Where learning differences is understood and uniqueness is celebrated. Where we learn how to remediate the weakness and develop the strengths. Where support is a necessity, not a luxury.
Saturday, October 27, 2007
Teaching Multiplication Table the Visual Way, Trying Out Times Tales
I first heard about this TIMES TALES from CharlotteD at Learning Board. She highly recommended it. I don't know why I didn't get it sooner, but I wish I did. Another poster named "WishIknew" ordered it right away and here's what she said:
"I want to thank whoever it was that mentioned Times Tales for helping my son with multiplication. We got the flip charts yesterday and we've already learned 4 of the memory stories just messing around with the pictures. This kind of learning is SOOOO right for my son! He thinks it's silly, but fun. He starts third grade in a few weeks and hasn't even really started multiplication yet, but he thinks it's cool to have a fun story head start. Thank you, whoever you are!!!! (that whoever you are is CharlotteD:)
And so I ordered it and it arrived yesterday. I'm excited! We'll start working on it today :) I'll keep you posted on how it goes. By the way, the costumer sevice on that store is excellent!
Friday, October 26, 2007
Random Thoughts
How do I know when I am stressed? When I am waking up at 3 o'clock in the morning for a couple days and couldn't get myself to go back to sleep, then I know I am stressed. I love sleep, I enjoy sleep, but when sleep is hard to come, that means I am anxious.
I know I should be praying, and I will. I just want to type my random thoughts here, so I can jump start this blog.
I started this blog several months ago but wasn't really updating it as much as my personal mommy blog. But now that Schwablearning site is closing, I am determined to make this blog a haven to us parents of kids with LD.
So... I'm logging off to pray then will come back here tonight for a more informational post.
I know I should be praying, and I will. I just want to type my random thoughts here, so I can jump start this blog.
I started this blog several months ago but wasn't really updating it as much as my personal mommy blog. But now that Schwablearning site is closing, I am determined to make this blog a haven to us parents of kids with LD.
So... I'm logging off to pray then will come back here tonight for a more informational post.
Thursday, October 25, 2007
Stressed. Support Group About To Disintegrate? I Hope Not!
Remember this post? Well, it's a stressful time right now because that support group I was talking about is in the danger of "disintegrating". We received an announcement that the website is closing at the end of the year. The Schwabbies are still raising our hopes high. I guess it's kind of like "hoping against all hope". No definite news yet, but hopefully next week we'll hear of a plan. Till then, I will be posting most of my thoughts on LD here.
Saturday, September 15, 2007
Support Group
The other night we had one of those "Bad Night" at home, when from being a good afternoon, something happened and that something changed the dynamics of the night.
I almost blogged about it that night, but I knew I should not (and I'm glad I didn't). You see, had I posted that situation right away, I would have opened up "our family" to a lot of misunderstanding and misconception. In order to lessen those "misunderstanding, misconception or wrong perception", I would have to explain and give you (my dear reader and friends) the background of if all. But I was upset at that time, and I really didn't have the energy to type up a background story to vent. I needed to vent, I needed support, at that very moment.
And so I posted at Schwablearning Parent To Parent Message Board. I have been a member of that board for more than 3 years and so I have already developed "cyber friendships" there. It's a board for parents raising kids with Learning Disabilities, and so many of the parents there can truly understand, right away without me having to give a background, and without me having to explain in detail what the situation is. Many parents there can say "been there, done that, here's what you can do".
The point of this post is this: support groups are very important in our lives. VERY IMPORTANT. In whatever stage of life were in, we need a group of friends who can relate. Belongingness, closeness (with each other) and openness (allowing your self to be vulnerable) do not happen overnight, but you've got to start somewhere. It does not have to be a "cyber group". It could be a group at church, at school, at work, a formal AA group, a Mom's Playgroup, a marriage group, an exercise group, etc... The point in, we must invest time and effort to "belong" to a good support group.
