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hi judith!

christopher is starting ght probably by next week too. his hormone

and pen will be here tomorrow then we have to go to chop and learn

as well. i am not thrilled about the shots either, but as you said i

will be glad that he will start to grow more. his 6 month old

brother is almost the same size as him. we dont go to our 1st dr h

appt until april, but i wanted you to know that we are learning and

starting this at the same time. we can give each other support

through this ght if you would like to email its jlcals2003@...

good luck1

jodie

(nicholas-5 nonrss, christopher-3 rss 22lbs 33 " , johnathon-6m nonrss)

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hey Judith,

Good Luck with your first GH shot! I will probably be talking to you next

month when is supposed to start! LOL Remember you lesson in button

changing??

Talk to you soon

Pat (g-ma to , RSS, 2 years old!!, 20# 5.6oz, 29.1 " , Prevacid,

Singulair, GT)

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  • 3 months later...
Guest guest

,

I am sorry if someone has already posted this idea, but we use an

ice cube. We just pick the spot, Matt prefers butt, so we alternate

sides. The ice cube dulls the skin and he takes it (usually) like a

champ!

Beth

>

> There are 24 messages in this issue.

>

> Topics in this digest:

>

> 1. CHAT Jeanine - starting GH/local Drs

> From: " pcpets "

>

> 2. ADD/ADHD - Kind of long

> From: " pcpets "

>

> 3. Re: Digest Number 2289 -

> From: " pcpets "

>

> 4. Thanks for the supportive messages!

> From: " Jodi Zwain "

> 5. Chat: Judith

> From: " Jodi Zwain "

> 6. Re: Chat: Judith

> From: " Sidny27 "

> 7. Growth Hormone Question

> From: " Carlton and "

> 8. Re: To - 6 Days on/1 Day off GH

> From: " CHRISTINE "

>

> 9. RE: Growth Hormone Question

> From: " Home "

> 10. anyone on G H please read the post in re:to jennifer

> From: " CHRISTINE "

>

> 11. Thanks everyone, problems with Xavier

> From: ljhess0701@a...

> 12. To

> From: " Jodi Zwain "

> 13. Re: Thanks everyone, problems with Xavier

> From: cara schobert

> 14. Re: Thanks everyone, problems with Xavier

> From: " Jodi Zwain "

> 15. Re: Re: To - 6 Days on/1 Day off GH

> From: cara schobert

> 16. Re: CHAT: 1st DR H. visit today

> From: " magicrss "

> 17. Re: Growth Hormone Question

> From: " magicrss "

> 18. To : Hints for GH shots

> From: " magicrss "

> 19. Re: To - 6 Days on/1 Day off GH

> From: " sherrid2003 "

> 20. Re: Facing Reality

> From: Ginger

> 21. Re: To : Hints for GH shots

> From: " CHRISTINE "

>

> 22. Re: Our School Appointment - really long post

> From: " CHRISTINE "

>

> 23. Re: Re: Thanks everyone, problems with Xavier

> From: ljhess0701@a...

> 24. Re: anyone on G H please read the post in re:to jennifer

> From: " Sidny27 "

>

>

>

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>

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>

> Message: 1

> Date: Fri, 23 Apr 2004 10:24:21 -0400

> From: " pcpets "

>

> Subject: CHAT Jeanine - starting GH/local Drs

>

> Hi Jeanine,

>

> What hospital do you use here in Cleveland? We have been using the

Cleveland

> Clinic for , but have been less than happy with the

Endocrinology

> Dept there. We found out yesterday, during a GI appt, that the

Endo we've

> been having so many problems with currently, is the Head of the

Dept, so I

> have no idea what we're going to do now.

>

> One of the biggest problems we've been running into, is that all

the Drs

> here want to do, is put on GH. They don't seem to be

concerned about

> his weight, or weight-to-height ratio. They don't worry about his

growth

> velocity, or his overall health. When we've expressed concerns

about his

> hypoglycemia, or insulin resistance, they have been less than

forthcoming

> with information, support, or a plan for handling these problems.

>

> On our first visit to the Endo Dept at the Clinic, we met Dr

. She was

> nice enough, and seemed interested in working with us, since she

has a

> couple of RSS kids already with her service. When we asked how she

felt

> about GHT, she was skeptical as to whether it would work, since

most RSS

> kids are not GHD. She told us that she would be willing to do

a " trial run "

> for 6-8 months, but if that did not yield dramatic results, she

would

> discontinue treatment. This was our first visit with her. We were

only

> asking for information. But immediately following this visit, GH

showed up

> at B's house, along with a nurse to teach everyone how to give the

shots,

> and B was started on GHT before we knew what was happening. As we

got deeper

> into our research of GH, and it's most effective use, we decided

to stop

> therapy, and revisit Dr to discuss our concerns.

