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Mara,

Are you in the support group in the triangle area? Or are you in

another part of the state? So sad to hear about the death of the mom

and child.

Elaine in Raleigh

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Mara, where are you in NC? We are in Columbus County.

So sorry to hear about the mother and her child--how tragic.

Robin T. in NC

>

> I don't tend to write on the list, mostly lurk really, but my husband

> and I

> went to the Conference (we just got back from our drive home) and I wanted

> to share a few thoughts. At the opening session, the teen group did a skit

> showing how they can do anything they want regardless of the hearing loss.

> It was full of funny lines but I sobbed through the whole thing. I was

> just

> so touched by how well they were doing and how 'typical' and happy they

> were!

>

> I got to meet a mom whose name I've seen on the listserv and that was just

> wonderful. It was fun to connect with someone you feel like you know just

> b/c you've read your email! (Thanks Deganit).

>

> I loved learning about all the new technology - what is out now and what

> is

> coming. My daughter is only 2 and already her hearing aids while good are

> not the newest hi-tech deal out there. I feel really optimistic about what

> the future in hearing aids holds (and CIs if she goes that route someday).

> Of course, I stuffed my bags with endless pens, cups, keychains, etc and

> am

> now wondering why! You kind of get carried away in those exhibit halls.

>

> Finally, I learned so much. I went to some really good speakers -

> highlights for me were Carol Flexer's talks (I only knew to go hear her

> b/c

> of this listserv) and one from Clinic's staff on play and

> social

> interactions (tips on how to help our kids socially).

>

> It was very powerful being there surrounded by people who knew what I was

> feeling and going through as a mom. Professionals who cared enough to go

> into this field and to keep their knowledge current. And deaf and hard of

> hearing adults who were living their lives happily and successfully.

>

> On a totally different and very tragic note, I came home to really

> horrible

> news. We are part of a family support group for parents of kids with HL.

> One of our moms and her two year old son died this weekend in a car

> accident. Life is so fleeting and I am so grateful for my family, friends,

> the parent group here in North Carolina, and all of you.

>

> Mara

>

> (mom of Ally, 2 yo, HA)

>

>

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Mara - I'm so sorry to hear about the loss of the mom and child in your

group - how awful!

I'm so glad you got to go to AG Bell! I remember going to our first

e mainstream conference. It's held yearly in Springfield Mass and

is excellent - and affordable! There are scholarships available usually

for first-time parents to the conference. I think I cried the entire

time - it hit home! Luterman and Donna Sorkin were the two

keynote speakers and the " famous speaker " at the end of Day 2 was Curtis

Pride. What a story he has to tell! I remember just sobbing through

his whole talk thinking that surely my boys could also lead happy,

productive lives. It was so great so meet other Listen-up parents and

to get to talk to vendors - as a parent, we usually aren't able to do

that... I'm glad it was good for you!

Hugs,

Barbara

marabd wrote:

> I don't tend to write on the list, mostly lurk really, but my husband and I

> went to the Conference (we just got back from our drive home) and I wanted

> to share a few thoughts. At the opening session, the teen group did a skit

> showing how they can do anything they want regardless of the hearing loss.

> It was full of funny lines but I sobbed through the whole thing. I was just

> so touched by how well they were doing and how 'typical' and happy they

> were!

>

>

>

> I got to meet a mom whose name I've seen on the listserv and that was just

> wonderful. It was fun to connect with someone you feel like you know just

> b/c you've read your email! (Thanks Deganit).

>

>

>

> I loved learning about all the new technology - what is out now and what is

> coming. My daughter is only 2 and already her hearing aids while good are

> not the newest hi-tech deal out there. I feel really optimistic about what

> the future in hearing aids holds (and CIs if she goes that route someday).

> Of course, I stuffed my bags with endless pens, cups, keychains, etc and am

> now wondering why! You kind of get carried away in those exhibit halls.

>

>

>

> Finally, I learned so much. I went to some really good speakers -

> highlights for me were Carol Flexer's talks (I only knew to go hear her b/c

> of this listserv) and one from Clinic's staff on play and social

> interactions (tips on how to help our kids socially).

>

>

>

> It was very powerful being there surrounded by people who knew what I was

> feeling and going through as a mom. Professionals who cared enough to go

> into this field and to keep their knowledge current. And deaf and hard of

> hearing adults who were living their lives happily and successfully.

>

>

>

> On a totally different and very tragic note, I came home to really horrible

> news. We are part of a family support group for parents of kids with HL.

