There have been a few comments on the other blogs that Jill is no longer around. Any truth to that? Did she run away and if so, did she take Trig with her?
Showing posts with label Down Syndrome. Show all posts
Showing posts with label Down Syndrome. Show all posts
Is Jill Palin still around?
There have been a few comments on the other blogs that Jill is no longer around. Any truth to that? Did she run away and if so, did she take Trig with her?
Is Sarah Palin hoping Trig only makes it to 20?
From Hoohah's Fecebook page
Enjoy this beautiful greeting from father to son.
http://www.patheos.com/blogs/bristolpalin/2012/05/living-life-well-for-40-years-and-counting/
I read it again yesterday while waiting for Trig to awaken after eye surgery. So groggy from deep sleep at the hands of a skilled anesthesiologist, our son's surgeon also waited and reassured. And he told me the most fascinating thing about the eyes of a child with Down syndrome. "Compare his eyes to a 'normal' child's. Get a magnifying glass. Look deep. Their eyes are captivating inside! They're different, they're colorful, they sparkle. Surely God made these eyes to reflect what heaven must be."
If only we all could see into and through the eyes of the innocent! They're God's sons and daughters who may not meet man's standards of perfection but will certainly meet His. Their enduring childlike faith and their patience with the rest of us can teach us what is important. Maybe if we look with those eyes, what a wonderful world we will see.
- Sarah Palin
So many things wrong with this.
The average lifespan for a Down Syndrome person is between 55-60. Not 40. and certainly not 20. But the way Sarah has treated Trig, he may only make it to 20, which is probably what she really wants as she cannot stand the boy and is no longer of any use to her.
I am sure George Will, as much as I disagree with him, is a loving father who saw to it that Jon got therapy and good care so he could have a normal life, which is something Hoohah hasn't done with Trig.
Even though I have a belief in God, he doesn't not magically point at something and poof makes it better. When I was growing up my grandma got this cross-stitch picture for Mother's Day that said "God can't be everywhere so he invented mothers", she hung it in her kitchen. Same thing here, God created doctors and therapists to take care of us here on earth. If you disagree with me on that that's OK, but that is my take on it. God put people on earth to do his work.
And for a little snark, look at the picture of Jon with Dumbya. Even with Down Syndrome I am sure Jon is much more intelligent than Dumbya. Sorry but I had to say it.
Today is the last day of October and Sarah Palin still has not made any comment about October being Down Syndrome month
In fact for the entire month of October this all she posted regarding Down Syndrome:
One of the "good guys" in the media forwarded this, knowing it would make my day, as I hope it does yours! (Thank you, Kate O'Hare, for being part of the good stuff in today's print, TV and internet mediums!) Friends, please watch this short video that exudes joy, right priorities, and God's gifts that come in all sorts of beautiful expression. Enjoy!
And now I'm headed over to Todd's airplane hanger to ready for a Sean Hannity interview for his FOX show tonight!
- Sarah Palin
http://www.myfoxtwincities.com/story/26807899/down-syndrome-dancer-reminds-instructor-what-dance-is-all-about
And it wasn't until October 21 the day the brawl tapes were released.
October is National Downs Syndrome month
From the Down Syndrome of Greater St. Louis
Down Syndrome Awareness Month is chance to spread awareness, advocacy and inclusion throughout the community. During the month of October, we celebrate individuals with Down syndrome and make people aware of their abilities and accomplishments. And we have friends everywhere helping spread the word -thanks to St. Louis Mayor Francis Slay and Missouri Governor Jay Nixon officially proclaiming October as Down Syndrome Awareness Month.
So is Skanky going to honor Trig or do anything to promote and educate people about Down Syndrome? I think not.
BTW who was watching Trig the night of the brawl?
As expected Sarah Palin makes an ass out of herself in Joplin
From The Joplin Globe
When Sarah Palin was told her child would have Down syndrome, her doctor gave her a book. But Palin couldn’t open it because she wasn’t sure she was equipped to handle it.
She remembered asking her husband, “Why us?”
His response: “Why not us?”
Palin spoke Thursday night to a filled Taylor Performing Arts Center on the Missouri Southern State University campus. Her talk was part of an informational and fundraising event for LifeChoices Health Network, which spent the night marking its 25th anniversary.