>

> Research shows that GH does not rule growth in children under the

age of 2

> yrs, and that " caloric catch-up " is most important at this age.

was

> about 15 months old at the time, and was still having problems

gaining

> weight. On our second visit, we brought this fact to her

attention, and

> expressed our concerns as to whether would be able to gain

enough

> weight to keep up with a growth velocity increase of 1.5-2 times

his current

> rate. She told us that if we were going to wait for B to " catch-

up " that we

> would never be ready to start GH, and that she didn't need to see

B again,

> until we were ready to begin GHT. That was the last time we

visited her.

>

> We kept in contact with Dr H, and when she felt that B had

completed his

> caloric catch-up, and that it was time to look into starting GH,

we went in

> search of another Endo. The second endo we tried was Dr . He

is not a

> hands-on kind of guy. He seems to leave his residents to do all the

> " hands-on " work and then comes in to answer questions, etc... We

explained

> that we were in contact with an Endo in NY (Dr H) that had

extensive

> experience with RSS children, and that we were interested in

finding an Endo

> here that would be willing to collaborate with her. He stated that

he had no

> problem with this, but wondered why we weren't going to NY to use

Dr H. We

> explained that making the trip to NY was just too expensive for

our current

> financial situation.

>

> Dr had no problem with starting B on GHT either, but

expressed

> concern over some of the tests that Dr H wanted run on B before

beginning

> therapy. He promised to contact her, and told us to make an appt

with him

> for 3 months later.

>

> Three months later, we returned for our second visit with Dr

, only to

> find that he had not bothered to contact Dr H, and had gotten rid

of all the

> information we had given him on the first visit. We explained that

our

> research showed that the tests that she wanted run, were to

determine if B

> was in premature adrenarche, or insulin resistance, and why this

was

> important. He suddenly agreed to run the tests, attempted to make

us feel

> guilty for pushing the issue by stating that the amount of blood

needed for

> the extensive testing Dr H wanted would required two or more blood

draws at

> separate times, and sent us on our way. How frustrating!

>

> That was in Feb, and we still haven't been able to move forward

with the

> testing. Yesterday, we found out that the bone age scan, run on

both knees,

> was read only as an x-ray to determine whether or not B had any

> malformations, or fractures. The GI said that she's never heard of

a bone

> age scan done on the knees, and that as far as she knows, they

only use the

> hands at the Clinic, so it looks like we will be starting all over

for the

> one tests that has been completed. Talk about frustrating!

>

> I was wondering if you've had any more success with the

hospital/Drs that

> you have found here in the Cleveland area? If you like to chat, or

trade

> emails my Yahoo ID is grandmax2ab, and my email address is pcpets

> @adelphia.net (no spaces, of course)

>

> Hope to hear from you

> Pat (g-ma to , RSS, 28 months, 20# 9oz, 30.1 " , Prevacid,

Singulair,

> GT)

>

>

>

>

>

>

>

>

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>

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>

> Message: 2

> Date: Fri, 23 Apr 2004 11:15:40 -0400

> From: " pcpets "

>

> Subject: ADD/ADHD - Kind of long

>

> To all with active preschoolers

>

> ALL of the behaviors you have described with your kids, are

evident, on a

> regular basis, with my 3.5 yr old g-daughter, Aidan. Aidan does

not have

> RSS, but ADD/ADHD runs in our family genetics. Two out of 4 of my

kids were

> diagnosed with ADHD, and 5 out of the 8 cousins were/are treated

for

> ADD/ADHD.

>

> , I DO think that girls mature faster than boys, but children

with

> ADD/ADHD almost always have maturity issues. It could be that

Hayden does

> not have ADD or ADHD, and that Colin does, or it could just be

that Hayden

> is a girl and Colin is a boy. The differences in behavior would be

dramatic,

> and I totally understand having problems with not comparing the

two! It

> seemed like I wanted to ask several times a day, why one child

couldn't be

> more like the other, when mine were younger! LOL

>

> I found it interesting in 's email about Jordan knowing who

he can

> " play " and who he can't. BOTH of my ADHD kids were like that. When

> wrote about how much Jordan likes to talk, and how he can

sometimes be

> verbally unkind, it also reminded me of my two. As it was

explained to me,

> ADD/ADHD kids don't seem to have the " stop-gap " that most of us

do, that

> lets them think before the act, or reply (this falls under

impulsivity). So

> most of the time, they say, or do, the first thing that comes to

mind,

> without thinking through the consequences.

