Guest guest Posted July 26, 2004 Report Share Posted July 26, 2004 wow Judie! It sounds like shes doing AMAZINGLY! She might get a kick out of the group that's been set up for the young adults with MDS to chat!! It's amazing that you didn't find out until recently that she's mosaic... Well, I'm Angel, and from Southern CA... also the mother of 6 children! We have 5 boys and 1 girl! is our 3rd child. No one noticed his Downs at birth, althought *I* thought he looked VERY different from the other children. What we had an immediate issue with was his bowel disease, he wasn't able to pass any AT ALL, and had to have a colostomy at 3 days old. Had a couple more operations by the time he was 6 months old. Thankfully he's been quite healthy since then. 's MDS was diagnosed at 16 mos, when I was pregnant again, and just happened to take with me to my appt with a geneticist to talk about the bowel disease being passed on to the other kids... she spent more time staring at him than talking to me, and finally asked if she could do HIS bloodwork! 2 weeks later we had a diagnosis of MDS...but we weren't shocked at all...we knew something was wrong, but couldnt get the dr's to listen to us over the months. He's 11 now... we're just facing puberty... he's about to start 6th grade, and is in a severly handicapped class. Next week he has an appt for some evaluations at Kaiser, because his teacher feels very strongly that something ELSE is keeping him from learning... very possibly, ADD, and possibly dyslexia...but this appt will be a long one to screen for everything! I'm looking forward to that....he's been at an academic standstill for YEARS now. Sigh... It's great to hear about your daughter and how amazingly she's doing!! ~ANGEL~ Mom to 11 Mosaic Down Syndrome/Hirschsprung's Disease Lance 15, Tyler 12, 9 Jaeda 8 & Shayne 2 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2004 Report Share Posted July 27, 2004 Wow Judie - Your daughter sounds like an awesome young women, who had wonderful parents to guide her along the way. Your story is an inspiration to those of us who are just beginning this journey with our babies. My grandson Adam has MDS. He was diagnosed at 2 days old. He just turned two a couple of weeks ago. I am happy to say he is progressing wonderfully and has had no major health problems. I was fortunate to be blessed again with a granddaughter six weeks after Adam was born. She will be two in a couple of weeks. Now we have started to notice something that I find amazing. Skylar (my granddaughter) has taken over as teacher. She likes to be in charge, so it comes easy to her. lol Adam has begin to copy whatever she does. If she runs, he runs. She learned to climb up on the couch and so he followed her up there. If he stand up on the couch she will tell him No No Sit. Today she stood and he looked right at her an told her to Sit. Adam has several therapist and they do a wonderful job with him, but I think he learns more from this tiny little girl. One funny story. The latest is she taught Adam how to turn on the stereo. I went into the kitchen for one minute, the stereo came on - full blast - and the two of them are in the middle of the living room dancing. It was so cute, we couldn't get mad. Donna - gram to Double Trouble - Adam 2 yrs mds and Sky 23 months -- 25 Years: Ups and Downs Dear moderator et al, Ups and Downs is the book I am slowly writing which I will never finish, because Christi will never be " finished. " I have 25 years' experience, specializing in inclusive education, which I am always happy to share. We only learned of her mosaicism last winter when she was unsuccessfully considered for enrollment in the Aricept trial at Stanford. Christi was born Christmas Day, 1978, and is the youngest of our six children, as well as the favorite aunt to our 19 grandchildren. Her patron saint is St. the Astonishing, which may explain why she is quite typical of a person who has Down syndrome, and that she is, well, astonishing in that she has outperformed her IQ. She has a high school diploma (regular curriculum, modified expectations, passed all competencies), a California driver's license, and a 4.0 gpa for 34 units of junior college classes, where she is a TA for the beginning Drama section. This fall she is enrolled in Dance Choreography and Auditioning Techniques. She loves Pilates and weight training, and plays skills golf for Special Olympics. She was blessed with a father who wholeheartedly supports my tenacious advocacy (her first IEP went to due process, and it pretty much continued that way), and an elementary school special educator who remains our friend, intimately involved to this day, long after teaching Christi to read and write cursive and pass the high school math competencies, and who always reassured me that I was not crazy to want her, for example, to take Spanish or economics or speak at graduation ceremonies, or take seven years to learn to drive. She never believed in plateaus, even when it was the expected norm for special education. Christi barely survived two cardiac repair surgeries in her second year of life, and is left with a faulty mitral valve which will eventually fail her. Now, she is surviving a broken engagement, a love affair the end of which truly broke her heart. It was Romeo and t With Down Syndrome, but even in pieces her heart is huge. So is her stomach, which never feels full and leaves her in a constant battle (mostly with me) against weight gain. She can count up a day's carbs and calories in her head, and calculate the daily average for a week, but she can't figure out why she doesn't lose weight when she cheats and doesn't count it (how normal is that?!). She keeps information in her Palm device, programs her VCR, and communicates with me largely by text messages from her studio apartment (a part of our home), but left to her own devices she would eat in front of the television all day. I distract her with weekly sewing lessons, art lessons, a special recreation bowling league, and volunteer work at the hospital. To find her the right job, I will probably have to develop yet another career for this now senior-citizen-mother and become a job developer... She's pictured on the July 2004 NDSS convention brochure (second from the top), and last August she was thrilled to be elected by her peers to the board of directors of the NDSC. At their convention in August, she's leading a self-advocate's workshop where she'll teach a hip hop dance routine, I hope! Maybe we'll meet some of you there; that would be wonderful! Judie Hockel Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2004 Report Share Posted July 27, 2004 Thanks for the encouragement and sharing your story. We've got a long road here, but encouraging to know that it isn't going to be too bad with a little patience!! Irene mom to Nat 10MDS, Luke 8, Emilia 5, Lilly 3 and Isaac 6mo jhockel@... wrote: Dear moderator et al, Ups and Downs is the book I am slowly writing which I will never