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Hello everyone,

My name is and my son , age 3, was recently diagnosed with mild to

moderate bilateral hearing loss. He failed the newborn screening at birth in

2002 and was referred to a different hospital for further testing. The results

at that time showed an extremely mild loss in one ear and nothing further was

recommended as long as he continued to meet all developmental milestones...I

shouldn't have listened to them. He met all milestones on time but his speech

did not develop as I thought it should and I mentioned this many, many times to

his pediatrician but was told I was worrying for nothing.

Over the summer I noticed, he began to watch my mouth when I talked and began to

repeatedly ask " what did you say " . We took him to a pediatric ENT in September

who confirmed the loss. He got hearing aids in early October and just started 2

mornings a week at the classes offered for hearing impaired children through our

local school district. We were very fortunate to have found an incredible

pediatric audiologist/hearing aid dispenser who has been an invaluable resource

to us! is adjusting to all the changes very well - I'm so proud of him!

I'm glad to have found this group and hope that you will be able to answer more

of my questions as they come up!

S. in Tennessee

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Hi - welcome! I have two boys who now are 13 and 11. Tom just

had cochlear implant surgery (about 3 weeks ago) but did wear two

hearing aids up until then; Sam is my 11 year old, is profoundly deaf

and wears hearing aids. I'm so glad you've found such good supports

already!

Barbara

blueroos@... wrote:

> Hello everyone,

>

> My name is and my son , age 3, was recently diagnosed

> with mild to moderate bilateral hearing loss. He failed the newborn

> screening at birth in 2002 and was referred to a different hospital

> for further testing. The results at that time showed an extremely mild

> loss in one ear and nothing further was recommended as long as he

> continued to meet all developmental milestones...I shouldn't have

> listened to them. He met all milestones on time but his speech did

> not develop as I thought it should and I mentioned this many, many

> times to his pediatrician but was told I was worrying for nothing.

>

> Over the summer I noticed, he began to watch my mouth when I talked

> and began to repeatedly ask " what did you say " . We took him to a

> pediatric ENT in September who confirmed the loss. He got hearing

> aids in early October and just started 2 mornings a week at the

> classes offered for hearing impaired children through our local school

> district. We were very fortunate to have found an incredible

> pediatric audiologist/hearing aid dispenser who has been an invaluable

> resource to us! is adjusting to all the changes very well -

> I'm so proud of him!

>

> I'm glad to have found this group and hope that you will be able to

> answer more of my questions as they come up!

>

> S. in Tennessee

>

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,

I apologize, but I think I missed your post. Welcome to the group!

There are quite a few parents here whose kids were identified at their

newborn screening and have experience with the Early Intervention programs. they

certainly have experience with everything from getting aids into little ones

and keeping them there. (grin) So I am sure you're going to find plenty of

people to share their experience and wisdom.

Ask any questions that come to mind. I'm sure someone here has an idea to

address it. We've discussed everything from potty training to identifying

mysterious rashes (turned out to be a yeast infection) to how to deal with our

less than supportive families.

Our Ian was about 7½ when we first learned of his hearing loss --the end of

2nd grade. It wasn't until 4th grade that he was aided. A collection of bad

doctors and misinformation made the process more difficult than it needed to

be.

Since Ian was so much older, I have no experience with little ones and

hearing loss, but there are so many people here who do. I know you'll find

answers

and if we don't have any, we know how to find them!

Best -- Jill

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Hi ,

It's nice to " meet " you. I'm Debbie, mom to two very active kids,

and . is 6 and has a moderate bilateral SNHL. is 3 and

although he can hear....he never listens.

wasn't diagnosed until she was 2 1/2. We missed the newborn

screenings at our hospital by six months. We didn't discover her loss until she

was 2 1/2. Like you our ped wasn't concerned about her lack of speech

development. She had maybe 10 words at 2 years that we could understand. He

reasured us that all kids progress at different rates. Eventually I had her

screened by our states EI program, for her speech delay. After being in therapy

for a month our EI coordinator suggested a hearing test. The rest is history.

is currently in first grade at our neighborhood school. She is

outgoing and down right silly most days. Her favorite things to do are to draw

and dance, and she's quite good at both (not that I'm biased or anything ;o)

Debbie

Some men see things as they are and ask why. Others dream things that never were

and ask why not. G.B Shaw

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

Yahoo! Shopping

Find Great Deals on Holiday Gifts at Yahoo! Shopping

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  • 2 years later...
Guest guest

I too am a medical transcriptionist. I also do speech recognition editing

(I love it and it isn't as hard on my fibro!). Good to meet you!