Ahhh... there are so many things I want to share about the importance of a support groups. I don't think I can squeeze all my thoughts in this one post, so I'll stop for now and will do a part 2 sometime - sooner or later, most likely later :).
For more Works For Me Wednesday posts, visit the WFMW Hub at Rocks In My Dryer.
I almost blogged about it that night, but I knew I should not (and I'm glad I didn't). You see, had I posted that situation right away, I would have opened up "our family" to a lot of misunderstanding and misconception. In order to lessen those "misunderstanding, misconception or wrong perception", I would have to explain and give you (my dear reader and friends) the background of if all. But I was upset at that time, and I really didn't have the energy to type up a background story to vent. I needed to vent, I needed support, at that very moment.
And so I posted at Schwablearning Parent To Parent Message Board. I have been a member of that board for more than 3 years and so I have already developed "cyber friendships" there. It's a board for parents raising kids with Learning Disabilities, and so many of the parents there can truly understand, right away without me having to give a background, and without me having to explain in detail what the situation is. Many parents there can say "been there, done that, here's what you can do".
The point of this post is this: support groups are very important in our lives. VERY IMPORTANT. In whatever stage of life were in, we need a group of friends who can relate. Belongingness, closeness (with each other) and openness (allowing your self to be vulnerable) do not happen overnight, but you've got to start somewhere. It does not have to be a "cyber group". It could be a group at church, at school, at work, a formal AA group, a Mom's Playgroup, a marriage group, an exercise group, etc... The point in, we must invest time and effort to "belong" to a good support group.
Ahhh... there are so many things I want to share about the importance of a support groups. I don't think I can squeeze all my thoughts in this one post, so I'll stop for now and will do a part 2 sometime - sooner or later, most likely later :).
For more Works For Me Wednesday posts, visit the WFMW Hub at Rocks In My Dryer.
Friday, July 6, 2007
Others land on Holland, others land on Switzerland...
I just read this post below, posted by Neurotic Fitch Mom. I probably should just have linked there, but I think it's good to have the whole post here. I'll let her know I posted here. The title o this post is NORMAL:
"Imagine," she said, taking a seat next to me on the rickety playground bench. "You've decided to take a trip to New York City. You've packed your high heels and your best clothes and you're planning to hit the town and see all the shows. But you get off the plane and you're in Switzerland. It's a little colder, a little slower, but still nice. Just different. It's the same with these kids."
"I just wanted him to be normal," I replied, looking up to watch him and the other Fifth Graders running wildly over the wooden structures, her class in the mix.
"Whatever that means," she said.
I thought I'd reached the point where I wanted to know, even if I didn't like the answer. I'd put it off for years, even though some part of me knew he was different from the start.
He spoke young, Daddy and Mama followed by thermostat and full sentences before he was one. At two he was flapping, little arms going like butterfly wings, close to his sides, lips buzzing. I thought he was pretending to fly. Until I noticed it more and more, when he was bored, when he was tired, when he was mad, when he was joyous.
"Are you an airplane or a helicopter," I asked him.
"Neither Mama."
At age four, his eyes huge and blue, never really looked at me. He gazed somewhere behind my head or turned his face entirely away.
"Don't you like Mama's face?" I teased him. "Am I that ugly?"
"You're beautiful Mama. I'd never think that," he replied, still not seeing me.
And then he went to school. Kindergarten, right across the street with a 1st year teacher. He brought home yellows and reds everyday and she made sure to meet me in the parent pickup line to list his transgressions.
"He's the sweetest thing but he goes on and on about Toy Story when I'm trying to teach. It's distracting the class."
Toy Story, which played constantly on one of the TVs at the house and had for almost two years. We had Toy Story bedding, dishes, toothpaste, clothes and toys. Just like the Thomas the Tank Engine phase we'd gone through two years before. I felt like I knew George Carlin and Buzz Lightyear personally.
"He's making these noises, humming and he's having meltdowns over the smallest things. But he's so smart."
