0 comments Saturday, April 19, 2008

 


 

We are now offering bracelets as a part of our fundraiser to help pay for the numerous adaptive equipment and therapies Gracie needs that insurance does not cover. The bracelets are purple and say "gracie's friends". They are available for $5.00 plus $1.00 shipping. If you would like to support Gracie and purchase a bracelet(s) please click on the PayPal button to the right of this post to place your order and we will mail it to you ASAP! Please pass this on to anyone who may be interested in a bracelet. Thank you to everyone for your support…Gracie sends hugs! J

Thank you to Grandma Jackson who had these bracelets made for us…we love you! J

0 comments

The Beautiful…



 

The Good…

Well, we had great news Wednesday when Gracie's teacher stopped us when we were dropping her off at school. He said they have been discussing with the other teachers and therapists to move her up next year into a more advanced class! They said she continues to amaze them everyday with how quickly she learns and how smart she is. They already moved her into a more advanced class at the beginning of this year and she is ready to move up again. This will still be a special needs class although most of the kids are able to walk but some of them cannot talk as well and have developmental disabilities. Her teacher (Mr. Mike) says that she is well on her way to learning to read with how quickly she recognizes words! When we get her "talking tool device" we will be able to understand even more of what she understands! We are so excited for her and so proud! She also took 2 steps without holding on to anything a couple of days ago…but they were very small and unbalanced and she fell. Don't get too excited though because she is a long way from walking and we are still not sure she will ever walk without some sort of walker assistance but this was so cool to watch and she was so excited and laughing so hard she couldn't keep her balance. Her torso is so weak and her balance is so bad it makes it so hard for her. We are hoping to get her into hippotherapy (horse riding therapy)…this is supposed to really help to strengthen her torso. Unfortunately, there is a 2 year waiting list as there are not many horse therapy places around, so we just hope they have some cancellations and it won't take 2 yrs. Her PT also got her to walk about 10 steps in her walker with only the sling seat in it and no other constraints! Also, Gracie has never said a single word…she only makes sounds like an infant would goo-goo, gah-gah, etc. Last night Jerry was asking her if she wanted to go nite-nite and she shook her head no and said no!!!! It wasn't a clear no, but it was more like na…but it was a definite no for her along with the head nod no! We were so excited we kept asking her questions we knew she would say no to and she continued to say it again a few times more and then got bored of it…we wanted to hear it all night! How many parents want their kids to tell them no? Not many but she can tell us no all she wants! J

 

The Bad…

Gracie had a major seizure Friday morning. She woke up around 1:30am ready to go for the day (of course she was the only one ready to wake up)! She ate and watched cartoons and then was ready to go back to sleep around 5:30am. She was asleep for about 3 minutes and started seizing. It was a big one like she used to have before she started on the Keppra medicine. Her entire left side was tight and jerking so hard...it was so heart breaking . L We had to give her the Diastat medicine to stop it, which we haven't had to do for 3 years. Gracie didn't even start having seizures until she was 2yrs old and they then put her on Keppra and it kept her seizure free again for 2 ½ yrs and when she started having them again they were very small and stopped on their own after just a couple of minutes. Unfortunately, this time was different so now her neurologist wants to check her Keppra level to see if it's at the level it should be to "work". They will just have to draw her blood to check it so not too invasive. The strange thing about her seizures is that we have noticed a pattern that every time she has one she starts doing something new. Almost without fail, when she starts doing something new, shortly after she will have a seizure. Days before this seizure she started really trying to walk (like I mentioned above in the good) and then a day after the seizure she became much more vocal and started saying no! I know seizures are not good and we absolutely hate it when she has them but it always seems like something good happens around the time she has them…really weird!

D

0 comments Tuesday, April 8, 2008

Well, this morning Gracie woke up with a little rash on her nose, it was such a small area and only on her nose (at the time) that we didn't think much of it.  We went through our normal weekday morning getting ready for school routine and she seemed fine, laughing at Ari and Logan and watching cartoons.  When we got to school I noticed her cheeks looked a little red/rashy too so I had the nurse take a look at her and she wasn't sure either and just thought maybe it was something that she was allergic to that touched her face or something because she had no fever and was acting fine.  I told them to call me if it got worse or if she had a fever, etc.  Well, she made it through the day and when I went to pick her up I noticed her face was still rashy (it seemed worse than earlier that morning).  She did seem okay still and was happy and smiling when she saw me and Logan...though she seemed a little "slow" in responding to me…kind of delayed responses.  By the time we got home and I brought her in the house it had spread to her neck and behind her ears and it had heat when you touched it.  I called for Jerry to come up from the office and he noticed too that it had gotten worse so we checked her temp and she had 100.7.   Of course her regular doc office was closed by then so we took her to urgent care.  They tested her for strep and that was negative.  But the xrays showed she has double "walking" pneumonia. Walking they call it because she really didn't have any typical signs of pneumonia, no congestion or high fever, lethargy, etc. Like she was walking (don't I wish walking) around with it but not really sick…if that makes sense! He put her on amoxicillin because it's been less than 30 days since she was on azithromycin for her bronchitis and sinus infection. Poor Gracie L She is such a trooper…she still seems fine though, nothing like the pneumonia she's had in the past. I am hoping that's because maybe we caught this one early!

0 comments Friday, April 4, 2008

I just have to share this story on Yahoo I came across of this amazing 10yr old girl Jemma with cerebral palsy.  She is non-verbal but "speaks" more than any of us ever will!  It's what we say about Gracie all the time…there is so much inside that precious head but she just can't say it. L We are in the process of working with her speech therapists to find her the right talking tool similar to the one the girl has in the story. Gracie does pretty well with her sign but as she is getting bigger and smarter J so she has more to say than her fine motor skills will allow her to sign. They have been doing some testing with Gracie at school and she is able to recognize 8 out of 10 sight words. Also, yesterday they showed her the names of the kids in her class and asked her "which name is Sarah, Devin, etc." and she got them all right! This is a big sign that she will probably be able to read someday! How awesome for her to be able to enjoy a great book! J


Check out the story…here's the link…and a correction for the news guy telling the story, cerebral palsy is not a disease, it's a condition resulting from an injury to the brain....just had to say that!


Watch Jemma's Story