>

> One of the best treatments ever recommended for my two, was a rigid

> schedule, with a very structured routine. We did the same things

every day,

> in the same order, and in the same way, all the time. If things

got too

> rowdy, we would stop that type of play, and work on some quiet

activity,

> until they seemed calmer. We tried to get outside daily, to run off

> excessive energy. I limited the amount of refined sugar,

artificial dyes,

> and MSG in their diets. All of these seemed to cause my kids to

exhibit more

> hyper-type behavior. And when I needed them to do something, I

would get

> down at their level and make sure I had eye contact with them,

when I made

> the request. Then, I would have them repeat the request back to

me, to make

> sure they were listening. You wouldn't believe how often they

missed what I

> was saying in the beginning. As their listening skills improved,

so did

> their behavior.

>

> I hope some of these suggestions help those of you going through

this now.

> Parenting an ADD or ADHD child is frustrating, exhausting, and

exhilarating,

> all at the same time. It is wonderful to watch them learn more and

more

> self-control, as you both learn little tricks that help them focus

on the

> tasks at hand. It, also, helps them build self-esteem. It seems

like it is

> always these kids that are are getting the negative comments.

>

> It does get better with age, and even if your kids don't have

either ADD or

> ADHD, the same tricks work well with over-active preschoolers! LOL

>

> Pat (g-ma to , RSS, 28 months, 20# 19oz, 30.1 " , Prevacid,

Singulair,

> GT)

>

>

>

>

>

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>

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>

> Message: 3

> Date: Fri, 23 Apr 2004 11:19:36 -0400

> From: " pcpets "

>

> Subject: Re: Digest Number 2289 -

>

> Hi ,

>

> It is so great to hear that Dennis is doing so well now. He's been

through

> so much since i joined the list serve a year and a half ago! Glad

to hear

> that he'll be able to get back to hockey soon! Been through that

aggressive

> male puberty stage, and there's nothing like athletics to expend

it on! LOL

>

> Good to hear from you!

> Pat (g-ma to , RSS, 28 months, 20# 9oz, 30.1 " , Prevacid,

Singulair,

> GT)

>

>

>

>

>

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>

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>

> Message: 4

> Date: Fri, 23 Apr 2004 18:44:44 -0000

> From: " Jodi Zwain "

> Subject: Thanks for the supportive messages!

>

> Hi, everyone. I cannot tell you how much I appreciate your

> supportive messages regarding our decision with Max's education.

It

> was a hard one to make and I was really nervous, but I think it

will

> work out. I'm so glad that you all care enough and that I can turn

> to you for advice and a virtual shoulder to cry on.

>

> I have since spoken to the Director of Special Services, the high

> school psychologist/Max's case manager, and Max's history and math

> teacher (he's the teacher for both subjects). Max is going to stay

> in classes until 11:45 each day. If he is not feeling well, he can

> go to the nurse's office and rest until he feels well enough to go

> back to class. Basically, in that time period, Max has study

> skills, digital photography, study hall, history and math. If he

is

> unable to complete history or math, then the teacher will give him

> work to do at home. Home instruction will be in English.

>

> Max knows that he will come home, take a break/rest and then have

to

> do reading and some chores. He is not coming home to watch TV for

> the rest of the day. And he will get home instruction three days a

> week.

>

> Hopefully this will get Max on track for the rest of the school

> year, which is less than two months anyway. And hopefully he will

> feel better and be able to build up his strength. (BTW, when he

has

> his button placed next week, he will also be tested for the H

Pylori

> infection.)

>

> Thanks again, everyone. You are a wonderful group!

>

> Jodi Z.

>

>

>

>

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>

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>

> Message: 5

> Date: Fri, 23 Apr 2004 18:49:30 -0000

> From: " Jodi Zwain "

> Subject: Chat: Judith

>

> Judith,

>

> It seems like you have your bases covered for next year.

> You've done a great job. It is so scary and overwhelming in the

> special educational system - and the No Child Left Behind Act is

> making it even harder.

>

> I do have one question. Why are they calling 's class

> a " segregated " class? Here it is called a self-contained class.

> Segregated sounds so awful!

>

> To answer your question about thinking in advance with Max's IEP

and

> possible home instruction, it just seemed like a natural thing to

> include considering Max's health history. I happen to think that

> any child, RSS or not, who is at risk for hospitalizations due to

> stomach viruses, hypoglycemia, surgery, etc. should automatically

> have that included in the IEP. You don't have to implement it

> unless it is needed and it sure speeds up the process when it is

> required. Without that part in Max's IEP, the district could have

> said no to our request or they would have had to go through

revising

> Max's IEP and that would take a long time to do.