"I'll talk to him," I'd assure her going home to cry. Beating myself up for not enrolling him in preschool. Not sure what the answer was myself.
Until 2nd grade, when a teacher's assistant pointed me to a website, that described my boy to a tee.
"He reminds me of my sister's boy," she said, handing me the slip of paper with a link.
But I still hesitated to make it official, to put what I saw as a stigma around his neck. Instead, I worked hard to give him coping techniques that didn't involve hour long sobs, to find out what set him off and teach him to cope.
In 4th grade, we'd meet an angel in pretty heels, his teacher, who two months in had him looking me in the eyes. Somehow she knew, but didn't say, rules and regulations keeping her from expressing her opinion.
"I taught him," she explained when I came to her with thankful tears. "I draw his eyes in with my finger and now he remembers."
He still had to think about it, eyes occasionally darting off, but it was a start. His meltdowns stopped other than a growl of aggravation every now and then, over intense stress. And I relaxed for awhile, until this year, 5th Grade, Junior high rapidly approaching.
I made an appointment.
4 hours later, leaving the office, Asperger's Syndrome, written down in the doctor's chicken scratch, my heart tearing apart.
"It's like teaching any other child math or reading," she told me as a tear rolled down my cheek. "With a little help, he'll be fine."
He may never be "normal", who really is anyway? But watching my precious boy, sweaty face beaming at me across the sandy playground, I knew I'd pick Switzerland over New York, any day....
"Imagine," she said, taking a seat next to me on the rickety playground bench. "You've decided to take a trip to New York City. You've packed your high heels and your best clothes and you're planning to hit the town and see all the shows. But you get off the plane and you're in Switzerland. It's a little colder, a little slower, but still nice. Just different. It's the same with these kids."
"I just wanted him to be normal," I replied, looking up to watch him and the other Fifth Graders running wildly over the wooden structures, her class in the mix.
"Whatever that means," she said.
I thought I'd reached the point where I wanted to know, even if I didn't like the answer. I'd put it off for years, even though some part of me knew he was different from the start.
He spoke young, Daddy and Mama followed by thermostat and full sentences before he was one. At two he was flapping, little arms going like butterfly wings, close to his sides, lips buzzing. I thought he was pretending to fly. Until I noticed it more and more, when he was bored, when he was tired, when he was mad, when he was joyous.
"Are you an airplane or a helicopter," I asked him.
"Neither Mama."
At age four, his eyes huge and blue, never really looked at me. He gazed somewhere behind my head or turned his face entirely away.
"Don't you like Mama's face?" I teased him. "Am I that ugly?"
"You're beautiful Mama. I'd never think that," he replied, still not seeing me.
And then he went to school. Kindergarten, right across the street with a 1st year teacher. He brought home yellows and reds everyday and she made sure to meet me in the parent pickup line to list his transgressions.
"He's the sweetest thing but he goes on and on about Toy Story when I'm trying to teach. It's distracting the class."
Toy Story, which played constantly on one of the TVs at the house and had for almost two years. We had Toy Story bedding, dishes, toothpaste, clothes and toys. Just like the Thomas the Tank Engine phase we'd gone through two years before. I felt like I knew George Carlin and Buzz Lightyear personally.
"He's making these noises, humming and he's having meltdowns over the smallest things. But he's so smart."
"I'll talk to him," I'd assure her going home to cry. Beating myself up for not enrolling him in preschool. Not sure what the answer was myself.
Until 2nd grade, when a teacher's assistant pointed me to a website, that described my boy to a tee.
"He reminds me of my sister's boy," she said, handing me the slip of paper with a link.
But I still hesitated to make it official, to put what I saw as a stigma around his neck. Instead, I worked hard to give him coping techniques that didn't involve hour long sobs, to find out what set him off and teach him to cope.
In 4th grade, we'd meet an angel in pretty heels, his teacher, who two months in had him looking me in the eyes. Somehow she knew, but didn't say, rules and regulations keeping her from expressing her opinion.
