This is my first class photo, taken at Carnival when we were disguised and about to party on down. In total recognition of my regal status, note how we are all dressed up as Princes and Princesses ! We made the outfits ourselves, and I was so proud of mine I refused to wear anything else for days!
See "Lally" sat next to me there? Her real name is Sandrine, but I like to call her Lally. We love each other very much - she is dead groovy. She is my special person who looks after me, stays by my side at all times and helps me to learn.
Don't you just love this photo? Mama is in extasy here!
Oh - and good news! Yesterday Mama met with my 'educational team' (social services, headmistress, teacher, Sandrine, my 'educatrice' from my special centre I go to twice a week, and Mama) to assess how I am doing at school and discuss the way forward.
The social services told Mama that, since the law was passed in France in 2005 making it mandatory for special needs children to have the opportunity go to school with their peers, Princess Abigail is the first case of total success and no difficulty. The lady added that it was heart-warming to see how happy I was to go to school, how easily I have made friends, how naturally I have adapted to social rules and learning processes - and that whilst I have some real learning difficulties, I have generated so much joy and happiness. Mama was in tears she was so happy!
So the bottom line is : we are increasing my attendance to an extra half day, so nowI will be going to school on Tuesdays, Thursdays and Fridays! Am I a grown-up or WHAT?
Gosh, how I love that lucky star which watches over me so well!
The secret diary of Abigail, a young Franco-British Princess who is partial to sharing the life and times of her brothers William (14) and Nathan (12), her cousins Lena and Tess, and occasionally of her Mama and Papa too.
Abigail’s blog began in 2007 initially to replace the family photo album tradition but over the years has become her fun place to make friends with bloggers worldwide, and to share experiences with parents of fellow children with rare chromosome disorders.