Mixing her talk with jokes, her political thoughts and various anecdotes, the former Alaskan governor and vice presidential nominee spoke about having a child with Down syndrome, as well as about her daughter Bristol’s pregnancy.
“It’s not a story; it’s a chapter of my life,” she said.
She reflected on being 12 weeks pregnant and having an ultrasound when the technician told her the baby’s neck was a bit thicker than normal. At the time, Palin was told there was a good chance things would be just fine.
Later, however, when the doctor performed more tests, Palin found out her child would have Down syndrome.
At the time, she wasn’t sure she could handle it, she said. She was busy being the governor, chairing a board and taking care of four other children. About that time, her daughter Bristol announced that she was pregnant.
I think I will spare all of you and now post any video. I just watched it and now I have a headache.
My apologies to the newest member of the Palin family
From Sarah's Fecebook page:
Happy household this weekend as we welcomed a new addition to our family! Our new four-legged love, Jill Hadassah, comes to us with great training under her collar by our friend in Iowa Becky Beach and her Puppy Jake Foundation, along with Canine Craze in Des Moines. The Puppy Jake charity trains dogs for adoption by our service men and women, including those recovering from PTSD, as well as families with special needs. Jill Hadassah has been trained to be Trig’s buddy, and we’re over the moon to finally have her home! Thrilled, too, because all the rescue dogs and cats our kids have adopted over the years will hopefully learn something from our first dog trained to do anything! She’s brilliant and beautiful, and we feel very blessed to have her.
Thank you so much, Becky and Puppy Jake Foundation, for working with this tail-wagging bundle of love. We’ll treasure her, as she joins the rest of the current furry members of our family: Lucy, Lola, and Wilson.
Please visit the Puppy Jake Foundation to learn more about the great work they do, and join us in supporting them if you feel led to do so!
http://puppyjakefoundation.com/
https://www.facebook.com/PuppyJakeFoundation
Sarah if you had gotten Trig therapy earlier he may not need a dog now. You suck.
Jill I'm so sorry you were adopted by the Palins. I hope you can run away and take Trig with you. Even a dog can take better care of Trig than his "parents".
October was Down Syndrome Awareness Month, was Sarah even aware of that?
You can read more about Down Syndrome Awareness Month at National Down Syndrome Society website.
I don't think Sarah had a single Facebook post all month about Down Syndrome. I could be mistaken but all she did in October was insult President Obama and campaign for a loser candidate in Steve Lonegan. If she did say anything my mistake.
NDSS Your Way invites you to compete, celebrate and create with us through our online fundraising program that is geared towards independent fundraisers interested in raising money on behalf of NDSS. Down Syndrome Awareness Month is a great time to start! Through Team NDSS, NDSS Celebrations or NDSS New Ideas we invite you to have a bake sale, grow a mustache, run a marathon, throw a party, organize a bowl-a-thon - however you do it, do it for NDSS and do it Your Way! - See more at: http://www.ndss.org/About-NDSS/Newsroom/Recent-News/Down-Syndrome-Awareness-Month-2013/#sthash.z0gQ0PCW.dpuf
NDSS founded the Buddy Walk® in 1995 to spread our mission of promoting the value, acceptance and inclusion of people with Down syndrome at the local level. The National Buddy Walk® Program has grown from 17 Walks in 1995 to over 250 Buddy Walks expected this year. Last year, over 295,000 people participated in a Buddy Walk® and over $11.75 million was raised to support both local and national programs. Most Buddy Walks take place in and around October in celebration of Down Syndrome Awareness Month. - See more at: http://www.ndss.org/About-NDSS/Newsroom/Recent-News/Down-Syndrome-Awareness-Month-2013/#sthash.z0gQ0PCW.dpuf
NDSS founded the Buddy Walk® in 1995 to spread our mission of promoting the value, acceptance and inclusion of people with Down syndrome at the local level. The National Buddy Walk® Program has grown from 17 Walks in 1995 to over 250 Buddy Walks expected this year. Last year, over 295,000 people participated in a Buddy Walk® and over $11.75 million was raised to support both local and national programs. Most Buddy Walks take place in and around October in celebration of Down Syndrome Awareness Month. - See more at: http://www.ndss.org/About-NDSS/Newsroom/Recent-News/Down-Syndrome-Awareness-Month-2013/#sthash.z0gQ0PCW.dpuf
NDSS founded the Buddy Walk® in 1995 to spread our mission of promoting the value, acceptance and inclusion of people with Down syndrome at the local level. The National Buddy Walk® Program has grown from 17 Walks in 1995 to over 250 Buddy Walks expected this year. Last year, over 295,000 people participated in a Buddy Walk® and over $11.75 million was raised to support both local and national programs. Most Buddy Walks take place in and around October in celebration of Down Syndrome Awareness Month. - See more at: http://www.ndss.org/About-NDSS/Newsroom/Recent-News/Down-Syndrome-Awareness-Month-2013/#sthash.z0gQ0PCW.dpuf
Sarah Palin hasn't done shit for Down's Syndrome
Down's Syndrome Day was on March 21.