"I taught him," she explained when I came to her with thankful tears. "I draw his eyes in with my finger and now he remembers."
He still had to think about it, eyes occasionally darting off, but it was a start. His meltdowns stopped other than a growl of aggravation every now and then, over intense stress. And I relaxed for awhile, until this year, 5th Grade, Junior high rapidly approaching.
I made an appointment.
4 hours later, leaving the office, Asperger's Syndrome, written down in the doctor's chicken scratch, my heart tearing apart.
"It's like teaching any other child math or reading," she told me as a tear rolled down my cheek. "With a little help, he'll be fine."
He may never be "normal", who really is anyway? But watching my precious boy, sweaty face beaming at me across the sandy playground, I knew I'd pick Switzerland over New York, any day....
Sunday, July 1, 2007
Celebrating Holland - I'm home
Celebrating Holland - Im Home
by Cathy Anthony
This is a follow up Welcome to Holland, by Emily Perl Kingsley.
The original essay can be found at www.nas.com/downsyn/holland.html. Cathy Anthony is a parent, advocate and presently the executive director of the Family Support Institute in Vancouver, BC(www.familysupportbc.com).
I have been in Holland for over a decade now. It has become home. I have had time to catch my breath, to settle and adjust, to accept something different than I’d planned. I reflect back on those years of past when I had first landed in Holland. I remember clearly my shock, my fear, my anger,the pain and uncertainty. In those first few years, I tried to get back to Italy as planned, but Holland was where I was to stay.
Today, I can say how far I have come on this unexpected journey. I have learned so much more. But, this too has been a journey of time. I worked hard. I bought new guidebooks. I learned a new language and I slowly found my way around this new land. I have met others whose plans had changed like mine, and who could share my experience. We supported one another and some have become very special friends.
Some of these fellow travelers had been in Holland longer than I and were seasoned guides, assisting me along the way. Many have encouraged me. Many have taught me to open my eyes to the wonder and gifts to behold in this new land. I have discovered a community of caring.
Holland wasn’t so bad. I think that Holland is used to wayward travelers like me and grew to become a land of hospitality, reaching out to welcome, to assist and to support newcomers like me in this new land.
Over the years, I’ve wondered what life would have been like if I’d landed in Italy as planned. Would life have been easier? Would it have been as rewarding? Would I have learned some of the important lessons I hold today? Sure, this journey has been more challenging and at times I would (and still do) stomp my feet and cry out in frustration and protest. And, yes, Holland is slower paced than Italy and less flashy than Italy, but this too has been an unexpected gift. I have learned to slow down in ways too and look closer at things, with a new appreciation for the remarkable beauty of Holland with its tulips, windmills and Rembrandts. I have come to love Holland and call it Home.
I have become a world traveler and discovered that it doesn’t matter where you land. What’s more important is what you make of your journey and how you see and enjoy the very special, the very lovely, things that Holland, or any land, has to offer.
Yes, over a decade ago I landed in a place I hadn’t planned. Yet I am thankful, for this destination has been richer than I could have imagined!
Welcome To Holland by Emily Perl Kingsley
Photo from Pixelatestudios.com
WELCOME TO HOLLAND
When I had my son, I knew he was going to be a hockey star... a jock, one of the popular kids, and smart. He was going to eat his vegetables too and brush his teeth without me even asking/telling. I have all that in my daughter... all of it, but with my son I have the complete opposite.
My son has Asperger's Syndrome. He's extremely bright, but hugely lacking in social skills. He has a very awkward gait and tires easily, so hockey, or being a jock - not happening with this kid. The popularity wasn't happening either, because of his inability to read nonverbal cues. On top of that, "many things" he did was misunderstood by his teachers. He brought a gift in for his pregnant teacher, and was bringing it back to his desk to put a chocolate kiss on it and she wigged out. and was furious with him - and took his good intentions and made it a bad thing. I explained his intentions to her but by that time i wanted to take the gift back and give her nothing myself! - how can teachers, who spend time with kids be so clueless about kids?
