Sunday, January 25, 2009
Oh, what a glorious day!
Tuesday, January 20, 2009
A lot of Catching-up to do!

waiting for the ball to drop
HI-HO, HI-HO
not so preemie
Evidently preemie's that come back for the neonatal follow-up clinic at Aultman don't typically weigh 15 lbs at 5 1/2 months (3 months corrected age). Remember, she only weighed 2 lbs 14 1/2 oz at birth. My little lady is a chunk, correction CHUNK. I'm telling you, you would never know Audrey was a preemie. Maybe her weight has something to do with her three night time feedings....eek! Any advice here would be greatly appreciated. You can imagine being back at work and still getting up for three feedings a night! It's exhausting, yet I know it is also short lived and how quickly we forget these exhausting times. So, as far as being healthy is concerned Audrey looks great! She's eating well, gaining well and is a healthy little one. The only area of concern is her extension. Which basically means she has a really straight back and she really enjoys her arms just kind of hanging out. The reason for this is that she wasn't in the womb long enough to be in the fetal position. Therefore, she never had to be curled up with her arms and legs in tight. This is the exact reason for the extension, she likes to sit straight up. I guess a plus would be that she has great posture. The neonatalogist has referred Audrey to a Physical Therapist for therapy once a week. Audrey will return to the follow-up clinic shortly after her first birthday. Amazing how time flies, her first birthday will be here before we know it! Did I mention....Audrey rolled over on January 20! It may have been a fluke, because it hasn't happened since. I have plenty of footage after her first roll, she tried really hard but couldn't quite stick it again. This is one of those times I wish God would tap me on the shoulder..."Kodak moment about to happen" How I'd love to have all those little firsts on film.
Exhibit A-in the photo
Exhibit B-Exiting the photo
Love Struck Dawson and Stephanie
I think that sums up all you've missed in a nutshell. It's now 5:45 am on Friday morning and my baby girl has graced me with her presence since 5:15. She must have known how much I've been wanting to update our blog, huh. It's now time to get ready for work! Many hugs to each of you. I hope you all had a very Merry Christmas and that your New Year has started off well! My goal is to post on Thursdays, so feel free to check back! I'm sure we'll have many tales to share.
Monday, December 22, 2008
One Packed-Full Post!
- When I am confused, He offers his plan. Jesus is our "Wonderful Counselor" and He makes the plans. "Many are the plans in a man's heart, but it is the Lord's purpose that prevails." Proverbs 19:21
- When I am weak, He offers his power. Jesus is our "Mighty God" and He makes the plans work.
- When I am alone, He offers His presence. Jesus is our "Everlasting Father" forever.
- When I am disturbed, He offers His peace. Jesus is the "Prince of Peace." "I have told you these things, so that in Me you may have peace. In this world you will have trouble. But take Heart! I have overcome the world." John 16:33
Mommy, Dawson & Nina ready for The Nutcracker
Dawson enjoying his gift from Nina, how fitting!
Ok, so it's really late and I gotta catch some zzzz's before Audrey wakes up for her first late night, early morning feeding! More to come...
Merry Christmas!
Love,
Jenn
Monday, December 15, 2008
A Visitor in the Troyer Home
Tuesday, December 9, 2008
For Audrey and Olivia
Just some photos to share from December 7, TTTS Awareness Day. We lit candles for Audrey at 5:10 and Olivia at 5:15. These candles are not just for my girls. They are for each set of twins that has to go through the trials of TTTS and for the mother that carries them. They are for the sisters and brothers that are often left in the care of others while their Mommy and Daddy are doing whats best for their twins. They are for every lady that I have meant through the TTTS website, you each have a special place in my heart. 


Audrey-my amazing, wonderful miracle from God.
Olivia-my daughter that I will always miss and wonder what life would've been like with you here. I know you are safe in His hands and one day I will hold you in mine.
Thursday, December 4, 2008
Canon Rebel Raffle - "Rebel For A Cause"
So, you gotta check this out! What a raffle...I'm talkin' huge, gotta give it a shot raffle! For all of you photography fans that love to catch your family in pictures...this ones for you! MckMama, mother of 4 little ones, started this raffle to raise money for 3 different charities: String of Pearls, No Hands but Ours, and the Elison Project. You can learn all about these organization through MckMama's Blog, My Charming Kids. All you have to do is buy a raffle ticket for $10 a piece, the more you buy, the more chances you have to win! Each one you purchase will enter you in the Rebel For a Cause Raffle to win a 12.2 megapixel Canon Rebel XSi with 2 lenses, a high speed memory card, camera carrying case, custom made camera strap, 16x20 canvas print of a photo of yours, AND a blog makeover (if you have one of course). Don't miss out on this great opportunity to win great prizes and even more importantly the opportunity to benefit 3 great organizations! Good Luck!
Wednesday, December 3, 2008
Close to my heart...
The day we walked into CFCC was one of the most difficult days in my life. A day that I was full of hope, but honestly scared to death. It was the beginning of an extremely painful and heartbreaking journey. I look at Audrey laying on the floor beside me and my heart breaks. It breaks because I love her so much and it breaks because I wish so bad that we would've been one of the families that got to bring home two healthy babies...Audrey and Olivia.
If you're reading my blog you probably know the story of Audrey and Olivia . This Sunday, December 7, is World TTTS Awareness Day and December is International TTTS awareness month. I will be donating to the TTTS Foundation every year on dates that will always be close to my heart. Please, if you are considering making a donation this time of year think about donating to the TTTS Foundation. Your generosity will enable this organization to continue their mission to help families try to save their babies and bring comfort to those experiencing devastating losses, special needs, and NICU struggles. All babies deserve a chance.
I feel very fortunate to have received the care that I did, my doctors who new they couldn't help me sent me to someone they thought could. Not all medical professionals do this. The TTTS foundation is an organization that is making a difference in the medical profession. They are getting crucial information regarding TTTS to medical professionals all over the world.
The TTTS Foundation website has a message board that has been a blessing to me throughout our journey. I had the support of other mothers who had been there and who were in the same position as me when my girls were diagnosed with TTTS. The ladies I have met on this board are still a part of my life. I receive so much support on the Bereavement-Loss of Your Twin Message Board. It is specifically for parents who have experienced twin to twin transfusion syndrome resulting in the loss of one of their twins or triplets. This board was created to comfort and help parents who know the pulling and tugging of your sorrow and joy. It is hard to explain the feelings associated with this disease. Truly only those who have been through it and have had the same outcome can understand the pain and joy that comes with it.
I am so thankful for this organization and for Mary Slaman-Forsythe the Founder and President. Please take the time to click on the link at the top of my site and check out what this organization is doing to save babies and the dreams of their mothers.
Love,
Jenn

