Jump to content
RemedySpot.com

Jodi R

Rate this topic


Guest guest

Recommended Posts

Guest guest

Jodi R -- just a quick note as I am trying to get through the

zillion postings. I loved reading your update on . Don't

worry too much about the not eating, since he is on tube feedings 22

hours a day. The fact is (and we learned this painfully with

and her TPN feeds), while they are on tube feedings that are

continuous, they simply won't be hungry to eat most of the time.

Experts say to keep offering finger foods -- cheerios, etc. to keep

their oral mouth working. We had to get 's weight to about 3-

4 pounds ABOVE ideal, and then stop the feeds cold turkey. I have

heard other families have gone to nighttime feeds first, and then

bolus feeds only. At the convention, there is a 3-hour feeding

session, and I know many parents want to talk about weaning from a G-

tube!

> Yah! I am sooo glad you remembered! :o) is actually

doing

> alright right now. I was reading the posts from the last few days

> and was into the controversial ones about posting some good things

> our kids are doing too. Let me just announce that is

WALKING

> now. He started right before his 2nd birthday, which was May

23rd.

> And let me also say, he is walking like he has done it for

months! I

> couldn't believe how one day he was scared to take even one step,

> then the next day it was six steps, the next it was 20, then that

is

> ALL she wrote. I haven't been able to keep up with him since!

Hee,

> hee. He has an IV pole that I have to push right behind him since

he

> is g tube fed 22 hours out of the day. Yes, I said 22. We went

from

> 23 hours to 22 hours a day. His pediatrician has GRANTED us an

extra

> hour off to try to feed some REAL food! I am so glad he

has

> two hours off now, because that one hour a day went faster than

you

> would believe. Since he is walking now, he can have two hours of

> freedom from his stupid pole and us being two steps behind him.

As

> for the feeding him REAL food......hmmm, not so well, really. He

> only wants to take a few bites. Some day he will only take one

bite

> and say, " All done. " I am like, " What? No way. More bites

> please. " He's like, " ALL DONE! " So, it is not going all that

well,

> but maybe he is still even kinda full after two hours off, since

he

> is fed the other 22 hours. I don't know. Maybe I am just making

> excuses. But, his weight is doing pretty well right now, compared

to

> his height. He is 28 " long and 18 lbs. 6 oz as of last Tuesday.

His

> ped. said he was at the 25th percentile for weight vs. height.

> Anyone verify that?? :o) But, for the most part, has made

> HUGE improvements in the last few months, after seeing Dr. H. So,

I

> owe her BIG time. If you saw a picture of from his last

> birthday and compare it to this year, you would not beleive it was

> the same kid.

>

> So, my message here today has a little of frustration to it, and a

> little of the good news too. I am still VERY annoyed with the

tube

> feedings, and get down and wonder if my little guy will EVER get

away

> from it. Especially when he is walking and so happy when he can

go

> off by himself and not have to worry about getting too far from

his

> pole. Plus, let me add a little self pity here. It is hard for

us

> to be there with every step he takes, because we do have another

> child and stuff to do around here. So, that brings me to my next

> thought/question. Does any one have any suggestions for what I

can

> do with 's pump and feeding bag to allow him more

> independence? I know some of the kids get back packs, but I

wonder

> if it will be too heavy for him. Pat, I know got one.

How

> big was he when he got his. Should I email Dr. H and tell her

> is walking and see if she could bring him a backpack to the

> convention?

>

> So, Sharon, I am sure you are sorry you asked how is

> doing! :o) I just had so much on my mind, especially after

reading

> the latest posts, that I guess I went on rambling. Yes, another

LONG

> post by me! :o)

>

> Oh yeah, and is talking very well. The thing with him and

his

> milestones seem to be this. Yes, was one of the RSS kids

that

> hit his milestones late. Especially gorss motor skills. Like I

> said, he wasn't walking until 23 months, but his language skills

have

> always seemed to be within the range. But, once he got the skill

> down, he took it to a whole new level, like he had been doing it

for

> a while. It just took him some time to get it down. His

therapists

> are amazed by him each time they see him. They introduce

something

> new to him he can't do that week, but the next week he is doing it

> like an old pro. As for the talking, he is saying things that we

> don't say. He just puts words together on his won, and we are

> shocked by it.