Not a Facebook post from Sarah
Not a tweet.
She never attended the convention either.
Shameful cuz her "son" has Down's Syndrome. Has she ever donated money to Down's Syndrome causes?
This is why I no longer read Newsweek
From The Daily Beast
Last week, Rick Santorum and his family offered us a reminder of what really matters. When his 3-year-old daughter, Bella, born with Trisomy 18, was hospitalized with pneumonia, Rick left the campaign trail to be by her bedside. In the middle of this very heated campaign season, many of us prayed through tears for Bella’s health and added prayers of thankfulness for a public example of someone’s sacrifice made with the right priorities.
It’s a sacrifice every parent and caregiver of a child with special needs sympathizes with. Families of children with special needs are bonded by a shared experience of the joys, challenges, fears, and blessings of raising these beautiful children whom we see as perfect in this imperfect world.
During the 2008 presidential campaign, on rope lines at rallies across the country, my husband, Todd, and I met so many of these families and caretakers, and I’ll never forget them. There was an instant connection—a kind of mutual acknowledgment that said, “Yes, these children are precious and loved. Yes, we face extra fears and challenges, but our children are a blessing, and the rest of the world is missing out in not knowing this.”
Every parent struggles with juggling the commitments of work and family. Women, especially, know this well. Over the years, I’ve learned that women can “have it all,” just not all at once. For me, it was a lesson learned through the school of hard knocks, but it was one my own mother made me aware of when she calmly told me that as a working mom in the rough-and-tumble political arena, I would have to make tough choices. We all do. In making decisions about my career, I’ve put my family first, and I’ve never regretted it, although it has meant periodically putting particular pursuits on the back burner.
When I discovered early in my pregnancy that my baby would be born with an extra chromosome, the diagnosis of Down syndrome frightened me so much that I dared not discuss my pregnancy for many months. All I could seem to muster was a calling out to God to prepare my heart for what was ahead. My prayers were answered beyond my shallow understanding of what true joy could be. Yes, raising a child with special needs is a unique challenge, and there’s still fear about my son Trig’s future because of health and social challenges; and certainly some days are much more difficult than if I had a “normal” child.
Many everyday activities like doctor’s appointments and social gatherings and travel accommodations and even mealtimes and a solid night of sleep are that much more difficult, but at the end of the day I wouldn’t trade the relative difficulties for any convenience or absence of fear. God knew what he was doing when he blessed us with Trig. We went from fear of the unknown to proudly displaying a bumper sticker sent to us that reads: “My kid has more chromosomes than your kid!” He may not be the next Wayne Gretzky, but our hearts are filled with so much pride watching Trig giggle with his sisters’ puppies, or sway to the rhythm of his Little Angels DVDs, it’s as if he were hoisting the Stanley Cup.
Granted, I know I may be more fortunate than others to have loving friends and a big, supportive family I call on to help, including a husband who spends many sleepless nights with this restless little one. (And Todd actually makes Trig’s puréed baby food!) Others aren’t so fortunate, and in our thankfulness I am made more compassionate toward others who have less.
I often think now, what would we do without Trig? He’s our “everything that really matters.”
Trig is almost 4 years old now, and every morning when he wakes up, he pulls himself up, rubs the sleep out of his eyes, looks around, and then starts applauding! He welcomes each day with thunderous applause and laughter. He looks around at creation and claps as if to say, “OK, world, what do you have for me today?”
