Dawn, you like a princess! I love them both!
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Dawn, you like a princess! I love them both!
cdh found at birth. 28 days NICU. Vent 7 days. Repair at 3 days. No ECMO. NG Tube 28 days http://i319.photobucket.com/albums/m...don/0004-1.jpg
Dawn-They both are beautiful!!!!!
I am wearing flip flops--just for you Kara!!! lol
Stephanie (Shelby's Mom LCDH 7-10-06)- ECMO 7 days- 2 DH repairs- hital hernia repair- Cliff Lip repair- Nissen and Mickey button. Shelby is eating and drinking by mouth now!!! THIS IS FANTASTIC!!!!! Mom to Lexi 8- Morgan 6 and Taylor 5. Blessed to have our little butterfly and our beautiful girls. [url]www.youtube.com/cdhsupport[/url] - Shelby's Journey [img]http://i258.photobucket.com/albums/hh257/gracebutterfly/CDHAwarenessRibbonShelbysmall.jpg[/img]
Oh Dawn-they are both beautiful! I really love the first one!!!
Corin New England State Rep [img]http://i171.photobucket.com/albums/u312/GabrielMommy1118/1-3.jpg[/img] [url]www.gabriel-nava.virtual-memorials.com[/url] Gabriels website [url]http://www.youtube.com/watch?v=N66S-vt5sI8[/url] Gabriels Video [url]http://corinscrazylife.blogspot.com/[/url] My Blog [url]http://newenglandcherubs.wordpress.com[/url] New England Blog
Dawn, I think the first one is the one for you for this ball. I really like the second one but for some reason I keep going back to the first one and I look at it and think that is what youo envisioned for this whole thing. It is really beautiful and I think you look fantastic in it.
Kara I love the shoes. Mine are a tad pointy. Jeff has told me to start practicing walking in them LOL
Mom to Brandon 7/17/96 LCDH repaired six times- ECMO seven days- nissen and g-tube at three weeks- g-tube removed at five years- slight scoliosis Also Co-Rep for the State of Ohio
I like both of them. I still need to buy shoes. I should go today, after I check all 421 messages on here! We had family visit and I haven't been on since wednesday or thursday! Geesh!
Amy Miles Faith Grace Miles Born 3-6-08- she lost her battle with CDH on 4-5-08 due to complications with deficiencies in blood clotting factors- albumin leakage from silo- pnuemothorax- and PPHN. LCDH- stomach- bowels- and liver/gallbladder up and gortex repair http://i304.photobucket.com/albums/n...Gracesmall.jpg www.carepages.com (search for FaithGraceCDH) www.firstgiving.com/faithgracecdh __________________________________________________ _____________ A gift from Heaven due on July 4th- 2009... http://bd.lilypie.com/pABbm5.png <a><img></a>
Thanks, ladies. Not sure if I'm going to be able to get the dress altered in time though. I've lost 8 lbs in the past 2 week - will probably lose another 5 before the events (stress is the best diet. lol) so it has to be taken in. I dropped it off at a tailor shop and they wanted to charge me twice as much as what I paid for the dress. Just to hem it straight across the bottom (no lace, nothing) was $75. Time to get out my old sewing machine I guess. I haven't even started looking for shoes yet. I think I'm just doing the ballet slipper thing so I don't trip and hurt someone. I am too clumsy for high heels.
Mom of Shane (1/28/93-9/11/99) LCDH x6 and multiple complications and birth defects.
Founder and President of CDH International.
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I think I am going to go for slippers or flip flops. i will have to stay away from Kara though
Amy Miles Faith Grace Miles Born 3-6-08- she lost her battle with CDH on 4-5-08 due to complications with deficiencies in blood clotting factors- albumin leakage from silo- pnuemothorax- and PPHN. LCDH- stomach- bowels- and liver/gallbladder up and gortex repair http://i304.photobucket.com/albums/n...Gracesmall.jpg www.carepages.com (search for FaithGraceCDH) www.firstgiving.com/faithgracecdh __________________________________________________ _____________ A gift from Heaven due on July 4th- 2009... http://bd.lilypie.com/pABbm5.png <a><img></a>
I'm speechless . . . . . .
Kara- mom to Aaron (8-30-03) and Adam- LCDH (8-7-06). Gastric Volvulus at 7 months old; Borderline Chiari Malformation; reherniation- bowel blockage and intestional malrotation at 26 months old; Apraxia of Speech - neurological speech disorder; Auditory Processing Disorder; Asthma; and frequent headaches.
I am thinking of flip flops too but i am just 5'1' so that may not be such a good idea. But at my age i have to be comfortable.
cdh found at birth. 28 days NICU. Vent 7 days. Repair at 3 days. No ECMO. NG Tube 28 days http://i319.photobucket.com/albums/m...don/0004-1.jpg
Dawn I found a seamstress on Craigslist. I am just praying that she does a good job and returns my dress. That would be my luck
Mom to Brandon 7/17/96 LCDH repaired six times- ECMO seven days- nissen and g-tube at three weeks- g-tube removed at five years- slight scoliosis Also Co-Rep for the State of Ohio
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