Written on
August 6, 2011 by
Tammie
I know what your thinking…NEW SCHOOL YEAR? How many days till school starts??? I have a friend that started counting the minute summer started. I enjoy our homeschooling time together. I love the beginning of a new year…the goals for the year, the dreams of what you want to work on, the reality of what…
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in
Assitive Technology,
Cerebral Palsy,
Communication,
Day In And Day Out,
Dealing With Public Perceptions,
Education,
Family Life,
Fine Motor,
Gross Motor,
Homeschool,
Individual Educational Plans,
Learning Disabilities,
Occupational Therapy,
Physical Therapy,
Problem Solving,
Self Care,
Skill Development,
Social Skills,
Stress Relief,
Therapy
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Written on
July 23, 2011 by
Tammie
I don’t have to tell anyone, I don’t think, about how HOT it’s been this week. As I said before I’m a facebooker too, and sometimes my saturday posts get away from me, sorry. Some days blend into the next, but I digress. My father’s family has all kind of “drifted” apart (not saying that…
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So many times, as I’ve said before, we confuse the line between being ugly and being an advocate. Being an advocate is rooted in being educated–therefore, we are then prepared to educate others. Unfortunately, the loud, brash family is also going to get the attention (and they’ll do it claiming advocacy). This is not advancing…
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We’ve developed a really good system for getting the child to eat when we are together as a family. Like most things now that it has become the routine she doesn’t even need a lot of support for this most of the time, but occasionally she is too tired, anxious, excited, distracted, or angry to sit…
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Written on
May 26, 2011 by
Debbie
In my last post I mentioned how we use an iPod Touch to help Peanut communicate. Dana, a speech pathologist, asked me what apps we have found useful in helping Peanut with her communication. We have found a few apps that we like, but I thought it would be fun to see what everyone else…
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Written on
May 21, 2011 by
Tammie
What is it about the wheelchair that attracts people? Some times it’s the looks but other times there are full blown conversations with people the randomly say things (not all bad!) My first outing with my son and his wheelchair was to a restuarant. I was meeting a friend for breakfast. We were eating and…
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Written on
May 12, 2011 by
Debbie
This morning when I dropped Peanut off for school I realized I didn’t have her iPod Touch. She uses her iPod touch to communicate at school and over the last several months it has been a great way for her to participate in class. This isn’t the first time I have not had her “voice”…
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Written on
May 7, 2011 by
Tammie
You know who you are… your the mom that most can’t relate to, the mom that takes her job seriously. The mom that’s misunderstood more than understood. The one that stands up for what’s right and wrong. The one that is the child’s first teacher and strongest advocate. You are the REAL EXPERT of your child….
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Written on
May 5, 2011 by
Debbie
It is something we strive for when we have a child with special needs. We want the other children to treat our children as they would other friends. We want adults to have the same expectations as they would another child. We want our children to be included in the school classroom. I can’t count…
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Written on
May 2, 2011 by
Maggie
REGISTER NOW! MEET AND DISCUSS EDUCATIONAL ISSUES AND BEST PRACTICES WITH OTHER LOCAL MOTHERS OF CHILDREN WITH DOWN SYNDROME! 1-day Seminar THIS Friday, May 6 @ Queens College, Flushing, NY Meeting the Educational Needs of Children with Down Syndrome Amazing Opportunity to see Dr. Sue Buckley, Researcher with Down Syndrome Education International, present the best practices…
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