My family knows that Trig will face struggles that few of us will ever have to endure, including people who can be so cruel to those not deemed “perfect” by society. The cruelty is more than made up for, though, when someone simply smiles at our son. Nothing makes me prouder. As I explained in a Thanksgiving article, I notice it happens often in airports. Travelers passing by will do a double-take when they see him, perhaps curious about the curious look on his face; or perhaps my son momentarily exercises an uncontrollable motion that takes the passerby by surprise. Perhaps, as an innocent and candid child announced when she first met Trig, they think, “He’s awkward.” But when that traveler pauses to look again and smiles, and maybe tells me what a handsome boy I have, I swell with pride. I am so thankful for their good hearts. They represent the best in our country, and their kindness shows the real hope we need today.
My family understands that up ahead, some days will be better than others. We will adapt and juggle things and work through it. But Trig applauds the day. And that’s what he teaches us. That’s our priority, and we’re blessed by it.
I smell bullshit on this one.
Todd still purees Trig's food? Trig should be able to eat solid foods by now. Even if he does have Down's. If he cannot eat solid food by now then Sarah and Todd have done a poor job in getting him developed.
Why has Sarah donated so little money to charities that specialize in Down's Syndrome?
I doubt Sarah and Todd take Trig anywhere, especially to airports. There has not been a public sighting of Trig in ages.
Trig looks way too much like Levi in this picture. Don't you think?
It's rich that Sarah blasts Newsweek for giving Andrew Sullivan any print but she will run to them so she can get sympathy. Guess she is really worried about Babygate being exposed and Game Change airing in a month.
Last week, Rick Santorum and his family offered us a reminder of what really matters. When his 3-year-old daughter, Bella, born with Trisomy 18, was hospitalized with pneumonia, Rick left the campaign trail to be by her bedside. In the middle of this very heated campaign season, many of us prayed through tears for Bella’s health and added prayers of thankfulness for a public example of someone’s sacrifice made with the right priorities.
It’s a sacrifice every parent and caregiver of a child with special needs sympathizes with. Families of children with special needs are bonded by a shared experience of the joys, challenges, fears, and blessings of raising these beautiful children whom we see as perfect in this imperfect world.
During the 2008 presidential campaign, on rope lines at rallies across the country, my husband, Todd, and I met so many of these families and caretakers, and I’ll never forget them. There was an instant connection—a kind of mutual acknowledgment that said, “Yes, these children are precious and loved. Yes, we face extra fears and challenges, but our children are a blessing, and the rest of the world is missing out in not knowing this.”
Every parent struggles with juggling the commitments of work and family. Women, especially, know this well. Over the years, I’ve learned that women can “have it all,” just not all at once. For me, it was a lesson learned through the school of hard knocks, but it was one my own mother made me aware of when she calmly told me that as a working mom in the rough-and-tumble political arena, I would have to make tough choices. We all do. In making decisions about my career, I’ve put my family first, and I’ve never regretted it, although it has meant periodically putting particular pursuits on the back burner.
When I discovered early in my pregnancy that my baby would be born with an extra chromosome, the diagnosis of Down syndrome frightened me so much that I dared not discuss my pregnancy for many months. All I could seem to muster was a calling out to God to prepare my heart for what was ahead. My prayers were answered beyond my shallow understanding of what true joy could be. Yes, raising a child with special needs is a unique challenge, and there’s still fear about my son Trig’s future because of health and social challenges; and certainly some days are much more difficult than if I had a “normal” child.
Many everyday activities like doctor’s appointments and social gatherings and travel accommodations and even mealtimes and a solid night of sleep are that much more difficult, but at the end of the day I wouldn’t trade the relative difficulties for any convenience or absence of fear. God knew what he was doing when he blessed us with Trig. We went from fear of the unknown to proudly displaying a bumper sticker sent to us that reads: “My kid has more chromosomes than your kid!” He may not be the next Wayne Gretzky, but our hearts are filled with so much pride watching Trig giggle with his sisters’ puppies, or sway to the rhythm of his Little Angels DVDs, it’s as if he were hoisting the Stanley Cup.