> One of our moms and her two year old son died this weekend in a car

> accident. Life is so fleeting and I am so grateful for my family, friends,

> the parent group here in North Carolina, and all of you.

>

>

>

> Mara

>

> (mom of Ally, 2 yo, HA)

>

>

>

>

>

>

>

>

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Guest guest

I live in Durham, NC and yes, we attend the Hitch-up (Hearing impaired

children and teens have unlimited potential) group that meets in Raleigh.

One nice part of the group is that the audiology students at our local

university volunteer and provide childcare at the meeting (once a month).

We use UNC for our audiology/ENT so I've been glad to see how well it's been

going for Robin (I think!) with Pat Roush and Dr. Buchman. We love them

both and have seen them since my daughter was identified at birth.

We are going to the visitation today for the mom/son who passed away in the

car accident. I can't stop looking at my daughter/husband and feeling so

sad for this dad. His little son wore HA and was only a few days apart in

age from my daughter.

Thanks to the group for 'listening' to my thoughts on the conference. It

was a lovely experience and maybe we can make it to a e conference next

time.

Mara

Re: AG Bell conference feelings

Mara - I'm so sorry to hear about the loss of the mom and child in your

group - how awful!

I'm so glad you got to go to AG Bell! I remember going to our first

e mainstream conference. It's held yearly in Springfield Mass and

is excellent - and affordable! There are scholarships available usually

for first-time parents to the conference. I think I cried the entire

time - it hit home! Luterman and Donna Sorkin were the two

keynote speakers and the " famous speaker " at the end of Day 2 was Curtis

Pride. What a story he has to tell! I remember just sobbing through

his whole talk thinking that surely my boys could also lead happy,

productive lives. It was so great so meet other Listen-up parents and

to get to talk to vendors - as a parent, we usually aren't able to do

that... I'm glad it was good for you!

Hugs,

Barbara

marabd wrote:

> I don't tend to write on the list, mostly lurk really, but my husband and

I

> went to the Conference (we just got back from our drive home) and I wanted

> to share a few thoughts. At the opening session, the teen group did a skit

> showing how they can do anything they want regardless of the hearing loss.

> It was full of funny lines but I sobbed through the whole thing. I was

just

> so touched by how well they were doing and how 'typical' and happy they

> were!

>

>

>

> I got to meet a mom whose name I've seen on the listserv and that was just

> wonderful. It was fun to connect with someone you feel like you know just

> b/c you've read your email! (Thanks Deganit).

>

>

>

> I loved learning about all the new technology - what is out now and what

is

> coming. My daughter is only 2 and already her hearing aids while good are

> not the newest hi-tech deal out there. I feel really optimistic about what

> the future in hearing aids holds (and CIs if she goes that route someday).

> Of course, I stuffed my bags with endless pens, cups, keychains, etc and

am

> now wondering why! You kind of get carried away in those exhibit halls.

>

>

>

> Finally, I learned so much. I went to some really good speakers -

> highlights for me were Carol Flexer's talks (I only knew to go hear her

b/c

> of this listserv) and one from Clinic's staff on play and

social

> interactions (tips on how to help our kids socially).

>

>

>

> It was very powerful being there surrounded by people who knew what I was

> feeling and going through as a mom. Professionals who cared enough to go

> into this field and to keep their knowledge current. And deaf and hard of

> hearing adults who were living their lives happily and successfully.

>

>

>

> On a totally different and very tragic note, I came home to really

horrible

> news. We are part of a family support group for parents of kids with HL.

> One of our moms and her two year old son died this weekend in a car

> accident. Life is so fleeting and I am so grateful for my family, friends,

> the parent group here in North Carolina, and all of you.

>

>

>

> Mara

>

> (mom of Ally, 2 yo, HA)

>

>

>

>

>

>

>

>

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In a message dated 6/28/2006 10:58:30 P.M. Central Standard Time,

marabd@... writes:

One of our moms and her two year old son died this weekend in a car

accident.

Oh how sad. :(

Putz

Illinois Families for Hands & Voices

_www.handsandvoices.org_ (http://www.handsandvoices.org/)

_www.ilhandsandvoices.org_ (http://www.ilhandsandvoices.org/)

Email: support@...

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I wonder if that is the funeral Pat Roush is attending later today. So

sad! We are going to see one of the other audiologists today for Sydney's

fitting . . . maaaaaaaaaybe . . . they don't think the molds are in. We're

sitting on standby this very minute . . . waiting for another call. I sure

wish Chapel Hill was closer.

