Tuesday, July 6, 2010
Summertime...
Posted by 4Sydney at 9:03 PM 0 comments
Sunday, June 13, 2010
Lost & Found...
Posted by 4Sydney at 9:16 PM 0 comments
Wednesday, May 12, 2010
Sydneyrella turns 1!!!
Posted by 4Sydney at 8:01 PM 0 comments
Thursday, April 15, 2010
Sydney the Signer
Here is a picture of Sydney after dyeing Easter eggs with her cousins. I think she splashed more dye on herself than on the egg, then she cracked them...oh well. She had fun hunting for eggs at Grandpa and Grandma's house. She didn't know what to think of the Easter bunny. She didn't cry, she just looked at him wide-eyed trying to figure him out. She also enjoyed her feast at her other Grandma's house, spending time with the family and playing with her cousins.
It's really exciting now that Sydney is starting to sign. My biggest fear after finding out she had a hearing loss was that I wouldn't be able to communicate with her. I sign and talk to her constantly and some days I wondered if she was understanding any of this. It is a wonderful feeling now that she is signing back and babbling so much.
Today I took her to the library to hear a story being read. Then we sang Twinkle Twinkle (one of her favs). After the song was over she signed "again". It was too cute. I felt bad that we couldn't oblige. It was getting close to lunch time and I was worried about how much longer she was going to last before she started getting fussy. She let me know by signing "food". I rushed out of their quickly and got her a cracker before the melt down began. It great to be able to communicate with her at such a young age. It just shows that baby's are smart thinking individuals and if you give them the tools to communicate they can express themselves.
Posted by 4Sydney at 2:47 PM 0 comments
Thursday, March 18, 2010
Doctors, babbles and bubbles....
It's been a while since I've posted last. I guess I got caught up in the craziness of daily life. I did't know a 10 month old could command so much attention. Sydney has been a busy girl between school, doctor's appointments and playing at the park.
We finally got her test results from the Usher Syndrome after an axious month of waiting. The test came up negative for the 4 of the 6 known types of Ushers they are able to test for. I was able to exhale just a little.
Syd had a couple of colds over the holidays that left her with fluid in her ears. I noticed that she seemed a little less responsive. We went to see her audi and sure enough her typanogram was flat indicating that she has flud in both ears. It took a good three months for it to clear up. After many booth tests and ENT appointments we finally got the good news that the fluid has drained (yeah!). The booth tests actually showed better responses in her right ear than her original ABR which was a little good news. I am glad we didn't have to get tubes, hopefully this won't be a reoccurring problem.
She also had an "in the ear" measure of her hearing aids which I read in a hearing loss magazine should always be done. It was quite the process and her poor 36 week pregnant audi in a 85 degree office was so patient with her. Syd has always been very good about allowing the audi to mess with her ears. It was a big feat trying to get this needle thin rubber tube in her ear with the hearing aid without it falling out. We got it done and she made some adjustments to her aids as a result.
Syd had this puzzling head tilt for the first 7-8 months of her life. It would last for months at a time and would switch from left to right. The PT ruled out torticollis. It seems to have gone away for the most part. But every now and then she will wake up with a head tilt. She will be lethargic and pale, and then vommit. It wasn't until this time around that it is not a stomach virus. This is the second or third time it has occured and seems to happen about once a month. What really concerned me this time was her eyes were jutting back and forth like she was watching the room spin. I thought maybe she was experiencing vertigo. So I looked up the symptoms on the internet and I came across a condtioncalled paroxysmal torrticollis which describes her symptoms exactly. Many times it is a benign condition that can eventually lead to vertigo and migraines later in life (if you want to call that benign...) and sometimes it can be a symptom of a larger condition. So now I am on a mission to find out what is going on. Her MRI came up clear which is a huge relief. We are meeting with an ENT next week so hopefully he can give us some more insight.
On a brighter note. Sydney started babbling about a 6 weeks ago and hasn't been quiet since. She says "baba" "dada", and seems to enjoy babbling at all waking hours which for her starts at 0530 (ughh). It's so great and cute and just love hearing her little voice. The beast is when she gets excited, like when I took her to see the fish at the pet store today. She can't contain herself and screams an ear piercing scream at the top of her lungs. I am surprised the fish were able to take it. People were starting to give me dirty looks, I was torn whether to muffle her a little because I was just happy she was so vocal about it.
Syd has made huge progress in the last couple of months. I do sign with her throughout the day as well as work with her on her speech. It is amazing how much she comprehends. I will verbally ask her to get some books to read, and she will crawl over to her books and pull them off the shelf. This morning I asked her where her foot was, and she grabbed onto it. And this eveing she she did the same for my nose and eyes. I am so happy I have this opportunity to spend with Sydney. Nothing is more rewarding and fulfilling than spending the day blowing bubbles and babbling with Syd.
Posted by 4Sydney at 9:55 PM 0 comments
Wednesday, December 23, 2009
Baby no more...
It is amazing how quickly Sydney has grown. Gone is her little infant face and her imobile self. She has taken on the toddler characteristics and is scooting around, but not quite crawling. She is very responsive and social one, always trying to strike up a conversation with a stranger. Her usual babbles consist of "aaaaah" or an earsplitting squeal.
We were thrilled to see her first sign "more". I don't think she knows how to use it in context, but if you say the word "more" she will put her hands together and then look at you patiently waiting.
She visited Santa with her cousins and was happy as could be pulling on his beard (she was making sure he was the real thing). She also really enjoyed Christmas in the Park in San Jose. She loved all the lights and the animated scenes. She bent over backwards to see the snow bubbles falling from the sky. We are very excited to have our first Christmas with her.
Posted by 4Sydney at 11:25 PM 0 comments
Sunday, November 22, 2009
Picnic of Hope...
Sydney's teachers are so wonderful in her early intervention program. They are all so compassionate and passionate about helping deaf and hoh children. One of her teacher's comes to my families house once a month and teaches us sign language and is so patient with our families sarcastic antics.
Another of her teachers just started a meet-up group for all of the local counties deaf and hoh kids. This really means a lot for our family, and others out there that can assimilate with us. We had our first potluck picnic at the park across the street from our house on Saturday. It was rather chilly but when the sun peaked through the clouds it briefly warmed us up. There were about five families that showed up. Everyone was so nice and I was so thrilled to see all the cute kids with their hearing aids and cochlear implants.
Ever since Sydney was diagnosed with a hearing loss I had been in search of people I could relate to that were experiencing the same journey that we are. I managed to find some on-line in forums like Help Kids Hear that made me feel not so alone. Nothing could match actually seeing people face to face and seeing how well their kids are thriving. Hearing all of their experiences gave me the hope that I needed to know that Sydney will be just fine. You would be as amazed as I was to see how cute and wonderful these kids were. They were all so well spoken, I would've never known they were hoh or deaf. I could see some of them signing to their parents from across the park. These parents once were where I am now, and to get the reassurance and see the proof that everything will be OK is all I need for now.
On a different note, please keep Sydney in your thought and prayers that her test for Usher Syndrome comes back negative. We will have to wait a long dreadful two months for the test results. The geneticist was pretty hopeful that this isn't the case, but nonetheless all of these tests are scary until they pass.
Posted by 4Sydney at 10:54 PM 0 comments