Tabi D

<:))))><

_____

From: Fibromyalgia_Support_Group

[mailto:Fibromyalgia_Support_Group ] On Behalf Of Jana Metz

Sent: Monday, March 03, 2008 8:10 PM

To: Fibromyalgia_Support_Group

Subject: Re: new member intro

Hi Tabi,

I like your name!! I also am able to work at home--part time and at the

office 2 days a week. What type of work do you do? I am a medical

transcriptionist. I, like you, couldn't imagine going into the office every

day. I work Mondays and Wednesdays at the office. I don't have too much of a

problem on Wednesdays, because Thursday is my day off and I am looking

forward to that----but Mondays is very hard for me to get motivated to get

into the office. My boss is sympathetic to my situation and is happy for me

to work at home, so I can keep working, but one of my coworkers doesn't

understand and I think she is thinking that I get preferential treatement.

Anyway, just wanted to say hi!

Jana

Tabi D <tabimt (AT) embarqmail (DOT) <mailto:tabimt%40embarqmail.com> com> wrote:

Hey all. My name is Tabi. I am 33 years old, married with 3 kiddos. I

have fibro for at least 13 years now. ICK. I am going to ask my doc for

Lyrica tomorrow. I am already on Kadian (morphine sulfate). I work from

home, which is ideal for me. I don't think I could handle driving to an

office every day, dealing with people on a daily basis who have no idea what

I am going through, etc.

Well, am glad to be a part of this group. Have a great day!

Tabi D

<:))))><

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Guest guest

Tabi,

Welcome aboard. We look forward to getting to know you better! How

old are your kids? I have 2 grown children; am remarried and we

adopted a set of special needs twins last year. Was recently dx'd, am

on medical disability fighting for SSD. Glad you are able to work

from home; that is definitely a blessing for you! I don't know the

med you are currently taking; I have been on Lyrica since 1/18/08

(started 75 mg 2x a day, up to 150 mg 2x/day, seems to be working

although I notice I am having some flares lately and some break-thru

pain. But it's okay. I'm learning how to deal with it, one day at a

time!

Darlene

>

> Hey all. My name is Tabi. I am 33 years old, married with 3

kiddos. I

> have fibro for at least 13 years now. ICK. I am going to ask my

doc for

> Lyrica tomorrow. I am already on Kadian (morphine sulfate). I

work from

> home, which is ideal for me. I don't think I could handle driving

to an

> office every day, dealing with people on a daily basis who have no

idea what

> I am going through, etc.

>

> Well, am glad to be a part of this group. Have a great day!

>

> Tabi D

> <:))))><

>

>

>

>

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Guest guest

Thanks! I have 3 kiddos - ages 13, 9, and 8. they keep me on my toes, let

me tell ya!

Tabi D

<:))))><

_____

From: Fibromyalgia_Support_Group

[mailto:Fibromyalgia_Support_Group ] On Behalf Of ddean228

Sent: Tuesday, March 04, 2008 11:01 AM

To: Fibromyalgia_Support_Group

Subject: Re: new member intro

Tabi,

Welcome aboard. We look forward to getting to know you better! How

old are your kids? I have 2 grown children; am remarried and we

adopted a set of special needs twins last year. Was recently dx'd, am

on medical disability fighting for SSD. Glad you are able to work

from home; that is definitely a blessing for you! I don't know the

med you are currently taking; I have been on Lyrica since 1/18/08

(started 75 mg 2x a day, up to 150 mg 2x/day, seems to be working

although I notice I am having some flares lately and some break-thru

pain. But it's okay. I'm learning how to deal with it, one day at a

time!

Darlene

>

> Hey all. My name is Tabi. I am 33 years old, married with 3

kiddos. I

> have fibro for at least 13 years now. ICK. I am going to ask my

doc for

> Lyrica tomorrow. I am already on Kadian (morphine sulfate). I

work from

> home, which is ideal for me. I don't think I could handle driving

to an

> office every day, dealing with people on a daily basis who have no

idea what

> I am going through, etc.

>

> Well, am glad to be a part of this group. Have a great day!

