Today, I took Abi to get her ears pierced. Michelle & Hadley came along, & Chelle got Hadley's ear's pierced too! I had to help hold Abi down. She hated me touching her head. She screamed & cried. I was a sweaty mess afterward. The lady that pierced her ears gave her a sucker and instead of Abi sucking on it, she bit it & ate it fast. She ended up getting 2 more suckers to keep her occupied. So far, she hasn't bothered them. She looks darling!
Friday, March 12, 2010
Earrings!
Today, I took Abi to get her ears pierced. Michelle & Hadley came along, & Chelle got Hadley's ear's pierced too! I had to help hold Abi down. She hated me touching her head. She screamed & cried. I was a sweaty mess afterward. The lady that pierced her ears gave her a sucker and instead of Abi sucking on it, she bit it & ate it fast. She ended up getting 2 more suckers to keep her occupied. So far, she hasn't bothered them. She looks darling!
Monday, February 22, 2010
:Walking:
Photo and video editing at www.OneTrueMedia.com
This is one of my proudest moments of being a Mom! We've been working with Abi to walk for awhile now, but tonight, she was ready to show me what she has been hiding.
Right before I took this video (along with 8 other videos) of her walking, I looked over at the couch, and Abi had let go & had done a total 360 turn around without any help or support. So, that led me to see what she could do walking wise. She definitely has proven herself that she can do things that we were told that she may never do.
I definitely cried tears of joy tonight & Lyvie screamed lots of "Yay Abi!" I couldn't have captured these moments without the help of Lyvie.
Right before I took this video (along with 8 other videos) of her walking, I looked over at the couch, and Abi had let go & had done a total 360 turn around without any help or support. So, that led me to see what she could do walking wise. She definitely has proven herself that she can do things that we were told that she may never do.
I definitely cried tears of joy tonight & Lyvie screamed lots of "Yay Abi!" I couldn't have captured these moments without the help of Lyvie.
I am one happy mommy!
I love my girls!
P.S. Sorry for a naked little girl, we were just getting ready to have a bath.
Monday, August 31, 2009
What a way to end the month!
She has taken off these last couple of months. The milestones she accomplishes, whether they are BIG or SMALL, are HUGE to us! We are amazed at everything she is doing. Every week she is doing something new.
Thursday, August 13, 2009
Happy 2nd Birthday!!!
August 12 (Abi's birthday party) & 13 (Abi's birthday)
Abi, we have loved having you as a part of our family! You never cease to amaze us. We are excited to see what you will be doing now that you are 2!
We Love You FOREVER!!!
Sunday, July 19, 2009
Monday, June 22, 2009
Sunday, May 31, 2009
May Update:
P.S. We took her binky away. =)
Friday, April 3, 2009
ABIGAYLE
Anyway, it's been 2 weeks since Abi has been off of the ACTH. What a change we have seen in her. We literally have a brand new girl. A girl we've never seen before. She is doing so much more than she ever was before she was on the ACTH. She regressed while on it, but most everything & MORE came back as soon as she was finished with the treatments. She is rolling, starting to clap (only on her time), waves "Bye-Bye" & "Hi". She's grabbing for things, using BOTH hands, hitting toys together, studying things... such as our faces, designs, pictures, things she never noticed before. She also bounces to music, almost can pull herself up from a laying position to a sitting position, & grab & hold onto finger foods. The biggest accomplishment we have seen in Abi, is she laughs. She didn't laugh much before, & never laughed while on the ACTH. To see a new light in her eyes & to finally hear a real laugh come out of her is amazing!!! Her weight is slowly decreasing. But we have gotten used to her chubby self. She has been wearing size 3T tops. So, pretty much sharing shirts with Lyvie. Lyvie thinks it's pretty cool, so I can't complain. She is still pretty hairy, but we've have been told by many & also Dr. L that the hair will fall out. I don't mind how thick the hair on her head has gotten or even how long her eyelashes are. But her brows need a definite waxing!!! She is still cute though. Nurse Julie came by yesterday to take one last look at Abi & checked her vitals. I am happy to say everything is normal. What a relief!!! As for her spasms...they are back. She is having one or two daily. BUT they are only when she is woken up from sleeping, or startled while sleeping. They still look like the Infantile Spasms, but we are still hoping that they'll go away. Dr. L informed me that it may take up to 6 weeks until we see a change with the spasms. He said the ACTH is just waiting it's turn. As for groups. She can go out in public in about 2 more weeks. I have to admit, we have taken her out a few times. She cannot be immunized for another 3 months & cannot be around anyone who has been recently vaccinated with LIVE vaccines... such as Chicken Pox, MMR, or Oral Polio vaccinations.
