Jump to content
RemedySpot.com

Re: Hallo from Greece!

Rate this topic


Guest guest

Recommended Posts

ekali08 wrote:

> Hallo!

> This is my first time chatting about RSS , so i have so much to talk

>to , that i have to put everything in order!

>

>I was wondering about 2006 convention of Magic Foundation,if its worth

>it to go there all the way from Greece (Europe) and also to ask if any

>other people from Greece have ever attended such a convention in the

>previous years? It would be such a great help for me to be able to

>communicate with them .

>

>My doughter Arianna is 10 years old and she just started Growth Hormone

>Therapy.I was trying for the last three years to give her the GH therapy

>but there were barriers all over , so we found our way out a month ago.

>I m so glad she started this therapy- hoping that it will give her

>extra height and mass weigth - but on the other hand very worried about

>the side effects although i 've read over and over again that there are

>not any.

>

>Thank you for listening and i'll be very glad to communicate with

>whoever is interested !

>

>Ada

>

>

>

>

>

>

>

>

Link to comment
Share on other sites

Hi Ada,

Welcome to oyr group. I hope we can answer your questions.

I have been thinking about your question on whether it is worthwhile

for you to attend the convention from Greece. There is no simple

answer. It depends. First it depends on how well your daughter is

doing and on whether or not any of the presentations can help you.

That is one thing to consider. The other is will it be woth your

while to meet with about 100 other families who have children with

RSS, some are infants and some are almost grown.

I would think it might be beneficial to for you to come to at least

one convention and meet with as many families as you can.

There are some side affects to growth hormone but they seem rare.

They are mostly joint pain and/or headaches. In either case you

should stop using the growth hormone until you can get to see a

doctor.

I hope this helps make a decision about coming to Chicago or not.

Please feel free to ask us anything. Someone usually has an opinion.

Ken M

:)

>

> Hallo!

> This is my first time chatting about RSS , so i have so much to

talk

> to , that i have to put everything in order!

>

> I was wondering about 2006 convention of Magic Foundation,if its

worth

> it to go there all the way from Greece (Europe) and also to ask if

any

> other people from Greece have ever attended such a convention in

the

> previous years? It would be such a great help for me to be able to

> communicate with them .

>

> My doughter Arianna is 10 years old and she just started Growth

Hormone

> Therapy.I was trying for the last three years to give her the GH

therapy

> but there were barriers all over , so we found our way out a month

ago.

> I m so glad she started this therapy- hoping that it will give her

> extra height and mass weigth - but on the other hand very worried

about

> the side effects although i 've read over and over again that there

are

> not any.

>

> Thank you for listening and i'll be very glad to communicate with

> whoever is interested !

>

> Ada

>

Link to comment
Share on other sites

Hello, Ada. I am new to this site as well. My 15 mo. old son was diagnosed in

November. We live in a very small town in the state of New York in the United

States. I can't be of much help to you, unfortunately, since this is all new to

me. I am hoping to attend the convention in July as well. Finances will be our

issue. I left my job after my son, Brockton, was born in August of 2004. I

have an 18 yr. old daughter as well and she is very healthy. Actually, my

children are on absolute opposite ends of the spectrum! She battles obesity,

unfortunately. I KNOW that runs in the family as we have a long line of over

weight people, including myself.

When was your daughter diagnosed with RSS? I'm always interested in hearing

other peoples stories. It gives me insight and understanding. The nearest

decent hospital is 2 hrs. away from us and they don't have any Dr.'s that know

much about RSS. I'm hoping to get in to see Dr. Harbison as soon as the results

from Brocktons growth hormone tests come back in about a week. What a time they

had trying to draw his blood yesterday! Brockton was a MESS. His skin is so

thin that they tore it with the needle in one hand and blew the vein. They had

to do his other little hand after that and were quite successful with that one,

thank God.

I wish I could be of more help to you but I know that there of plenty of

people on this site that are, in my opinion, more helpful than alot of the

Dr.'s.

Good luck to you and your family!

Jeanie

ekali08 wrote:

Hallo!

