We played with Hughan’s Duplo circus set.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
Hughan is still saying “more” for his tea, when he has finished drinking his first mug in the morning.
School again! A train went past at the back of the play school, the children all went crazy and wanted to be picked up to see it go past. Hughan thought it was great.
Jamie played with Hughan and his train set in the afternoon.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
When Hughan had finished his tea this morning he said what sounded like “more!” Willem couldn’t believe his ears.
We all showed him this was great and Hughan was very pleased with himself when Willem produced more tea.
We went to play school in the morning. Hughan joined in with the children again today and he has started vocalising well with the other children. He is fitting in really well and enjoying play school.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
Hughan had a great time with Willem blowing out the flames on his lighter. He has started blowing well.
We visited friends in the afternoon.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
Hughan and I went to play school again today. The play school have been given some little cars for the children. Hughan enjoyed playing with them
We went to the farm in the afternoon.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
Hughan helps push the coffee table into place and automatically sets off for his little chair, which is in the bedroom.
I find his best time of the day is straight after breakfast, he has the best attention then.
Today we played with puzzles and matching colours.
Jamie’s sports day. Hughan went in the young brothers race.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
We spent most of the day on the road, taking Willem’s Mum (Granny Dawn) back to Mafeking.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
Over the weekend we went through to Mafeking to see Willem’s family. His sister has just had a baby, a little boy that they have called Shaun.
Hughan loved the baby, his cousin. Granny was also there from Zimbabwe, so Jamie was very excited to see her again.
Granny has a hearing problem so she feels very close to Hughan. We brought her back to Gaborone with us for the weekend.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
Play school again. Hughan makes such lovely noises in the car on our way to play school. Every morning he points to his schoolbag and pulls at the handle and talks away.
I know exactly what he wants, he wants to go to school.
His Play School Teacher mentioned today how she had noticed he is venturing off by himself. I always stay with him for the session.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)
I have started moving the coffee table, that is in the centre of the lounge, near the one large window in the lounge.
Hughan gets his little chair from the bedroom and puts it at the table. I sit on the carpet and face the light (window).
Our main topic today was the Lego. We made a house, a car and played with the Lego playground set. Hughan is vocalising well.
(I started this website to help other patents with deaf children through our experience. Our son Hughan was born in 1988 and was diagnosed profoundly deaf at 14 months old. We kept a Diary, so his progress could be tracked between our lessons, as we were living in Gaborone in Botswana and traveled every 3 months to the Carel du Toit Centre in Cape Town.)