Austin will be starting the 4th grade this year. Typically since he has started school I have made an appt. with the new teacher for the year and talked to them about CF and they were welcome to ask any questions they had for me regarding Austin and CF/
The situation this year is different. He will have a home room teacher and then they will be rotating clasess. He will have 4 different teachers this year. I could meet with his homeroom teacher but will she inform the others or should I just set up a time to meet with all four of them at once.
I also sometimes feel a little awkward talking to some of the teachers. Only because there is another child at the school who also has CF and she is a sophmore this year. Our school is small grades K thru 12. I don't know if her mother tlaks to the teachers or not about her condition. She is more of a keep to yourself type of Mother.
Me on the other hand I wanna make sure my child is being looked after and is taking all precautions.
Austin also has a shunt in his head due to hydrocephalus and Arnold Chirai Malformation.
I have given the previous teachers info about CF and they have placed it into a folder and have passed it down every year so far.
I also tlaked to the NEW principal when i dropped Austin off at summer school and she said in all her years she has not EVER had one child with Cysitc Fibrosis. So I guess it would be time to educate her also.
Any suggestions are welcome!
The situation this year is different. He will have a home room teacher and then they will be rotating clasess. He will have 4 different teachers this year. I could meet with his homeroom teacher but will she inform the others or should I just set up a time to meet with all four of them at once.
I also sometimes feel a little awkward talking to some of the teachers. Only because there is another child at the school who also has CF and she is a sophmore this year. Our school is small grades K thru 12. I don't know if her mother tlaks to the teachers or not about her condition. She is more of a keep to yourself type of Mother.
Me on the other hand I wanna make sure my child is being looked after and is taking all precautions.
Austin also has a shunt in his head due to hydrocephalus and Arnold Chirai Malformation.
I have given the previous teachers info about CF and they have placed it into a folder and have passed it down every year so far.
I also tlaked to the NEW principal when i dropped Austin off at summer school and she said in all her years she has not EVER had one child with Cysitc Fibrosis. So I guess it would be time to educate her also.
Any suggestions are welcome!