>

> So, that is my update on . We are still fighting with the

bad

> weight gain, thus the 22 hour feeds plus trying to feed him

orally,

> but we are also in the midst of perfection with his talking and

> walking. I am so proud that we took him to New York to see Dr. H.

> and to see the INCREDIBLE progress he made because of that one

trip.

> I have to say, it was a VERY frustrating and nerve racking trip,

and

> I questioned why I went in the first place, but to see him now is

a

> testament as to why I want to go to convention and see her again.

I

> am hoping that there will be goods news from her and that she will

> also be pleased with his progress. I wish I could express to you

all

> just how much difference has been made in him. It truly is

amazing.

> He was one of the RSS kids that had trouble holding up his head.

> Shoot, for the longest time his head was HALF his body weight. It

> was really unproportionate to his body. After going to New York

and

> putting on some weight, he was able to hold his own head up and

start

> seeing the world upright, instead of laying down.

>

> Anyway, I am proud of , and the strides that he has made. I

am

> sorry this is so long, since I haven't been on here lately I have

so

> much to tell everyone. I hope you can forgive me with this LONG

> post, just this once. I wanted to add some positives and show

people

> waht a HUGE difference can really happen in our kids.

wasn't

> diagnosed with RSS until 17 months old, and prior to that, we ad

so

> many questions, and even wondered what his life was going to be

> like. Now I know that he will be fine. Just a few fedding

issues,

> and weight and height issues to overcome, but he will rteally be

> fine. Just like Sharon is! You are such an inspiration. I told

you

> that before, and I always hoped was going to be fine, too.

> And, now I know he will be. He is really on the path to be

> a " regular " kid! :o)

>

> Sorry so long, guys,

> Jodi R.

> One proud momma

> 18 lbs. 6 oz., 28 " , Prilosec

Link to comment
Share on other sites

Guest guest

,

Thanks for your response. Man, I sure hope I signed up for that

feeding session! I would LOVE to be able to go to just night time

feeds or whatever. But, really, it will be whatever Dr. H

recommends. I mean, after all, she is the one that brought to

where he is now!

Jodi

> > Yah! I am sooo glad you remembered! :o) is actually

> doing

> > alright right now. I was reading the posts from the last few

days

> > and was into the controversial ones about posting some good

things

> > our kids are doing too. Let me just announce that is

> WALKING

> > now. He started right before his 2nd birthday, which was May

> 23rd.

> > And let me also say, he is walking like he has done it for

> months! I

> > couldn't believe how one day he was scared to take even one step,

> > then the next day it was six steps, the next it was 20, then that

> is

> > ALL she wrote. I haven't been able to keep up with him since!

> Hee,

> > hee. He has an IV pole that I have to push right behind him

since

> he

> > is g tube fed 22 hours out of the day. Yes, I said 22. We went

> from

> > 23 hours to 22 hours a day. His pediatrician has GRANTED us an

> extra

> > hour off to try to feed some REAL food! I am so glad he

> has

> > two hours off now, because that one hour a day went faster than

> you

> > would believe. Since he is walking now, he can have two hours of

> > freedom from his stupid pole and us being two steps behind him.

> As

> > for the feeding him REAL food......hmmm, not so well, really. He

> > only wants to take a few bites. Some day he will only take one

> bite

> > and say, " All done. " I am like, " What? No way. More bites

> > please. " He's like, " ALL DONE! " So, it is not going all that

> well,

> > but maybe he is still even kinda full after two hours off, since

> he

> > is fed the other 22 hours. I don't know. Maybe I am just making

> > excuses. But, his weight is doing pretty well right now,

compared

> to

> > his height. He is 28 " long and 18 lbs. 6 oz as of last Tuesday.

> His

> > ped. said he was at the 25th percentile for weight vs. height.

> > Anyone verify that?? :o) But, for the most part, has

made

> > HUGE improvements in the last few months, after seeing Dr. H.

So,

> I

> > owe her BIG time. If you saw a picture of from his last

> > birthday and compare it to this year, you would not beleive it

was

> > the same kid.