This is my first time chatting about RSS , so i have so much to talk

to , that i have to put everything in order!

I was wondering about 2006 convention of Magic Foundation,if its worth

it to go there all the way from Greece (Europe) and also to ask if any

other people from Greece have ever attended such a convention in the

previous years? It would be such a great help for me to be able to

communicate with them .

My doughter Arianna is 10 years old and she just started Growth Hormone

Therapy.I was trying for the last three years to give her the GH therapy

but there were barriers all over , so we found our way out a month ago.

I m so glad she started this therapy- hoping that it will give her

extra height and mass weigth - but on the other hand very worried about

the side effects although i 've read over and over again that there are

not any.

Thank you for listening and i'll be very glad to communicate with

whoever is interested !

Ada

Link to comment
Share on other sites

Hello, Ada. I am new to this site as well. My 15 mo. old son was diagnosed

in November. We live in a very small town in the state of New York in the

United States. I can't be of much help to you, unfortunately, since this is all

new to me. I am hoping to attend the convention in July as well. Finances will

be our issue. I left my job after my son, Brockton, was born in August of 2004.

I have an 18 yr. old daughter as well and she is very healthy. Actually, my

children are on absolute opposite ends of the spectrum! She battles obesity,

unfortunately. I KNOW that runs in the family as we have a long line of over

weight people, including myself.

When was your daughter diagnosed with RSS? I'm always interested in hearing

other peoples stories. It gives me insight and understanding. The nearest

decent hospital is 2 hrs. away from us and they don't have any Dr.'s that know

much about RSS. I'm hoping to get in to see Dr. Harbison as soon as the results

from Brocktons growth hormone tests come back in about a week. What a time they

had trying to draw his blood yesterday! Brockton was a MESS. His skin is so

thin that they tore it with the needle in one hand and blew the vein. They had

to do his other little hand after that and were quite successful with that one,

thank God.

I wish I could be of more help to you but I know that there of plenty of

people on this site that are, in my opinion, more helpful than alot of the

Dr.'s.

Good luck to you and your family!

Jeanie

ekali08 wrote:

Hallo!

This is my first time chatting about RSS , so i have so much to talk

to , that i have to put everything in order!

I was wondering about 2006 convention of Magic Foundation,if its worth

it to go there all the way from Greece (Europe) and also to ask if any

other people from Greece have ever attended such a convention in the

previous years? It would be such a great help for me to be able to

communicate with them .

My doughter Arianna is 10 years old and she just started Growth Hormone

Therapy.I was trying for the last three years to give her the GH therapy

but there were barriers all over , so we found our way out a month ago.

I m so glad she started this therapy- hoping that it will give her

extra height and mass weigth - but on the other hand very worried about

the side effects although i 've read over and over again that there are

not any.

Thank you for listening and i'll be very glad to communicate with

whoever is interested !

Ada

Link to comment
Share on other sites

  • 2 weeks later...

Jeanie,

Are you in upstate NY? Where are you? The only places in upstate I can

relate to are Penn Yan and Tuxedo NY which is just over the NJ border. Did you

get the results yet from Brockton's test?

B

and Kelli

Jeanie Kinnicutt wrote:

Hello, Ada. I am new to this site as well. My 15 mo. old son was diagnosed

in November. We live in a very small town in the state of New York in the

United States. I can't be of much help to you, unfortunately, since this is all

new to me. I am hoping to attend the convention in July as well. Finances will

be our issue. I left my job after my son, Brockton, was born in August of 2004.

I have an 18 yr. old daughter as well and she is very healthy. Actually, my

children are on absolute opposite ends of the spectrum! She battles obesity,

unfortunately. I KNOW that runs in the family as we have a long line of over

weight people, including myself.

When was your daughter diagnosed with RSS? I'm always interested in hearing

other peoples stories. It gives me insight and understanding. The nearest

decent hospital is 2 hrs. away from us and they don't have any Dr.'s that know

much about RSS. I'm hoping to get in to see Dr. Harbison as soon as the results

from Brocktons growth hormone tests come back in about a week. What a time they

had trying to draw his blood yesterday! Brockton was a MESS. His skin is so

thin that they tore it with the needle in one hand and blew the vein. They had

to do his other little hand after that and were quite successful with that one,

thank God.