>

> Just something to think about for those who are going through the

> IEP process for the first time or making up new ones for next

year.

> Better to have it and not use it than to not have it at all.

>

> Jodi Z.

>

>

>

>

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>

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>

> Message: 6

> Date: Fri, 23 Apr 2004 19:23:25 -0000

> From: " Sidny27 "

> Subject: Re: Chat: Judith

>

> Hi Jodi,

>

> I guess it really is called self-contained, I was just half asleep

> this morning.

>

> So far, other than overnight for tonsils (as a precaution),

has

> not been in the hospital since the gtube etc. in June 2002.

> Something to consider for the future, but not for preschool next

year

> since his IEP is already done.

>

> Thanks for letting me know I'm on top of things. I think I just

> needed validation for someone who has been there that I'm not

> forgetting anything important.

>

> Hang in there with Max,

>

> Judith

>

>

>

>

>

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>

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>

> Message: 7

> Date: Fri, 23 Apr 2004 20:05:59 -0000

> From: " Carlton and "

> Subject: Growth Hormone Question

>

> had started her growth hormone of .5 in Oct 2003. We saw

> her doctor who is Dr. here at Ft. Hood on the 14th of

April.

> He said that there had been no significant change in her growth as

> far as height or weight in 6 months. He had explained to us that

if

> given the dosage everyday with the exception of Saturday which is

her

> day off the shot she should have shown an increase in (1) her shoe

> size and (2) appetite. She has been with my husband and I for 3

wks

> now and she has had an enormous change in appetite. She is eating

> everything!!! Her and her brothers and sisters have a love for

> vegetables which is wonderful because not very many children do.

We

> started giving her 2 vitamins a day. We make sure she has extra

> calcium and protein as well.

> Since Dr. has talked to us about how important making

> sure that if she is on the shot it must be consistant. She was

given

> her shot every day she was supposed to in our care and if it is

> recommended by her doctor to try the shot again we will make sure

> while under our care it is done. She was very brave when she took

her

> shots and we are so proud of how she has been dealing with it all.

We

> are scheduled to see a nutritionist soon.

> Our main issue with her taking the GH shot is that once she

> started taking it that it wasn't going to be all for nothing. We

hate

> her having to get shots and nothing positive come from it. She has

> been off the shot now for 9 days and has not lost any weight from

not

> taking it. She is active and healthy. We are hoping that the GH

shot

> will be something we can try again and have a positive outcome in

the

> near future for her. Has any other parents gone through the same

> thing with the GH shot. Does it take longer than 6 months to show

any

> change in some children? I figure it is different with each child.

> and Carlton

>

>

>

>

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>

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>

> Message: 8

> Date: Fri, 23 Apr 2004 20:39:38 -0000

> From: " CHRISTINE "

>

> Subject: Re: To - 6 Days on/1 Day off GH

>

> - Hi this is s mom, I know you wrote this

to

> , but We have started G H 3 days ago and we are doing the

> same as you 6 times a week and one day off, I am picking Saturdays

> for the day off, you said Abby is doing good, is she used to

doctors

> and being poked alot? is going hysterical on me when

giving

> the shot, I feel so bad for him, I think he thought he was going

to

> only get the shot at the doctors that day and now he realizes that

we

> are doing it at home, he is totally freaking out on me, I think

the

> reason is because he has been through so much, 2 surgeries on his

> penis for hypospadias, he has had to be put to sleep to many times

> for an endoscope and colonoscopy..tubes in ears and well there is

> more it seems like when he gets sick we are back to the hospital

and

> all he knows is getting poked or at just a sick appointment he

ends

> up having to get poked for blood.He is not at all happy about this

> and now I feel like he is tramatized!!! I have talked with him

about

> it and try to get him to help do the alcohol swab ...but when he

> knows it is fixing to happen he goes nuts and starts crying before

I

> even get the shot ready!! He knows that we are going to either do

it

> before bath then he doesn't want to take a bath or if he knows

that

> we are going to do it after bath then he screams and doesn't want

to

> get out! The look in his little eyes hurts me so bad and I am

really

> getting sad for him but I know I have to be strong, do you have

any

> advice, I know I can do it but I am so depressed right now for

fear

> he is going to hate me!! He yells at me and calls me meanie and it

> hurts to see him like this?? Well sorry this is so long but just

in

> need of help, he also has to go to the doctor and get his shots

for

> kindergarten and the are going to have to give him 3 what if I

have

>

> === message truncated ===

>

>

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