> >

> > So, my message here today has a little of frustration to it, and

a

> > little of the good news too. I am still VERY annoyed with the

> tube

> > feedings, and get down and wonder if my little guy will EVER get

> away

> > from it. Especially when he is walking and so happy when he can

> go

> > off by himself and not have to worry about getting too far from

> his

> > pole. Plus, let me add a little self pity here. It is hard for

> us

> > to be there with every step he takes, because we do have another

> > child and stuff to do around here. So, that brings me to my next

> > thought/question. Does any one have any suggestions for what I

> can

> > do with 's pump and feeding bag to allow him more

> > independence? I know some of the kids get back packs, but I

> wonder

> > if it will be too heavy for him. Pat, I know got one.

> How

> > big was he when he got his. Should I email Dr. H and tell her

>

> > is walking and see if she could bring him a backpack to the

> > convention?

> >

> > So, Sharon, I am sure you are sorry you asked how is

> > doing! :o) I just had so much on my mind, especially after

> reading

> > the latest posts, that I guess I went on rambling. Yes, another

> LONG

> > post by me! :o)

> >

> > Oh yeah, and is talking very well. The thing with him and

> his

> > milestones seem to be this. Yes, was one of the RSS kids

> that

> > hit his milestones late. Especially gorss motor skills. Like I

> > said, he wasn't walking until 23 months, but his language skills

> have

> > always seemed to be within the range. But, once he got the skill

> > down, he took it to a whole new level, like he had been doing it

> for

> > a while. It just took him some time to get it down. His

> therapists

> > are amazed by him each time they see him. They introduce

> something

> > new to him he can't do that week, but the next week he is doing

it

> > like an old pro. As for the talking, he is saying things that we

> > don't say. He just puts words together on his won, and we are

> > shocked by it.

> >

> > So, that is my update on . We are still fighting with the

> bad

> > weight gain, thus the 22 hour feeds plus trying to feed him

> orally,

> > but we are also in the midst of perfection with his talking and

> > walking. I am so proud that we took him to New York to see Dr.

H.

> > and to see the INCREDIBLE progress he made because of that one

> trip.

> > I have to say, it was a VERY frustrating and nerve racking trip,

> and

> > I questioned why I went in the first place, but to see him now is

> a

> > testament as to why I want to go to convention and see her

again.

> I

> > am hoping that there will be goods news from her and that she

will

> > also be pleased with his progress. I wish I could express to you

> all

> > just how much difference has been made in him. It truly is

> amazing.

> > He was one of the RSS kids that had trouble holding up his head.

> > Shoot, for the longest time his head was HALF his body weight.

It

> > was really unproportionate to his body. After going to New York

> and

> > putting on some weight, he was able to hold his own head up and

> start

> > seeing the world upright, instead of laying down.

> >

> > Anyway, I am proud of , and the strides that he has made.

I

> am

> > sorry this is so long, since I haven't been on here lately I have

> so

> > much to tell everyone. I hope you can forgive me with this LONG

> > post, just this once. I wanted to add some positives and show

> people

> > waht a HUGE difference can really happen in our kids.

> wasn't

> > diagnosed with RSS until 17 months old, and prior to that, we ad

> so

> > many questions, and even wondered what his life was going to be

> > like. Now I know that he will be fine. Just a few fedding

> issues,

> > and weight and height issues to overcome, but he will rteally be

> > fine. Just like Sharon is! You are such an inspiration. I told

> you

> > that before, and I always hoped was going to be fine,

too.

> > And, now I know he will be. He is really on the path to be

> > a " regular " kid! :o)

> >

> > Sorry so long, guys,

> > Jodi R.

> > One proud momma

> > 18 lbs. 6 oz., 28 " , Prilosec

Link to comment
Share on other sites

  • 5 months later...

hi saundra!!

i got an email from jodi r 2 weeks ago with a new email address, i

emailed her back and then she did the same. but this weekend i

tried to email her at the same address again and it got returned!!!

i am a little worried so if anyone hears anything or jodi r if you

read this from your parents house please contact me some how!!!

jodie c.

- In RSS-Support , " momtodandb " <cspendlet@c...>

wrote:

>

> Hi,

> I was wondering if anyone has been in touch with Jodi Rollison?

Her

> email and cell phone are no longer working and I haven't been able

> to touch base with her. Thank you for any info.

>

> Saundra Mom to Braeden (RSS) and Delaney 25 month twins who are

> currently emptying the paper shredder recycle bin.

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...