>

> Mara - I'm so sorry to hear about the loss of the mom and child in your

>

> group - how awful!

>

> I'm so glad you got to go to AG Bell! I remember going to our first

> e mainstream conference. It's held yearly in Springfield Mass and

> is excellent - and affordable! There are scholarships available usually

> for first-time parents to the conference. I think I cried the entire

> time - it hit home! Luterman and Donna Sorkin were the two

> keynote speakers and the " famous speaker " at the end of Day 2 was Curtis

> Pride. What a story he has to tell! I remember just sobbing through

> his whole talk thinking that surely my boys could also lead happy,

> productive lives. It was so great so meet other Listen-up parents and

> to get to talk to vendors - as a parent, we usually aren't able to do

> that... I'm glad it was good for you!

>

> Hugs,

> Barbara

>

> marabd wrote:

> > I don't tend to write on the list, mostly lurk really, but my husband

> and I

> > went to the Conference (we just got back from our drive home) and I

> wanted

> > to share a few thoughts. At the opening session, the teen group did a

> skit

> > showing how they can do anything they want regardless of the hearing

> loss.

> > It was full of funny lines but I sobbed through the whole thing. I was

> just

> > so touched by how well they were doing and how 'typical' and happy they

> > were!

> >

> >

> >

> > I got to meet a mom whose name I've seen on the listserv and that was

> just

> > wonderful. It was fun to connect with someone you feel like you know

> just

> > b/c you've read your email! (Thanks Deganit).

> >

> >

> >

> > I loved learning about all the new technology - what is out now and what

> is

> > coming. My daughter is only 2 and already her hearing aids while good

> are

> > not the newest hi-tech deal out there. I feel really optimistic about

> what

> > the future in hearing aids holds (and CIs if she goes that route

> someday).

> > Of course, I stuffed my bags with endless pens, cups, keychains, etc and

> am

> > now wondering why! You kind of get carried away in those exhibit halls.

> >

> >

> >

> > Finally, I learned so much. I went to some really good speakers -

> > highlights for me were Carol Flexer's talks (I only knew to go hear her

> b/c

> > of this listserv) and one from Clinic's staff on play and

> social

> > interactions (tips on how to help our kids socially).

> >

> >

> >

> > It was very powerful being there surrounded by people who knew what I

> was

> > feeling and going through as a mom. Professionals who cared enough to go

> > into this field and to keep their knowledge current. And deaf and hard

> of

> > hearing adults who were living their lives happily and successfully.

> >

> >

> >

> > On a totally different and very tragic note, I came home to really

> horrible

> > news. We are part of a family support group for parents of kids with HL.

> > One of our moms and her two year old son died this weekend in a car

> > accident. Life is so fleeting and I am so grateful for my family,

> friends,

> > the parent group here in North Carolina, and all of you.

> >

> >

> >

> > Mara

> >

> > (mom of Ally, 2 yo, HA)

> >

> >

> >

> >

> >

> >

> >

> >

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>

> I live in Durham, NC and yes, we attend the Hitch-up (Hearing impaired

> children and teens have unlimited potential) group that meets in

Raleigh.

>>>>>

I live in Raleigh but have never went to the meeting. Jake is 12 now.

We used Pat when she was at Duke but we left and went to UNC for the CI

eval because Duke was not cooperating with us. We use Dr. Pillsbury

and the CCCDP CI program audiologists.

Do many older kids parents come to the meetings?

I will be thinking of you in this time of sadness.

Hugs,

Elaine

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Guest guest

I to went to the conference. The amount of info I learned was amazing, I am so

glad I went. I ended up purchasing the dry and store. The only thing that I

would change was that I arrived on Sat night (eventually after long delays) and

missed all the opening meet and greets. Though I had some conversations I feel

that I would have liked to meet some more parents.

Re: AG Bell conference feelings

I wonder if that is the funeral Pat Roush is attending later today. So

sad! We are going to see one of the other audiologists today for Sydney's

fitting . . . maaaaaaaaaybe . . . they don't think the molds are in. We're

sitting on standby this very minute . . . waiting for another call. I sure

wish Chapel Hill was closer.

>

> Mara - I'm so sorry to hear about the loss of the mom and child in your

>

> group - how awful!

