy our toxic ice cream from Friendly's(ha, ha) while Grandpa is in town this

weekend. Can you post the ingredients for the hot dogs please?

Meleah

Re: HELP!!!!!!

melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting with

a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to pick out recipes on line and in some of

the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free to

email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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Jill,

The 'flavorings' in this product would deem it illegal, I'm afraid. It could

mean anything. We avoid any labeling that says ambigious things like:

" flavourings, seasonings, spices " These terms are just too vague and unknown.

Charlene

UC 8 years

SCD 6 1/2 years

<><

boar's head skinless beef frankfurters ingred. beef, water, salt, paprika,

flavorings, sodium erythorbate, sodium nitrate. it says on the pkg. dairy free

and gluten free, and sugar free. all i can say is that ethan has done well on

them. i will try to make my own one of these days, when i'm not busy making

other stuff. thanks, jill

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Thanks. I will try it in the next couple

of days, and

iel will get to have ice cream while the rest of us enjoy our toxic ice

cream from

Friendly's(ha, ha) while Grandpa is in town this weekend. Can you post the

ingredients for

the hot dogs please?

> Meleah

The illegal ingredients in the Boar's Head furters are " flavorings. " You

require a hand

written letter from them stating all the ingredients including what

" flavorings. "

" Gluten free' is not sufficient for SCD and the nitrates are not very healthy

for children.

Carol F.

SCD7 years, celiac

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thanks carol, i will call and see if i can get a hand written letter. i will

keep you all posted.

jill

carolfrilegh wrote:

Thanks. I will try it in the next couple of days,

and

iel will get to have ice cream while the rest of us enjoy our toxic ice

cream from

Friendly's(ha, ha) while Grandpa is in town this weekend. Can you post the

ingredients for

the hot dogs please?

> Meleah

The illegal ingredients in the Boar's Head furters are " flavorings. " You

require a hand

written letter from them stating all the ingredients including what

" flavorings. "

" Gluten free' is not sufficient for SCD and the nitrates are not very healthy

for children.

Carol F.

SCD7 years, celiac

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

Link to comment
Share on other sites

Guest guest

Well, it is technically illegal because of " flavorings " . Who knows what exactly

that entails.

Meleah

Re: HELP!!!!!!

melissa, my son ethan is 9 and would be happy to email cole. we did give ethan

money for every day he stayed on the diet during the first 2 months. we made a

special trip to target every friday. it really helped motivate him to try new

foods and feel not so deprived. i also made a practice of buying any candy from

him that he was given at school. again, this helped him feel better about not

being able to eat it. some convienance foods that helped us were boars head

hotdogs, and hamburgers wrapped in lettuce leaves. he loves frozen juice pops,

and i always keep the fridge stocked with peanut butter fudge and a variety of

yogurt icecreams. we just created chocolate chip mint ice cream by starting with

a vanilla icecream (yogurt) base, adding crumbled Fudge Snackaroons (from

Digestive Wellness) and a bit of mint extract. Our " cookies n cream " recipe is

the same, minus the mint. ethan loves to pick out recipes on line and in some of

the many scd cook books we have

bought. i let him dictate what we will eat for dinner every night. feel free

to email me anytime. we would be happy to help in anyway we can.

jill and ethan (crohn's scd 1/07)

wrote:

I know that the scdiet works!!! I have seen it work with my son. But he

refuses to keep his hands in his own lunch. I just don't know what to

do. But I need to do something. I have tried to encourage him with what

we get to eat next as well as other positive things. I have tried

scalding him, putting him on restriction (pointing out the necessity

for the diet but making the lying the reason why he is in trouble). I

have gone to the school and asked for cooperation with the staff (which

I got no problem). I have gone to the school and talked to his class to

help them understand. Nothing is working. He and other people in his

life have pushed the envelope so far for so long now that other

medication isn't working. I am a single working mom with no other

choice but for him to go to public school. I HAVE TO WORK. I am barley

affording the diet, so cant afford private school. I am at my wits end.

Any suggestions?

and Cole ( 7 years old, Crohn's 7 years, SCD 6 years, 30mg

Prednisone.)

---------------------------------

Ahhh...imagining that irresistible " new car " smell?

Check outnew cars at Yahoo! Autos.

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