Right around the time we were trying to get James diagnosed, someone sent me a copy of Welcome to Holland. I copied it, shared it, saved it, and i read it OFTEN. To this day, 6 years after my son's diagnosis - i'm still hugely inspired.
I am truly, truly blessed - because i have both - my trip to italy: my daughter; and my trip to Holland: my son - "a little jetlagged"... :). Here's a copy of that Welcome to Holland...I hope it'll encourage another parent as it has encouraged me:
My son has Asperger's Syndrome. He's extremely bright, but hugely lacking in social skills. He has a very awkward gait and tires easily, so hockey, or being a jock - not happening with this kid. The popularity wasn't happening either, because of his inability to read nonverbal cues. On top of that, "many things" he did was misunderstood by his teachers. He brought a gift in for his pregnant teacher, and was bringing it back to his desk to put a chocolate kiss on it and she wigged out. and was furious with him - and took his good intentions and made it a bad thing. I explained his intentions to her but by that time i wanted to take the gift back and give her nothing myself! - how can teachers, who spend time with kids be so clueless about kids?
Right around the time we were trying to get James diagnosed, someone sent me a copy of Welcome to Holland. I copied it, shared it, saved it, and i read it OFTEN. To this day, 6 years after my son's diagnosis - i'm still hugely inspired.
I am truly, truly blessed - because i have both - my trip to italy: my daughter; and my trip to Holland: my son - "a little jetlagged"... :). Here's a copy of that Welcome to Holland...I hope it'll encourage another parent as it has encouraged me:
WELCOME TO HOLLAND
by Emily Perl Kingsley
©©1987 by Emily Perl Kingsley.
All rights reserved
I am often asked to describe
the experience of raising a child with a disability
to try to help people who have not shared
that unique experience to understand it,
to imagine how it would feel.
It's like this......
When you're going to have a baby,
it's like planning a fabulous vacation trip - to Italy.
You buy a bunch of guide books and make your wonderful plans.
The Coliseum. The Michelangelo David. The gondolas in Venice.
You may learn some handy phrases in Italian. It's all very exciting.
After months of eager anticipation, the day finally arrives.
You pack your bags and off you go.
Several hours later, the plane lands.
The stewardess comes in and says,
"Welcome to Holland."
"Holland?!?" you say. "What do you mean Holland??
I signed up for Italy! I'm supposed to be in Italy.
All my life I've dreamed of going to Italy."
But there's been a change in the flight plan.
They've landed in Holland and there you must stay.
The important thing is that they haven't taken you
to a horrible, disgusting, filthy place,
full ofpestilence, famine and disease.
It's just a different place.
So you must go out and buy new guide books.
And you must learn a whole new language.
And you will meet a whole new group of people
you would never have met.
It's just a different place.
It's slower-paced than Italy, less flashy than Italy.
But after you've been there for a while
and you catch your breath, you look around....
and you begin to notice that Holland has windmills....
and Holland has tulips.
Holland even has Rembrandts.
But everyone you know is busy coming and going from Italy...
and they're all bragging about
what a wonderful time they had there.
And for the rest of your life, you will say
"Yes, that's where I was supposed to go.
That's what I had planned."
And the pain of that will never, ever, ever, ever go away...
because the loss of that dream is a very very significant loss.
But... if you spend your life
mourning the fact that you didn't get to Italy,
you may never be free to
enjoy the very special, the very lovely things ...
about Holland.
******
the experience of raising a child with a disability
to try to help people who have not shared
that unique experience to understand it,
to imagine how it would feel.
It's like this......
When you're going to have a baby,
it's like planning a fabulous vacation trip - to Italy.
You buy a bunch of guide books and make your wonderful plans.
The Coliseum. The Michelangelo David. The gondolas in Venice.
You may learn some handy phrases in Italian. It's all very exciting.