>

> I'm so glad you got to go to AG Bell! I remember going to our first

> e mainstream conference. It's held yearly in Springfield Mass and

> is excellent - and affordable! There are scholarships available usually

> for first-time parents to the conference. I think I cried the entire

> time - it hit home! Luterman and Donna Sorkin were the two

> keynote speakers and the " famous speaker " at the end of Day 2 was Curtis

> Pride. What a story he has to tell! I remember just sobbing through

> his whole talk thinking that surely my boys could also lead happy,

> productive lives. It was so great so meet other Listen-up parents and

> to get to talk to vendors - as a parent, we usually aren't able to do

> that... I'm glad it was good for you!

>

> Hugs,

> Barbara

>

> marabd wrote:

> > I don't tend to write on the list, mostly lurk really, but my husband

> and I

> > went to the Conference (we just got back from our drive home) and I

> wanted

> > to share a few thoughts. At the opening session, the teen group did a

> skit

> > showing how they can do anything they want regardless of the hearing

> loss.

> > It was full of funny lines but I sobbed through the whole thing. I was

> just

> > so touched by how well they were doing and how 'typical' and happy they

> > were!

> >

> >

> >

> > I got to meet a mom whose name I've seen on the listserv and that was

> just

> > wonderful. It was fun to connect with someone you feel like you know

> just

> > b/c you've read your email! (Thanks Deganit).

> >

> >

> >

> > I loved learning about all the new technology - what is out now and what

> is

> > coming. My daughter is only 2 and already her hearing aids while good

> are

> > not the newest hi-tech deal out there. I feel really optimistic about

> what

> > the future in hearing aids holds (and CIs if she goes that route

> someday).

> > Of course, I stuffed my bags with endless pens, cups, keychains, etc and

> am

> > now wondering why! You kind of get carried away in those exhibit halls.

> >

> >

> >

> > Finally, I learned so much. I went to some really good speakers -

> > highlights for me were Carol Flexer's talks (I only knew to go hear her

> b/c

> > of this listserv) and one from Clinic's staff on play and

> social

> > interactions (tips on how to help our kids socially).

> >

> >

> >

> > It was very powerful being there surrounded by people who knew what I

> was

> > feeling and going through as a mom. Professionals who cared enough to go

> > into this field and to keep their knowledge current. And deaf and hard

> of

> > hearing adults who were living their lives happily and successfully.

> >

> >

> >

> > On a totally different and very tragic note, I came home to really

> horrible

> > news. We are part of a family support group for parents of kids with HL.

> > One of our moms and her two year old son died this weekend in a car

> > accident. Life is so fleeting and I am so grateful for my family,

> friends,

> > the parent group here in North Carolina, and all of you.

> >

> >

> >

> > Mara

> >

> > (mom of Ally, 2 yo, HA)

> >

> >

> >

> >

> >

> >

> >

> >

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Guest guest

We go to Dr. Buchman and Pat at UNC and are part of CCCDP, too. We are now

getting aids in July because the molds did not come in yet, just the aids.

We did have our appt. with Dr. Buchman today. He does NOT feel that Sydney

has LVAS. We are going to get an MRI now in August which will help us more

with that diagnosis. What I said WAS correct. You need the MRI to see if

the endolymphatic sacs are large, too.

RT in NC

>

>

> >

> > I live in Durham, NC and yes, we attend the Hitch-up (Hearing impaired

> > children and teens have unlimited potential) group that meets in

> Raleigh.

> >>>>>

>

> I live in Raleigh but have never went to the meeting. Jake is 12 now.

> We used Pat when she was at Duke but we left and went to UNC for the CI

> eval because Duke was not cooperating with us. We use Dr. Pillsbury

> and the CCCDP CI program audiologists.

>

> Do many older kids parents come to the meetings?

> I will be thinking of you in this time of sadness.

> Hugs,

> Elaine

>

>

>

--

Robin Tomlinson

thetomlinsons@...

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I thought the conference was great. I also took so many samples and

trinkets that they are floating around my living room in droves...of course,

with 4 kids, I had to get at least 4 of everything! (What am I going to do

with 5 oticon carrying cases???)

The best part, aside form (I wanted to hug that man, cried

through most of his session...) and Carol Flexer (2nd time I heard her) was

going to the exhibit hall and actually talking to the people who design this

equipment.. I talked someone's ear off at the Oticon place, and they

explained all about the trouble I am having with the new high frequency open

fit earlmold...looks like I am going back to the audi for a different kind

of fitting since Bobby's ear was bleeding last week, but now at least I

understand why after talking to the Oticon people. Talked the ear off of

the Phonak people who make our FM. Learned what cued speech is, talked to

all the schools in my area, got hooked up with a support group in NY which

is close to our house becasue the CT chapter isn't active any more, and I

just asked so many questions of so many people who actually knew all the

answers. It was wonderful!

