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In a message dated 9/22/2000 9:07:21 AM Eastern Daylight Time,

indrel@... writes:

<< Wish me luck! >>

Good Luck to you!!!!!!!!

Cathy Morrow in Lenoir, NC

BMI 42

A journey of a thousand miles begins with a single step

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This is my first post! I have been researching my options for

approx. 6 months now. I'm so happy that I found Dr. R's web site.

Amy Poe's story really inspired me. It's nice to know there is hope.

I am 36 with 3 sons, 1 husband and a full time demanding job. I have

been searching for something that would provide a fast recovery. Mini

shounds like my answer to prayers. I am just starting this journey

and am currently getting my paper work together to send to Dr. R. Any

insite would be helpful at this point. My current BMI is 42. My

insurance plan book says that any treatment for Morbid Obesity will

be covered. They define MO as being 100# over weight. If thats all

they need I should have no problem. It scares me to read all of the

problems everyone else is having with their insurance. Wish me luck!

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  • 3 years later...

In a message dated 10/6/2003 7:30:58 AM Central Daylight Time,

karonrbetz@... writes:

KaronB

Welcome this is a great group to join!! I am a mom of three daughters and two

of them have CF. You will learn a lot here from this group. So if you have

any question you have come to the right place. Deb A

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Hi Karon,

Welcome to our list. You'll find lots of support,

information and optimism here. I'm glad that your

son was diagnosed at birth. It makes all the

difference in the world.

Best wishes,

C

Mommy to Mick and Alli, 3.5 yo twins wcf

--- Karon Betz wrote:

> Hello Everyone.

>

> I just found this group tonight and wanted to

> introduce myself. I am the

> mother of an 11 month old boy with CF. He was pretty

> much diagnosed at birth

> when they performed emergency surgery for meconium

> ileus. He was less than

> 36 hours old and still 4 weeks early. But he made it

> through like a trooper.

> They started him on albuterol treatments after he

> came off the respirator

> (from surgery-not from being premie) and enzymes as

> soon as he was drinking

> milk.

> He's now doing great. Most people who meet him are

> shocked when we say he

> has CF. He is scheduled for his second set of PFT's

> this Friday. It should

> be interesting to see how he handles them. The

> biggest challenge the first

> time was keeping him awake on the drive in - of

> course we got stuck in rush

> hour traffic!

> Anyway, I am excited to share ideas, challenges

> and most of all

> accomplishments with all of you.

>

> Regards,

> KaronB

>

>

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,

Welcome to our group. Good luck with the PFT's.

Tina W., mother of , almost 18yoa wcf

Hello!

Hello Everyone.

I just found this group tonight and wanted to introduce myself. I am the

mother of an 11 month old boy with CF. He was pretty much diagnosed at birth

when they performed emergency surgery for meconium ileus. He was less than

36 hours old and still 4 weeks early. But he made it through like a trooper.

They started him on albuterol treatments after he came off the respirator

(from surgery-not from being premie) and enzymes as soon as he was drinking

milk.

He's now doing great. Most people who meet him are shocked when we say he

has CF. He is scheduled for his second set of PFT's this Friday. It should

be interesting to see how he handles them. The biggest challenge the first

time was keeping him awake on the drive in - of course we got stuck in rush

hour traffic!

Anyway, I am excited to share ideas, challenges and most of all

accomplishments with all of you.

Regards,

KaronB

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Welcome to the group!

,

mom of , 5 on friday with CF

Hello!

Hello Everyone.

I just found this group tonight and wanted to introduce myself. I am the

mother of an 11 month old boy with CF. He was pretty much diagnosed at birth

when they performed emergency surgery for meconium ileus. He was less than

36 hours old and still 4 weeks early. But he made it through like a trooper.

They started him on albuterol treatments after he came off the respirator

(from surgery-not from being premie) and enzymes as soon as he was drinking

milk.

He's now doing great. Most people who meet him are shocked when we say he

has CF. He is scheduled for his second set of PFT's this Friday. It should

be interesting to see how he handles them. The biggest challenge the first

time was keeping him awake on the drive in - of course we got stuck in rush

hour traffic!

Anyway, I am excited to share ideas, challenges and most of all

accomplishments with all of you.

Regards,

KaronB

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