After months of eager anticipation, the day finally arrives.
You pack your bags and off you go.
Several hours later, the plane lands.
The stewardess comes in and says,
"Welcome to Holland."
"Holland?!?" you say. "What do you mean Holland??
I signed up for Italy! I'm supposed to be in Italy.
All my life I've dreamed of going to Italy."
But there's been a change in the flight plan.
They've landed in Holland and there you must stay.
The important thing is that they haven't taken you
to a horrible, disgusting, filthy place,
full ofpestilence, famine and disease.
It's just a different place.
So you must go out and buy new guide books.
And you must learn a whole new language.
And you will meet a whole new group of people
you would never have met.
It's just a different place.
It's slower-paced than Italy, less flashy than Italy.
But after you've been there for a while
and you catch your breath, you look around....
and you begin to notice that Holland has windmills....
and Holland has tulips.
Holland even has Rembrandts.
But everyone you know is busy coming and going from Italy...
and they're all bragging about
what a wonderful time they had there.
And for the rest of your life, you will say
"Yes, that's where I was supposed to go.
That's what I had planned."
And the pain of that will never, ever, ever, ever go away...
because the loss of that dream is a very very significant loss.
But... if you spend your life
mourning the fact that you didn't get to Italy,
you may never be free to
enjoy the very special, the very lovely things ...
about Holland.
******
Saturday, June 9, 2007
Summer Kit
I just discovered this "Summer Planning 2007" article at Schwablearning. I think it's very helpful to all parents (not only the ones who has kids with learning differences, but for everyone) so I'm sharing this. Go there to see for yourself. And while you're there, check out their Summer Read Along program too.
Wednesday, May 16, 2007
Rick Lavoie - Helping Kids with Learning Differences
If you have a child who at one point is struggling in school...I recommend you check out one or all of these videos (or DVD) by Rick Lavoie. The descriptions of each DVD or videos can be read HERE. Read more about these on Rick Lavoie's website. Each child is unique and special and they should not struggle in school. I guarantee you, these videos work! It worked with US :). It will inform you and empower you to be a great advocate for your child. Check them out:
Saturday, February 10, 2007
Posts from My Other Blog
If you came here from a place other than my other blog LIZA'S EYEVIEW, then you haven't read my posts there yet about LD related issues and stuff. I posted them there before I decided to start a blog specific to LD. So here's the link to those posts: CLICK HERE
I will probably repost some of it here later..but for now, please go there and check it out.
I will probably repost some of it here later..but for now, please go there and check it out.
The Blog Plan
If you visited this site ... i am assuming you're interested in this topic.
Please keep on coming back because this site will be full of resources that will help you parent your child with learning disabilities. In fact if you're the one with LD, this will tremendously help you too.
I'm just a little overwhelmed with the many things i need to do..but believe me - this blog will be one of the best blog on LD :)
I will Feature:
1. Reviews of best Books on helping kids with LD
2. Reviews on best books for LD kids (oh, you'd love these)
3. Recommended DVD's (Teaching and LD related) - My favorite is Rick Lavoie and that will be my first review. Watch for it!
4. And more!!!!
Please keep on coming back because this site will be full of resources that will help you parent your child with learning disabilities. In fact if you're the one with LD, this will tremendously help you too.
I'm just a little overwhelmed with the many things i need to do..but believe me - this blog will be one of the best blog on LD :)
I will Feature:
1. Reviews of best Books on helping kids with LD
2. Reviews on best books for LD kids (oh, you'd love these)
3. Recommended DVD's (Teaching and LD related) - My favorite is Rick Lavoie and that will be my first review. Watch for it!
4. And more!!!!
Sunday, February 4, 2007
I'm stuck!
So much to do...so little time...
