Welcome, Laura!
Kathy Jo Pink
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Pogo Nickname : perkypinkypink
> Date: Mon, 13 Sep 2010 09:13:56 -0700
> From: [log in to unmask]
> To: [log in to unmask]
>
> Thanks Kathy! I am excited to find a real group, ha, ha. I have been looking
> for awhile and have been very frustrated by the number of attorney firms that
> pose as CP support groups. Let me introduce myself to everyone. My name is
> Laura and I am a mom to 4 wonderful kids. My youngest son, Seth (14 months old
> now) was born 16 weeks early at a whole whopping 1 lb 7 oz. Due to his extreme
> prematurity he had several medical problems at birth including Intraventricular
> hemorrhage (brain bleeds) grade 3 and grade 4 with resulting hydrocephalus.
> Three weeks ago he was diagnosed with CP. He has low muscle tone in his neck,
> upper torso and lower extremeties with spasms below the knees, although no
> contractures. While I knew from the time he was born that getting a diagnosis
> of CP was a very real possibility, having it actually said has made me an
> emotional train wreck. Adding to that, just trying to take all the new
> information in, acquiring equipment, starting new therapies is it's own
> challenge. I got divorced while my son was still in the NICU so there's nobody
> for me to talk to about worries and concerns. It's even more frustrating for me
> at times because I've been a nurse for several years now, but have no experience
> in this area. There's so much information, some very conflicting, to sort
> through.
>
>
> Wow, that sounds like I'm ranting doesn't it?! I am excited to get to know
> everyone, and I hope nobody minds me picking your brains for information. And
> maybe letting me vent once in awhile. I promise not to make it a habit, lol.
> It really is kind of a relief just knowing there's others out there that are
> affected by the same thing, in some way, and joining together to support one
> another.
>
>
> I look forward to talking with you all more.
>
> Laura
>
>
>
>
>
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