Anyone know where it will be in 2008?

Well worth the 8 hr drive, though I missed the kids terribly.

Trish (mom to 4, one of which is 6 yrs old with newly diagnosed mod/severe

loss in one ear and high frequency loss in the other from ototoxic meds

given in ICU after one of his 4 open heart surgeries.

I to went to the conference. The amount of info I learned was amazing, I am

so glad I went. I ended up purchasing the dry and store. The only thing that

I would change was that I arrived on Sat night (eventually after long

delays) and missed all the opening meet and greets. Though I had some

conversations I feel that I would have liked to meet some more parents.

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Isn't wonderful? What a story he has to tell! I've heard

him speak at e School mainstream conference before - very moving...

Barbara

Trish Whitehouse wrote:

> The best part, aside form (I wanted to hug that man, cried

> through most of his session...)

>

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Trish,

Why was Bobby's ear bleeding? We have had problems with Elias's ear

bleeding - one incident caused quite a stir when the NP at Memorial

Sloan-Kettering

saw it. They had an ENT in Elias's room within the hour. Elias has

traditional

earmolds, though.

Also, where is the NY support group located?

Bonnie

>

> I thought the conference was great. I also took so many samples and

> trinkets that they are floating around my living room in droves...of

> course,

> with 4 kids, I had to get at least 4 of everything! (What am I going to do

>

> with 5 oticon carrying cases???)

>

> The best part, aside form (I wanted to hug that man, cried

> through most of his session...) and Carol Flexer (2nd time I heard her)

> was

> going to the exhibit hall and actually talking to the people who design

> this

> equipment.. I talked someone's ear off at the Oticon place, and they

> explained all about the trouble I am having with the new high frequency

> open

> fit earlmold...looks like I am going back to the audi for a different kind

>

> of fitting since Bobby's ear was bleeding last week, but now at least I

> understand why after talking to the Oticon people. Talked the ear off of

> the Phonak people who make our FM. Learned what cued speech is, talked to

> all the schools in my area, got hooked up with a support group in NY which

>

> is close to our house becasue the CT chapter isn't active any more, and I

> just asked so many questions of so many people who actually knew all the

> answers. It was wonderful!

>

> Anyone know where it will be in 2008?

>

> Well worth the 8 hr drive, though I missed the kids terribly.

>

> Trish (mom to 4, one of which is 6 yrs old with newly diagnosed mod/severe

>

> loss in one ear and high frequency loss in the other from ototoxic meds

> given in ICU after one of his 4 open heart surgeries.

>

> I to went to the conference. The amount of info I learned was amazing, I

> am

> so glad I went. I ended up purchasing the dry and store. The only thing

> that

> I would change was that I arrived on Sat night (eventually after long

> delays) and missed all the opening meet and greets. Though I had some

> conversations I feel that I would have liked to meet some more parents.

>

>

>

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In a message dated 6/30/2006 8:09:37 A.M. Eastern Daylight Time,

chester2001@... writes:

The support group in NY was in Westchester county, which is only about 45

minutes from me. They have a workshop for parents coming up in July if you

are interested, I have to register, it's for two days and looks like they

have a great speaker and time again to, network! (Did I mention how much

support I am FINALLY finding??)

Trish

Westchester? Where? Can I invite myself along in as well? Please share the

details, if you don't mind. Or send it off list. We're not in the new, early

stages but I am always looking to learn more and meet other parents.

And I am so glad you've found the support, it really does make a world of

difference!

Jill

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Bonnie,

It seems that these open ear molds (thin tubing that goes right into the ear

canal) were made for adults and these high frequency hearing aids have never

been used for kids until about a couple of months ago. So even though we

are using the smallest tubing, it is still probabbly too big for a little

kid's ear canal and when I put it in, it irritated his ear enough that it

started to bleed. I took him to the ped that day and he said that it was

superficial, just at the entrance of the canal, to leave the aid out a few

days and it would heal, which it did.

But what the Oticon rep suggested is that we have an impression of his ear

canal on that side made to see just how big, wide, long, etc it is, and then

have a custom ear mold made or at least we'll know if the size of the tubing

is the problem. Made sense to me, and then I had the luxury of walking

right across the exhibit hall and talking to his audiologist from

Soundbridge about the problem, so they'll take care of it from there. (The

networking there was incredible.)

