The last few months have flown by for us! Many "Lily anniversaries" have come and gone since the last time we posted. The anniversary of our 1st hospital stay came on Valentine's Day. The anniversary of our 2nd hospital stay and her g-tube procedure came in March. Lastly, the anniversary of Lily's diagnosis came on April 7. It is hard to believe it has been a entire year since we found out that Lily had 1p36. It has been a very fast and event filled year.
In the year since Lily's diagnosis we have seen amazing progress in Lily's abilities. Lily's most recent accomplishment is her vision. In December 2007 Lily stopped looking at us. She had trouble focusing on things other than flashing light toys. It was devastating to us as parents. We wanted our baby girl to see us, smile at us, respond to us. In February of this year we were blessed with an amazing therapist who specializes in Vision Therapy. This therapy has changed our little girl. She is now looking at her brother and sisters. She smiles at us often. She follows toys more readily. She is focusing on the sign language we are trying to teach her so that we can communicate. She still has a long way to go as these moments of vision are brief...but they are there and we are thrilled!
Lily's gross motor skills have definitely taken a backseat to all of her eating, speech and vision accomplishments. In March/April Lily decided that she no longer wanted to stand. She no longer was interested in climbing up the step from the family room to the kitchen. She started throwing her head back violently each time we would put her in a position she did not like. She threw a HUGE temper tantrum at the place that fitted her for a gait trainer. (a special durable walker).
It only took me a month to figure out the problem...Lily's shoes were too small. Yes- it seems like a simple solution - but Lily's feet are really little. She had been wearing a size 4. When you press down on the shoe it seemed like they still fit. But with her orthodics...it must have been too tight. We got some new shoes a couple of weeks ago. She only increased to 4 1/2...but that was enough! She is much happier and our PT is relieved! We hope to have Lily using her gait trainer by this summer!
We are back to teething again - 2 year molars. These teeth seem to grow in the middle of the night...like 4am. Tylenol is once again our close friend. I make sure to give Lily her favorite blanket as often as possible - so that she can chew on it instead of her hands.
Also- this spring Lily went on several new adventures. I have been keeping her close to home this winter trying to avoid the nasty germs. But on Spring Break I took a leap of faith and took her out! We experienced all sorts of new things. We took Lily and her siblings to the Indianapolis Children's Museum, Monkey Joes (bounce house place) and Great Wolf Lodge in Ohio. Lily had a blast and handled all of the noise and over-stimulation very well.
Next Thursday our baby Lily turns TWO! What a wild ride these last two years have been! God has taken care of us thus far...so we are going to continue to put our faith in HIM and see what the next adventure will be!
***Jason and I continue to work on this year's 1p36 Deletion Conference. We are currently raising as many funds as possible for the conference. For more information about the conference or to register please visit http://1p36conference.blogspot.com.
***Lastly, I would like to ask for prayers for all those 1p36 families who have lost their children this past year. These are amazing families dealing with great pain and sadness.
Pumpkin Time Already!
5 years ago
6 comments:
Hi Julie and Jason,
My name is Kim and my daughter Sophie is 7 and newly diagnosed with 1p36. She had the genetic testing done when she was 6 months, but it showed up "normal." I am very excited about the conference and hope to meet a lot of people there. I hope that the experiences that we have gone through also we will be able to give some thoughts as well as receive them. are you from indiana? we live in tipton which is about 25 miles straight north of indy on 31. Your daughter caught my attention because she looks SOOOOO much like Sophie did at that age. Sophie also has a gtube. since she loves water we call her our water baby. besides...when other t.d. kids are questioning the tube, I use that little water baby as an example. Works for them. I hope to hear from you and I enjoy reading your blog. ours is sophieajourneyinprogress.blogspot.com. I am still awaiting approval on the yahoo 1p36 group. Not enough is out there on the we to quench my thirst for knowledge. Drs and genetic research is great, but nothing compares to other parents. thanks for posting. respectfully, kim and sophie
i was typing so fast that i made a few grammatical errors. please just try to get the jest of it. my brain has been on overtime the past week. lol. thanks again for all the information that you put on your blog. much appreciation from me and i imagine others new to 1p36
Happy 2nd Birthday Lily! I'm glad to hear about all of her accomplishments. We are all very excited about the conference! I can't believe how long Lily's hair is and how big she looks. The picture of her sitting in the water is adorable. I can't wait for Alayna to do that someday.
Happy Birthday Lily!!!!! Wow, two years old already! I look forward to seeing you guys again this year at conference.
Happy 2nd Birthday Lily! I am so happy you are doing so well. Keep it up!
hi Julie, you will have to check out our post. i put 2 photos of the girls on there. they are so cute. thanks once more for the invitation to come over. i will try to drop off those tubes to you on saturday. glad that i can give you something that will be of use. and youre welcome for her present. cant come empty handed to a sweet little girls birthday day without bearing gifts. kim
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