We are trying to decide what color to paint the kitchen to lighten it up :) |
The color on the left of the door is popcorn and the color on the right is cracked wheat |
It finally stopped raining so the kids could play outside. This is how they came in :) :) |
I bought some washable paint and they were so happy to paint!! |
Their finished masterpieces! |
So happy to paint the table cover! |
I know it is better than snow, but this is FL darn it!
I did forget to mention that while in Shriners they were able to weigh and measure Gerri and she has grown 4 inches since coming home!!! unfortunately she has lost 2 pounds :( but I think it is because she is SO much more active!! Both Gerri and Danny are low on the scale so we are trying to get calories in them.
I told them they could have my fat and they both just laughed at me! How ironic that I have been on diets my whole adult life and 2 out of 3 of my kids have to GAIN weight!!
We have not told Gerri about the surgery in the future, since we don't know when it will be it makes no sense to worry her. She knows she is going back for 3 casts. She is happy that her siblings will alternate going with us.
The phone rang the other night and it was Dr vB's asst!! She is so nice. We talked about the schedule and when she thought we might have surgery and she just doesn't know. There are 50 kids on the surgery list and it totally depends on how long the surgery is. Gerri's surgery will be about 5-6 hours! And she will be in the hospital for 4-5 days :( She will be in full cast from chest to toes for 6 weeks! She may have to be home schooled the whole time too.
The current plan is for ms V and I to go and Dan stay home with Danny so he would not miss school. But the surgery might not be till the end of school. So it may be a family affair.
I have to check to see if they would allow ms v to visit at the hospital with me if it is just us. Does anyone know the rules at shriners?? She is 4.
I have Gerri's IEP meeting next week, this is just the meeting where we meet to approve her being tested by OT and PT, then we have to wait for the evaluations, then meet to write up her IEP. So I figure by the time we actually have this done school will be out!!! It is so frustrating that it takes the school system from August to February to get to this point, and she is still not getting any services!! The school was not going to do anything for her since they said she is not academically delayed (which she is!) but luckily the OT told them FL law has a provision for children with physical disabilities!!
I had Danny's RTI meeting last week. Everyone was in agreement that he has not moved up the learning curve for his class. He has actually been approved to go into ESE services. We are waiting on the school psychologist to write up a report and get it signed off by the asst principal. Then we have to have a meeting to write up his IEP. So it will be quite a while before he gets ESE services. He still gets his 1/2 hour of reading coaching, but he is still not reading. :( It is really harder with a child that has a disability that is not visible. Even with medication he has a very hard time in the morning and last afternoon. His teacher does not notice much difference so we are debating him even taking it. Dan thinks Danny is more emotional now too. The medicine does give him definate highs and lows :( Here is a short video taken before school this past week.
Here is how they ended the night tonight!! Watching Tad :) |
5 comments:
The kids are are all precious. I did want to say that what you describe in Danny sounds a lot like FAS or FAE. The attention, behavior, processing issues, and short term memory are ALL signs of this...
Have you had him evaluated?
Awww this breaks my heart. I really really wish you were in NY so that we could work with him! If he has issues with his short term memory he really needs multisensory curriculum. He shouldn't have to make a herculean effort for reading at this age. There's a quote that my program lives by "If he cannot learn the way we teach then we better teach the way he can learn"
He's so precious and I know you're an awesome advocate for him.
I felt like it was mean to keep pushing him over and over. How could he calm himself down, when for 4+ min. you were nagging at him? I think your older kids are afraid of you. Afraid that whatever response they give you will always be wrong. No wonder Geri doesn't tell you when she is in pain. If she says "yes", then you ask her "why didn't you tell me?". If she says "No, then her pain doesn't get treated.
Unless the rules have changed (which according the website they haven't) Miss V should be able to visit Gerri in the hospital after her surgery (only 1 parent is allowed to stay bedside over night). They may not let her in the PICU or they may ask to be certain she hasn't been ill. When I was inpatient I always had little people in my room and I know siblings have visited other kids in PICU. Kids w/ hip surgeries (and back and fixators ect) are usually take to the PICU for the first 24 hrs then transferred back to the floor. Oh and I LOVE Mimi too!
hi there. i've been teaching ESL in 2nd gr for 7 yrs now. what i can tell you is that all children are different. they learn at diff levels and they learn in diff ways. i didn't see the video(it's not showing for me for some reason), so i can't comment on danny's level. but i have a lot of experience with his age, and a lot of experience in teaching reading. there is a wonderful website called starfall.com i recommend this site for many of my parents. it has all different levels for reading, and it's done in a fun way. who wants to read when it's boring, right? ;)
if danny were my student i would use a lot of TPR (total physical response). he is the kind of learner that needs to feel, see, smell, hear, and even taste in order to hold onto the information he's learning. rather than just showing pictures of things, he may need to actually see/hold something in order to remember facts about it.
there are many other wonderful websites and learning tools available. for example, i just bought my son a toy from leap frog where he can learn how to build three letter words. you can go to leapfrog.com to see all of their learning toys. crayola.com has some really great printable activities (and they're free too, yay!).
sorry to go on and on. but i can see that you're trying so hard and feeling frustrated. we all have our good days and bad days. the important thing is to keep on going and to keep trying. i think it's wonderful that you care so much about your children. you're doing a great job. well done! :)
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