The support group in NY was in Westchester county, which is only about 45

minutes from me. They have a workshop for parents coming up in July if you

are interested, I have to register, it's for two days and looks like they

have a great speaker and time again to, network! (Did I mention how much

support I am FINALLY finding??)

Trish

Trish,

Why was Bobby's ear bleeding? We have had problems with Elias's ear

bleeding - one incident caused quite a stir when the NP at Memorial

Sloan-Kettering

saw it. They had an ENT in Elias's room within the hour. Elias has

traditional

earmolds, though.

Also, where is the NY support group located?

Bonnie

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Guest guest

I live in Westchester County, so I definitely am interested. Could you send

me

the info?

The MSKCC ENT determined that the bleeding from Elias's ear was also due

to a superficial wound to the entrance of the canal, probablly from the

earmolds

(but no one knows for sure). He was on a 3F8 round at the time, so they

had to take any weird symptom seriously. Since then, he has had blisters

in his ear, where the helix lock is. When he had his new earmolds done, the

audiologist tried to use a smaller helix lock, but I am not convinced that

it

helps.

Bonnie

>

> Bonnie,

>

> It seems that these open ear molds (thin tubing that goes right into the

> ear

> canal) were made for adults and these high frequency hearing aids have

> never

> been used for kids until about a couple of months ago. So even though we

> are using the smallest tubing, it is still probabbly too big for a little

> kid's ear canal and when I put it in, it irritated his ear enough that it

> started to bleed. I took him to the ped that day and he said that it was

> superficial, just at the entrance of the canal, to leave the aid out a few

>

> days and it would heal, which it did.

>

> But what the Oticon rep suggested is that we have an impression of his ear

>

> canal on that side made to see just how big, wide, long, etc it is, and

> then

> have a custom ear mold made or at least we'll know if the size of the

> tubing

> is the problem. Made sense to me, and then I had the luxury of walking

> right across the exhibit hall and talking to his audiologist from

> Soundbridge about the problem, so they'll take care of it from there. (The

>

> networking there was incredible.)

>

> The support group in NY was in Westchester county, which is only about 45

> minutes from me. They have a workshop for parents coming up in July if you

>

> are interested, I have to register, it's for two days and looks like they

> have a great speaker and time again to, network! (Did I mention how much

> support I am FINALLY finding??)

>

> Trish

>

>

>

>

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Guest guest

Trish, we are having the same problem with Maggie and she is almost 15! We are

trialing the Phonak MicroPower and the " dome " is too darn big! They only have

two sizes and this is the smallest one. In the Sebotek aid she used the next to

the smallest dome. So we are forging ahead.

It seems that these open ear molds (thin tubing that goes right into the ear

canal) were made for adults and these high frequency hearing aids have never

been used for kids until about a couple of months ago. So even though we

are using the smallest tubing, it is still probabbly too big for a little

kid's ear canal and when I put it in, it irritated his ear enough that it

started to bleed. I took him to the ped that day and he said that it was

superficial, just at the entrance of the canal, to leave the aid out a few

days and it would heal, which it did.

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I have to look through a ton of papers and information I got at the

conference, which I just started doing today anyway, so I'll post this info

later today.

Trish

Re: AG Bell conference feelings

In a message dated 6/30/2006 8:09:37 A.M. Eastern Daylight Time,

chester2001@... writes:

The support group in NY was in Westchester county, which is only about 45

minutes from me. They have a workshop for parents coming up in July if you

are interested, I have to register, it's for two days and looks like they

have a great speaker and time again to, network! (Did I mention how much

support I am FINALLY finding??)

Trish

Westchester? Where? Can I invite myself along in as well? Please share the

details, if you don't mind. Or send it off list. We're not in the new, early

stages but I am always looking to learn more and meet other parents.

And I am so glad you've found the support, it really does make a world of

difference!

Jill

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Hi, there, Mara!

I've been dilinquent in reading posts because of so much post-

conference stuff to do since Tuesday, but it was so great to meet

you and trade stories. Don't you love that 6-sound song book? Jordan

loves it and keeps requesting that I sing it with her.

I had the same feelings throughout the conference and felt

profoundly sad when it was time to leave and enter back into

the " real " world (except I missed my family dearly)...

I'm so sorry to hear about the loss of the mother and child that you

knew - how terrible and tragic.

Was great to meet you,

Deganit

>

> >

>

> I got to meet a mom whose name I've seen on the listserv and that

was just

> wonderful. It was fun to connect with someone you feel like you

know just

> b/c you've read your email! (Thanks Deganit).

>

>

>

> >

>

>

>

>

>

>

>

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