Jaynine

My daughter is now 30 years old. She lives with 6 friends in a Residential Home.
Life has always been a roller coaster ride with my girl but each little achievement puts me on a high for months. Her smile lights up a room and brings such happiness into your heart that life would be very dull without her. I have always thought myself lucky that Jaynine always appeared to be in the middle of the aicardi spectrum, possibly leaning to the stronger side. She was diagnosed at 6 weeks old, did'nt walk until about 5 and then lost that ability again about 12 and is now vertually wheelchair bound. She needs 24 hour care for all personal needs. She has a wicked no perhaps warped sense of humour is more accurate. She is able to label some items but cannot hold a conversation. That is all for now.