finish, because Christi will never be " finished. " I have 25 years' experience, specializing in inclusive education, which I am always happy to share. We only learned of her mosaicism last winter when she was unsuccessfully considered for enrollment in the Aricept trial at Stanford. Christi was born Christmas Day, 1978, and is the youngest of our six children, as well as the favorite aunt to our 19 grandchildren. Her patron saint is St. the Astonishing, which may explain why she is quite typical of a person who has Down syndrome, and that she is, well, astonishing in that she has outperformed her IQ. She has a high school diploma (regular curriculum, modified expectations, passed all competencies), a California driver's license, and a 4.0 gpa for 34 units of junior college classes, where she is a TA for the beginning Drama section. This fall she is enrolled in Dance Choreography and Auditioning Techniques. She loves Pilates and weight training, and plays skills golf for Special Olympics. She was blessed with a father who wholeheartedly supports my tenacious advocacy (her first IEP went to due process, and it pretty much continued that way), and an elementary school special educator who remains our friend, intimately involved to this day, long after teaching Christi to read and write cursive and pass the high school math competencies, and who always reassured me that I was not crazy to want her, for example, to take Spanish or economics or speak at graduation ceremonies, or take seven years to learn to drive. She never believed in plateaus, even when it was the expected norm for special education. Christi barely survived two cardiac repair surgeries in her second year of life, and is left with a faulty mitral valve which will eventually fail her. Now, she is surviving a broken engagement, a love affair the end of which truly broke her heart. It was Romeo and t With Down Syndrome, but even in pieces her heart is huge. So is her stomach, which never feels full and leaves her in a constant battle (mostly with me) against weight gain. She can count up a day's carbs and calories in her head, and calculate the daily average for a week, but she can't figure out why she doesn't lose weight when she cheats and doesn't count it (how normal is that?!). She keeps information in her Palm device, programs her VCR, and communicates with me largely by text messages from her studio apartment (a part of our home), but left to her own devices she would eat in front of the television all day. I distract her with weekly sewing lessons, art lessons, a special recreation bowling league, and volunteer work at the hospital. To find her the right job, I will probably have to develop yet another career for this now senior-citizen-mother and become a job developer... She's pictured on the July 2004 NDSS convention brochure (second from the top), and last August she was thrilled to be elected by her peers to the board of directors of the NDSC. At their convention in August, she's leading a self-advocate's workshop where she'll teach a hip hop dance routine, I hope! Maybe we'll meet some of you there; that would be wonderful! Judie Hockel Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2004 Report Share Posted July 29, 2004 Dear Judie, Thanks for letting us know more about Christi and your family. I have to ask, why Christi was denied on the Aricept study? We have a member who was a part of the Aricept study. Please let us know how the convention goes with Christi and her teaching! It sounds very exciting and perhaps we will see you at our next convention next year! Kristy Colvin IMDSA President jhockel@... wrote: Dear moderator et al, Ups and Downs is the book I am slowly writing which I will never finish, because Christi will never be " finished. " I have 25 years' experience, specializing in inclusive education, which I am always happy to share. We only learned of her mosaicism last winter when she was unsuccessfully considered for enrollment in the Aricept trial at Stanford. Christi was born Christmas Day, 1978, and is the youngest of our six children, as well as the favorite aunt to our 19 grandchildren. Her patron saint is St. the Astonishing, which may explain why she is quite typical of a person who has Down syndrome, and that she is, well, astonishing in that she has outperformed her IQ. She has a high school diploma (regular curriculum, modified expectations, passed all competencies), a California driver's license, and a 4.0 gpa for 34 units of junior college classes, where she is a TA for the beginning Drama section. This fall she is enrolled in Dance Choreography and Auditioning Techniques. She loves Pilates and weight training, and plays skills golf for Special Olympics. She was blessed with a father who wholeheartedly supports my tenacious advocacy (her first IEP went to due process, and it pretty much continued that way), and an elementary school special educator who remains our friend, intimately involved to this day, long after teaching Christi to read and write cursive and pass the high school math competencies, and who always reassured me that I was not crazy to want her, for example, to take Spanish or economics or speak at graduation ceremonies, or take seven years to learn to drive. She never believed in plateaus, even when it was the expected norm for special education. Christi barely survived two cardiac repair surgeries in her second year of life, and is left with a faulty mitral valve which will eventually fail her. Now, she is surviving a broken engagement, a love affair the end of which truly broke her heart. It was Romeo and t With Down Syndrome, but even in pieces her heart is huge. So is her stomach, which never feels full and leaves her in a constant battle (mostly with me) against weight gain. She can count up a day's carbs and calories in her head, and calculate the daily average for a week, but she can't figure out why she doesn't lose weight when she cheats and doesn't count it (how normal is that?!). She keeps information in her Palm device, programs her VCR, and communicates with me largely by text messages from her studio apartment (a part of our home), but left to her own devices she would eat in front of the television all day. I distract her with weekly sewing lessons, art lessons, a special recreation bowling league, and volunteer work at the hospital. To find her the right job, I will probably have to develop yet another career for this now senior-citizen-mother and become a job developer... She's pictured on the July 2004 NDSS convention brochure (second from the top), and last August she was thrilled to be elected by her peers to the board of directors of the NDSC. At their convention in August, she's leading a self-advocate's workshop where she'll teach a hip hop dance routine, I hope! Maybe we'll meet some of you there; that would be wonderful! Judie Hockel Quote Link to comment Share on other sites More sharing options...
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