I can still do it! We can figure something out. Be thinking of a style.
I can still do it! We can figure something out. Be thinking of a style.
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
kim is a hair stylist, so I can ask her to help you with your hair for the ball. I am sure she won't mind. Aunt Nancy
Aunt Nancy--GREAT TO HEAR FROM YOU!!!
What fun we will have getting ready for the ball!!!!!!!
Two hair stylists now!
Were all going to look beautiful.
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]
Steph, I have seen your pic, you are beautiful already!
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
I need help with my hair too . I have gone from long and curly to short and straight. You guys would die if you saw how much I paid to get my hair done. I have just started going to someone new (twice now) and haven't just gotten a cut (highlights and cut the first time, and roots the second time) but I was tired of my old stylist just doing the same thing just longer/shorter layers. I needed a knew, bolder look and this gal wasn't afraid to go for it. Jeff loves it and doesn't ask. He too will get me the occasional spa package which is really nice. I used it on my hair last time, I still have a credit so I am thinking of that massage!
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
My Jeff hates it when I get a cut because he likes long hair. I have grown it for him several times but it is too much work and looks stringy! When it starts to grow on his head then he can wear it the way he wants to! Show us a pic of the new 'do Tara!
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
LOL I am in the middle of straightening it right now. Only thing about this do is it takes forever. I am not kidding from drying to finish it is about an hour! My hair is naturally wavy so it is a pain but I do like it. When I get done I will have Brandon take a picture and I will try to figure out how to post it. We have VBS tonight so it might be later .
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 constantly change my hair style. I'm my hairdressers dream come true cause I walk in and tell her to change it up and have fun choosing what she thinks I'd be good with. I get hair bored sooooo easy and to be honest, I don't like it when gals have long hair and all they do is pull it back. DO SOMETHING WITH THAT HAIR! Oh and don't get me started on men dictating how hair shoudl be. That is one topic that highly upsets me - worse than flip flops upset me.
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.
Kara! Don't rip on people with long hair that pull it back! That's totally me I love long hair, but I have to pull it back for work and because I am lazy. Though I am a mom, I am not ready for a "mom" do.
I hate having hair that you have to do' that must be why I also don't wear makeup.
I will make sure that I wear my hair down everyday at hte conference.
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 won't take sides about the the hair but that is why I usually end up cutting mine because I just end up pulling it up in a pony tail and i wind up with a head ache. But i do love my flip flops too!
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