We are so happy to have our "OLD" Abi back, & also the "NEW" Abi. She is so fun! And it is fun to watch her & Lyvie or any kid interact. She's a very happy girl. Sleeps great! And is learning new things everyday!!!
Here is a video I took of Abi laughing last night. I have never seen her laugh this much in her whole life. So it's way fun to watch!
Monday, March 23, 2009
Last few weeks on ACTH:
I cannot tell you how happy we are to be finished with the treatments. This was such a big decision that we had to make for Abi. I've had many people ask me if we would ever do another round of the ACTH for Abi, and my answer is NO!!! Yes, we've received positive feed from it. We've seen her spasms go from 3 or 4 a day, to roughly 1, maybe 2, a week. But in the long run... so not worth the stress on her. She regressed in everything that she had learned, but she also started to do things that we weren't expecting her to do so quick. To see the stress it put on her body, was heartbreaking. Worrying if she was going make it through one more day, was exhausting in every way you can imagine. It was a very risky treatment, & we feel like if we cannot completely get rid of her Infantile Spasms, then that is who she is! Abi, may always be our Abi who has seizures. But that's okay. We have come to accept that. I have grown so much closer to my parents & siblings, & to Dave's parents & siblings. Not only have I grown closer to them, but I have grown closer to our Heavenly Father. I had to put my complete trust & faith in him. ( I still do!) I have learned so much more about myself & about what I CAN handle. People have said, "I don't know how you do it. I don't think I could do it." We did this for Abi. We made it a routine & was able to get through it. When its your child or someone you love, you would be surprised what you CAN do. We are not out of the woods yet. Now it's just a waiting game. The spasms can come back, but hopefully they won't. It's all up to the Lord.
I want Abi to know how truly amazing I think she is. She is my hero! To agree to such a challenge while in heaven, makes me admire her more than words can say. She is very loving, unselfish, happy, STRONG, contagious, determined, lovable, beautiful, sweet, easy going (when not on ACTH), & the list could go on & on. I love her with all my heart & soul. My girls are my world!!! I am proud to say I am their mom! I am proud of Abi, & the example she is in our home. She is a very special girl! She has a spirit about her that I cannot describe. You have to be around her to know. I am thankful for the Lord & for him giving Dave & I the opportunity to raise such a choice spirit. I love you forever, Abi!
Sunday, February 22, 2009
Water Retention
This is a picture of Abi, a week before starting her on the ACTH
AND
This is Abi at the beginning of Week 6 on the ACTH
One of the side effects of the ACTH steroid is, water retention. This is by far the most swollen we have seen Abi. You can see how swollen she is throughout her body, but her face is the most noticeable.AND
This is Abi at the beginning of Week 6 on the ACTH
Carol, one of her weekend nurses came on Saturday & couldn't believe the change in her. It is definitely sad to see her go through all of this. She isn't moving around as much as she used to. But the Dr. said once she's completely off the treatment, our precious Abi should return back to herself. I'm excited for that day.
As for the RSV, I think we're almost out of the woods. She's doing much better, & just has the lingering cough. She is still pretty irritable & doesn't like Mom so much. The nurses & I have come to the conclusion of why she isn't too fond of me right now; It's because I am helping hold her still while she gets her shot & checked daily. Daddy is her rescuer & that is why she wants him constantly. Sad, but TRUE! Also, she's a big fan of Grandma Jaques too!
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