I wish I could be of more help to you but I know that there of plenty of

people on this site that are, in my opinion, more helpful than alot of the

Dr.'s.

Good luck to you and your family!

Jeanie

ekali08 wrote:

Hallo!

This is my first time chatting about RSS , so i have so much to talk

to , that i have to put everything in order!

I was wondering about 2006 convention of Magic Foundation,if its worth

it to go there all the way from Greece (Europe) and also to ask if any

other people from Greece have ever attended such a convention in the

previous years? It would be such a great help for me to be able to

communicate with them .

My doughter Arianna is 10 years old and she just started Growth Hormone

Therapy.I was trying for the last three years to give her the GH therapy

but there were barriers all over , so we found our way out a month ago.

I m so glad she started this therapy- hoping that it will give her

extra height and mass weigth - but on the other hand very worried about

the side effects although i 've read over and over again that there are

not any.

Thank you for listening and i'll be very glad to communicate with

whoever is interested !

Ada

Link to comment
Share on other sites

Hi Ada. We got the results for the GH tests back but not the Chromozome tests.

The GH tests came back normal. We are located on the Pennsylvania

border.....about 2 hours Southeast of Buffalo, NY. South of Penn Yan as well,

actually. We live in Wellsville, NY. I've never heard of Tuxedo. LOL (I

don't get out much.) We are 2 and a half hours West of Binghamton, NY.

How is Arianna doing? I trust that your holidays are happy. Do you celebrate

Christmas in Greece? What do you do for New Years?

Great to hear from you again.

Jeanie

Briggs wrote:

Jeanie,

Are you in upstate NY? Where are you? The only places in upstate I can

relate to are Penn Yan and Tuxedo NY which is just over the NJ border. Did you

get the results yet from Brockton's test?

B

and Kelli

Jeanie Kinnicutt wrote:

Hello, Ada. I am new to this site as well. My 15 mo. old son was diagnosed

in November. We live in a very small town in the state of New York in the

United States. I can't be of much help to you, unfortunately, since this is all

new to me. I am hoping to attend the convention in July as well. Finances will

be our issue. I left my job after my son, Brockton, was born in August of 2004.

I have an 18 yr. old daughter as well and she is very healthy. Actually, my

children are on absolute opposite ends of the spectrum! She battles obesity,

unfortunately. I KNOW that runs in the family as we have a long line of over

weight people, including myself.

When was your daughter diagnosed with RSS? I'm always interested in hearing

other peoples stories. It gives me insight and understanding. The nearest

decent hospital is 2 hrs. away from us and they don't have any Dr.'s that know

much about RSS. I'm hoping to get in to see Dr. Harbison as soon as the results

from Brocktons growth hormone tests come back in about a week. What a time they

had trying to draw his blood yesterday! Brockton was a MESS. His skin is so

thin that they tore it with the needle in one hand and blew the vein. They had

to do his other little hand after that and were quite successful with that one,

thank God.

I wish I could be of more help to you but I know that there of plenty of

people on this site that are, in my opinion, more helpful than alot of the

Dr.'s.

Good luck to you and your family!

Jeanie

ekali08 wrote:

Hallo!

This is my first time chatting about RSS , so i have so much to talk

to , that i have to put everything in order!

I was wondering about 2006 convention of Magic Foundation,if its worth

it to go there all the way from Greece (Europe) and also to ask if any

other people from Greece have ever attended such a convention in the

previous years? It would be such a great help for me to be able to

communicate with them .

My doughter Arianna is 10 years old and she just started Growth Hormone

Therapy.I was trying for the last three years to give her the GH therapy

but there were barriers all over , so we found our way out a month ago.

I m so glad she started this therapy- hoping that it will give her

extra height and mass weigth - but on the other hand very worried about

the side effects although i 've read over and over again that there are

not any.

Thank you for listening and i'll be very glad to communicate with

whoever is interested !

Ada

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...