>

> Tabi D

> <:))))><

>

>

>

>

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Guest guest

Thanks! I have 3 kiddos - ages 13, 9, and 8. they keep me on my toes, let

me tell ya!

Tabi D

<:))))><

_____

From: Fibromyalgia_Support_Group

[mailto:Fibromyalgia_Support_Group ] On Behalf Of ddean228

Sent: Tuesday, March 04, 2008 11:01 AM

To: Fibromyalgia_Support_Group

Subject: Re: new member intro

Tabi,

Welcome aboard. We look forward to getting to know you better! How

old are your kids? I have 2 grown children; am remarried and we

adopted a set of special needs twins last year. Was recently dx'd, am

on medical disability fighting for SSD. Glad you are able to work

from home; that is definitely a blessing for you! I don't know the

med you are currently taking; I have been on Lyrica since 1/18/08

(started 75 mg 2x a day, up to 150 mg 2x/day, seems to be working

although I notice I am having some flares lately and some break-thru

pain. But it's okay. I'm learning how to deal with it, one day at a

time!

Darlene

>

> Hey all. My name is Tabi. I am 33 years old, married with 3

kiddos. I

> have fibro for at least 13 years now. ICK. I am going to ask my

doc for

> Lyrica tomorrow. I am already on Kadian (morphine sulfate). I

work from

> home, which is ideal for me. I don't think I could handle driving

to an

> office every day, dealing with people on a daily basis who have no

idea what

> I am going through, etc.

>

> Well, am glad to be a part of this group. Have a great day!

>

> Tabi D

> <:))))><

>

>

>

>

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Guest guest

Thanks! I have 3 kiddos - ages 13, 9, and 8. they keep me on my toes, let

me tell ya!

Tabi D

<:))))><

_____

From: Fibromyalgia_Support_Group

[mailto:Fibromyalgia_Support_Group ] On Behalf Of ddean228

Sent: Tuesday, March 04, 2008 11:01 AM

To: Fibromyalgia_Support_Group

Subject: Re: new member intro

Tabi,

Welcome aboard. We look forward to getting to know you better! How

old are your kids? I have 2 grown children; am remarried and we

adopted a set of special needs twins last year. Was recently dx'd, am

on medical disability fighting for SSD. Glad you are able to work

from home; that is definitely a blessing for you! I don't know the

med you are currently taking; I have been on Lyrica since 1/18/08

(started 75 mg 2x a day, up to 150 mg 2x/day, seems to be working

although I notice I am having some flares lately and some break-thru

pain. But it's okay. I'm learning how to deal with it, one day at a

time!

Darlene

>

> Hey all. My name is Tabi. I am 33 years old, married with 3

kiddos. I

> have fibro for at least 13 years now. ICK. I am going to ask my

doc for

> Lyrica tomorrow. I am already on Kadian (morphine sulfate). I

work from

> home, which is ideal for me. I don't think I could handle driving

to an

> office every day, dealing with people on a daily basis who have no

idea what

> I am going through, etc.

>

> Well, am glad to be a part of this group. Have a great day!

>

> Tabi D

> <:))))><

>

>

>

>

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  • 5 months later...



Hello Sharon ... a quick welcome to our group. You have been through so much and you will be glad you are here. Always someone with an answer and/or support.

I swallowed the radioactive iodine back in the late 70s for a thyroid goiter as well.

I've had "yes" and I've had "no" answers as to it being a cause of my IPF --- switched to NSIP.

We're in 3 digit heat here in Oregon and I'm too pooped to type. I'll watch for your posts.

BTW, my given name is Sharon as well. Great name!

MamaSher, age 70. IPF 3-06, OR. NasturtiumsDon't fret about tomorrow, God is already there!

New member intro

Hi all,

I'm Sharon, 33yr old mother of 3 from Australia. I'm currently 13mths away from graduating university as a registered nurse and three days ago I was told I have fibrosis & areas of collaspe.

My story starts May 07, with my first episode of crackles, shortness of breath. The hospital put it down to an acute asthma attack (first ever) and treated me with nebs & after a few hours I went home ok. As the months progressed I had the occasional repeat episode which only came on after a specific exercise. Fast forward to the end of 07 and I was now waking at night with these episodes and they were lasting up to 12hours. In December 07 I had a CTPA (ct scan with contrast dye to check for pulmonary embolisms) they concuded the ground glass appearance at the bases was due to broncho pneumonia & treated for such.