1. Get legal paperwork - non-profit status (a friend lawyer already said he'd have his office assist me - for free!)
2. Learn how to apply for grants (maybe K from Schwab can help?)
3. Write Objectives, Goals, etc.
3. Write Grant Application
In the meantime (while waiting to do the above)
1. Create a blog (I need technical support!)
2. Maintain Blog (I need help with blogging)
3. Find Blog Sponsors
4. Advertise Blog
5. Hold Workshops
1. Get legal paperwork - non-profit status (a friend lawyer already said he'd have his office assist me - for free!)
2. Learn how to apply for grants (maybe K from Schwab can help?)
3. Write Objectives, Goals, etc.
3. Write Grant Application
In the meantime (while waiting to do the above)
1. Create a blog (I need technical support!)
2. Maintain Blog (I need help with blogging)
3. Find Blog Sponsors
4. Advertise Blog
5. Hold Workshops
Friday, January 5, 2007
Passion or Obsession
This was originally posted at Schwablearning Parent to Parent Message Board on 5/12/04. I thought it would be appropriate to use this as my intro and trial post. Here it goes:
Lately, I have been noticing how consumed I am about researching, learning and talking about learning disabilities, specially with regards to my son.
The other day, as I sat at a T-ball game, one of the parents asked...how's G (my son) doing? My response was "Oh he's doing a lot better!". Then she asked, "why, was he sick?" I suddenly realized that she was just asking a casual "how are you" and there I was ready to explain how G's tutoring and med has tremendously helped him in school, and how his behavior is improving.
The other night when I found a time to watch a DVD/VHS of my choice to relax...I found my self choosing to watch Rick Lavoie's videos. Mind you, I've watched these at least 5 times already and yet given the choice, I chose to watch it over the commercial DVD's we have. And guess what? I still thoroughly enjoyed it as I learn new things and got reminded of the techniques I am slowly forgetting.
Eventhough I already am a very busy mom and wife, I still chose to put together a workshop for the parents of kids with learning disability. I got very excited when I a few parents signed-up already when I haven't even fully advertised it.
I spend most of my free time reading and researching about LD and stories of people with LD. When I go to the bookstore, most of the time I go straight to the Special Education section. The thing is, I am enjoying this. I don't feel it's a burden at all. Am I getting obsessed with this? Ahh...I think I am not. I believe this is PASSION, NOT OBSESSION. The same passion that drove Jesus to the cross because of his love for us, is the same passion that I have about helping my learning disabled son (to those with different religious belief, pardon me for the religious analogy, I can’t help it as it’s a personal conviction of mine).
Anyone has a dictionary? I can't find mine :)
Lately, I have been noticing how consumed I am about researching, learning and talking about learning disabilities, specially with regards to my son.
The other day, as I sat at a T-ball game, one of the parents asked...how's G (my son) doing? My response was "Oh he's doing a lot better!". Then she asked, "why, was he sick?" I suddenly realized that she was just asking a casual "how are you" and there I was ready to explain how G's tutoring and med has tremendously helped him in school, and how his behavior is improving.
The other night when I found a time to watch a DVD/VHS of my choice to relax...I found my self choosing to watch Rick Lavoie's videos. Mind you, I've watched these at least 5 times already and yet given the choice, I chose to watch it over the commercial DVD's we have. And guess what? I still thoroughly enjoyed it as I learn new things and got reminded of the techniques I am slowly forgetting.
Eventhough I already am a very busy mom and wife, I still chose to put together a workshop for the parents of kids with learning disability. I got very excited when I a few parents signed-up already when I haven't even fully advertised it.
I spend most of my free time reading and researching about LD and stories of people with LD. When I go to the bookstore, most of the time I go straight to the Special Education section. The thing is, I am enjoying this. I don't feel it's a burden at all. Am I getting obsessed with this? Ahh...I think I am not. I believe this is PASSION, NOT OBSESSION. The same passion that drove Jesus to the cross because of his love for us, is the same passion that I have about helping my learning disabled son (to those with different religious belief, pardon me for the religious analogy, I can’t help it as it’s a personal conviction of mine).
Anyone has a dictionary? I can't find mine :)
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