Monday, December 22, 2008

Lily's Busy Fall


Hi Everyone! Merry Christmas! I cannot believe we have not posted since September. We are so sorry. There is not enough time in the day to do all that needs to be done...so the blog has suffered. Many wonderful things have happened in the last 3 months - we have lots to tell about our Miss Lily!

Crawling!- October
Our biggest news is that Lily is now crawling! It is amazing how her motor-planning works. We show her the same positions over and over and over. Then all of a sudden something clicks. Once she figures something out - there is no stopping her! Jason caught her one day secretly moving in her crib - getting on her hands and knees and trying to go forward. But on Monday, October 13 - she moved on her floor in her bedroom - 3 crawls forward. I was there with the girls and we were all jumping up down screaming "She's doing it...she's doing it! ". Within two weeks she had put it all together and she was all over the floor discovering toys, cabinets, magazines, etc. She moves from room to room getting into all sorts of mischielf! I love it!!!!


Tall Kneeling - November/December
Lily is now tall kneeling (on her knees) all on her own. She started in her bed - reaching for the buttons on her mobile. Now she will get as tall as she can to get what she wants. It is awesome!. With her orthodics on her feet she can stand against a bench/table for a long period of time. A few weeks ago we took our PT down to our "scary" basement full of the older kids toys. The PT loves the train table for Lily. It is the perfect height for working on cruising. She puts a toy at one end and then moves Lily's feet for her to show her how to cruise.

We are also working on getting Lily to go up steps. She is having trouble getting from the kneeling position to standing and then putting her knees up. We just have to keep showing her over and over. She has the strength...just not the motor planning.


The Motherload of Teeth - October/November
Lily is getting 8 teeth all at once...yes...8. 4 molars and all 4 incisers! Needless to say it has been a very sleepless month. She has been sleeping a lot in our bed at night. We don't care where she sleeps as long as she sleeps. One week we were up 2-3 hours a night in the middle of the night. Lily never really cries unless there is something very wrong. She must be in a ton of pain. There are huge tears often.

Eating! - September/October/November/December
We started a new speech therapist at the end of September. She is awesome! She is so good with Lily. She is very focused on the eating portion of speech therapy. In the last 2.5 months she has gotten Lily from eating 1/2 jar of #1 baby food to eating small pieces of Cheerios, bananas, oatmeal, avocado and shredded cheese! Over the years our therapist has gotten 21 kids off g-tubes. I am confident that with time she will be able to do the same with Lily. We just were approved at our last big First Steps meeting to get an additional speech a week. So now we can focus one session on eating and one on speech! Lily is signing a few signs inconsistently - "more", "bye, bye", clapping. But she is doing a lot of mimicking- sounds we make with our mouths. She will say"ma" when repeating me and will make the same inflections as we do when we say "byiiiii". We also got a different high chair and it has made a HUGE difference in the way Lily eats. The chair fits her much better. A big thanks goes to Nana Cherryl for shipping the chair from Florida to Indiana.

Ear Infection - December
We are back to having crazy ear infections. The same ear that bothered her this summer is at it again. Lily has tubes. This kind of stuff should not be happening. There is no drainage from the tubes. She is currently on Omnicef. She is taking this one pretty hard and is in our bed now almost every night at some point. I am starting to think she really just wants to be close to me - which I cannot complain about. All last year she didn't even act like she knew me...so I really do like it. She goes to bed well for babysitters and my sister. But when it is my turn...nothing will do but me holding her! The doctor thinks maybe the tube is not in the right place. Once the infection goes away we are going to go get it checked again.

G-tube - September/October
When we were at the conference I mentioned to everyone that we were thinking about having a procedure done for Lily's g-tube granulation. After talking to several people at the conference including a developmental geneticist - we decided against the procedure. Instead someone from the Yahoo user group pointed me towards a newsletter than highlights articles about special needs kids. One of the articles discussed this compound of Chloestramyne (sp?) and Aquaphor mixed together. I called my GI doc about it and showed them the web site. They called it in to a special compounding pharmacy. This compound is amazing!! You should see her tube now. There is virtually no granulation at all. Goodbye horrid silver nitrate sticks!
First Haircut - November
Before Thanksgiving Lily got her first haircut. She was awesome! My hairstylist Lisa - who has a child with Down Syndrome came to our house to give Lily her first cut. Lisa was so patient and gave Lily a great cut! All of Lily's curls are coming out now...so cute!

Overall we are doing really well right now. This has been a really fun time for us with Lily. She is interacting with Nathan, Ella and Ava. They love to play with her all of the time. Ella thinks she is a little Mommy and would carry Lily all around the house if we would let her! Keeping Lily well has been our biggest challenge. She seems to pick up bugs so easily. We have her on Probiotics all of the time. We do not take her to any kind of daycares (gym/church). We have to be very careful where we do take her. Washing hands has become a full time job around here! We are keeping the soap companies in business!

We want to thank all of our family and friends for all of the amazing love and support you have given us this year. You all have carried us through this difficult and confusing year. Your prayers have enabled us to get through even the hardest of days. We love you and thank God for you every day.

We are looking forward to 2009 and the many surprises that await us. We feel that it will be a great year for our Lily.

Take care and God Bless! Merry Christmas!!



5 comments:

Kimberly Whitaker said...

I am so glad to see an update. I know you guys have been busy as we have too. It sounds like things are really moving forward with Lily. I can not belive how old she looks from Sept. Keep working on that feeding. I know the tube will be removed and I will be pray for this to be a fast moving thing!!!!!

Angie said...

Oh my goodness she is doing absolutely awesome! I can't believe how well she crawls and especially on a slick floor with PJ's on! It is amazing to see how strong she is. Alayna really lacks that strength. I can't even get her to get on all fours with her arms straight. It is frustrating, but I must be patient. Her facial expressions in the video while she is eating shows how much she is comprehending and understanding what you are saying. You are doing a wonderful job with her and it looks like you have great therapy. I'll be that feeding tube is out very soon because it looks like she is doing very well eating. Keep up the good work and we will definitely be meeting you all in person in July!

Anonymous said...

Hi Julie!

Lily looks great! I can't believe all that she, you, Jason and your family have been through this year. Lily is so lucky to have you and Jason as parents. God knows these things. You all are in my prayers.

I hope you had a great Birthday! I think of you often, I'm sorry time gets away from me. I'm sure you have your hands full too! Hang in there!

Kris Moore

Genevieve Ross said...

Wow, I can't believe how much Lily has changed since September! You guys are doing such a wonderful job at pushing her. Keep up the eating- she will get it she is a smart little girl. Thanks for the update, I am glad that things are going so well for you all.

Karen said...

WOW..Lilly is doing so well. I loved watching the video of her eating and the smile she would give to you. That just made my heart melt. I love it when Kylee smiles at me. Sounds like you have a great speech therapist. If she had any great tips you should post them on the forum. I would love to hear some of them. Kylee is a half of jar eater but we are working hard to increase it so we can get rid of the tube.
Keep up the great work!!!!
Karen M