Since then I have had more and more episodes and gradual worsening. After a wisdom tooth extraction on friday I had another, what I called "Mild" episode but at least my local doctor was open so I went to him (most other attacks were at night or when he was shut) so he could see for himself what was happening. He sent me straight to the hospital, who after keeping me for several hours sent me home with instructions for my local doctor to refer me to a lung specialist & arrange a high resolution CT. After I left the local doctor my dad was next to see him about his own health issue, the doctor said to my dad that he thought it was just an anxiety attack from the tooth extraction.

My high res CT stated I have bilateral pulmonary effusions, areas of collaspe in the middle lobe & lingular, septal thickening in the middle lobe & ground glass or air trapping in the bases. To which my local doctor said "YOU HAVE FIBROSIS & AREAS OF COLLASPE" and then wrote me a referral to a lung specialist. We've had a few public holidays here so I'm waiting until Tuesday next week to chase up the appointment but I left my local doctor with no guidence, medication or instructions aside from "JUST WAIT" till I get the appointment.

I have never smoked but both my parents smoked heavily all my life, my mother has passed away so I moved in with dad 2yrs ago to help him and moved back into the smoke environment. I'm numb, trying not to freak out and if I didn't have false nails I would have bitten my nails down to the knuckle.

I know there are various types of fibrosis and considering I have had radiation treatment (radioactive iodine 15yrs ago) for thyroid disease that puts me at a high "risk" category for some types. But I'm still hoping that my local doctor has made an grasping at sraws diagnosis, and know that I will know more when I see the specialist.

Just wanted to blurt my "story" out and say hi.

take care

Sharon.

Win a MacBook Air or iPod touch with Yahoo!7- Find out more.

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Hi Sharon, I have PF. I'm two years older than you. Welcome to the group, you'll find a lot of support/answers here! IrenePF 03/07 Raynaud's Disease 09/07

New member intro

Hi all,

I'm Sharon, 33yr old mother of 3 from Australia. I'm currently 13mths away from graduating university as a registered nurse and three days ago I was told I have fibrosis & areas of collaspe.

My story starts May 07, with my first episode of crackles, shortness of breath. The hospital put it down to an acute asthma attack (first ever) and treated me with nebs & after a few hours I went home ok. As the months progressed I had the occasional repeat episode which only came on after a specific exercise. Fast forward to the end of 07 and I was now waking at night with these episodes and they were lasting up to 12hours. In December 07 I had a CTPA (ct scan with contrast dye to check for pulmonary embolisms) they concuded the ground glass appearance at the bases was due to broncho pneumonia & treated for such.

Since then I have had more and more episodes and gradual worsening. After a wisdom tooth extraction on friday I had another, what I called "Mild" episode but at least my local doctor was open so I went to him (most other attacks were at night or when he was shut) so he could see for himself what was happening. He sent me straight to the hospital, who after keeping me for several hours sent me home with instructions for my local doctor to refer me to a lung specialist & arrange a high resolution CT. After I left the local doctor my dad was next to see him about his own health issue, the doctor said to my dad that he thought it was just an anxiety attack from the tooth extraction.

My high res CT stated I have bilateral pulmonary effusions, areas of collaspe in the middle lobe & lingular, septal thickening in the middle lobe & ground glass or air trapping in the bases. To which my local doctor said "YOU HAVE FIBROSIS & AREAS OF COLLASPE" and then wrote me a referral to a lung specialist. We've had a few public holidays here so I'm waiting until Tuesday next week to chase up the appointment but I left my local doctor with no guidence, medication or instructions aside from "JUST WAIT" till I get the appointment.

I have never smoked but both my parents smoked heavily all my life, my mother has passed away so I moved in with dad 2yrs ago to help him and moved back into the smoke environment. I'm numb, trying not to freak out and if I didn't have false nails I would have bitten my nails down to the knuckle.

I know there are various types of fibrosis and considering I have had radiation treatment (radioactive iodine 15yrs ago) for thyroid disease that puts me at a high "risk" category for some types. But I'm still hoping that my local doctor has made an grasping at sraws diagnosis, and know that I will know more when I see the specialist.

Just wanted to blurt my "story" out and say hi.

take care

Sharon.

Win a MacBook Air or iPod touch with Yahoo!7- Find out more.

Be smarter than spam. See how smart SpamGuard is at giving junk email the boot with the All-new Yahoo! Mail

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