Granted, I know I may be more fortunate than others to have loving friends and a big, supportive family I call on to help, including a husband who spends many sleepless nights with this restless little one. (And Todd actually makes Trig’s puréed baby food!) Others aren’t so fortunate, and in our thankfulness I am made more compassionate toward others who have less.
I often think now, what would we do without Trig? He’s our “everything that really matters.”
Trig is almost 4 years old now, and every morning when he wakes up, he pulls himself up, rubs the sleep out of his eyes, looks around, and then starts applauding! He welcomes each day with thunderous applause and laughter. He looks around at creation and claps as if to say, “OK, world, what do you have for me today?”
My family knows that Trig will face struggles that few of us will ever have to endure, including people who can be so cruel to those not deemed “perfect” by society. The cruelty is more than made up for, though, when someone simply smiles at our son. Nothing makes me prouder. As I explained in a Thanksgiving article, I notice it happens often in airports. Travelers passing by will do a double-take when they see him, perhaps curious about the curious look on his face; or perhaps my son momentarily exercises an uncontrollable motion that takes the passerby by surprise. Perhaps, as an innocent and candid child announced when she first met Trig, they think, “He’s awkward.” But when that traveler pauses to look again and smiles, and maybe tells me what a handsome boy I have, I swell with pride. I am so thankful for their good hearts. They represent the best in our country, and their kindness shows the real hope we need today.
My family understands that up ahead, some days will be better than others. We will adapt and juggle things and work through it. But Trig applauds the day. And that’s what he teaches us. That’s our priority, and we’re blessed by it.
I smell bullshit on this one.
Todd still purees Trig's food? Trig should be able to eat solid foods by now. Even if he does have Down's. If he cannot eat solid food by now then Sarah and Todd have done a poor job in getting him developed.
Why has Sarah donated so little money to charities that specialize in Down's Syndrome?
I doubt Sarah and Todd take Trig anywhere, especially to airports. There has not been a public sighting of Trig in ages.
Trig looks way too much like Levi in this picture. Don't you think?
It's rich that Sarah blasts Newsweek for giving Andrew Sullivan any print but she will run to them so she can get sympathy. Guess she is really worried about Babygate being exposed and Game Change airing in a month.
Trig Palin has my sympathy
Not because he has Down Syndrome but because Sarah Palin is his legal mother.
From The Brody File
A Personal Thanksgiving Reflection by Sarah Palin:
On Thanksgiving, my family's traditions will reflect the loyal, active, robust, big family life that shaped me. We're so fortunate to be together to share the making of another year's memory. In these late autumn days with temperatures dipping to 20-degrees below zero, we'll brave Alaska's biting cold to run and skate and ride - just because we can, and for that I am so thankful. Life in America's Last Frontier is not an easy living, but it's a good living. Here in Alaska, where I'm never without inspiration, an optimistic pioneering spirit still permeates, and harsh conditions force us out of self-centeredness and towards community - often in order to survive.
This need for selflessness - and the blessings that come with it - sharpened for me almost four years ago when I was given the gift of broader horizons, clarified priorities, and more commitment to justice and compassion for my fellow man who faces challenges and fears. I was granted this through a gift that arrived in a tiny, six-pound, awe-inspiring bundle. We named him Trig.
I know America's potential for goodness, thus greatness, because I see it every day through my son. Nothing makes me happier or prouder than to see America's good heart when someone smiles at my Trig. I notice it happens often in airports. Often a traveler passing by does a double-take when they see him, perhaps curious about the curious look on his face; perhaps my son momentarily exercises an uncontrollable motion that takes the passerby by surprise. Perhaps, as an innocent and candid child announced when she first met Trig, they think "he's awkward." But when that traveler pauses to look again and smile, and maybe tells me what a handsome boy I have, I swell with American pride. I am so thankful for their good heart. They represent the best in our country and their kindness shows the real hope we need today.
I am thankful that, as in so many areas of life, the bitter people who say bitter things about someone facing challenges are so outnumbered. There have been stinging criticisms, even from people still screaming that Trig should never have been born, but we know those critics may be the loudest and most malicious, but they're not the majority.
To me, when individuals reflect the greater societal acceptance of someone facing challenges, they show the best of humanity - even by offering a simple pat on Trig's head or a knowing smile shot our way. Conversely, when a society works to eliminate the "weakest links" (as some would callously consider the disabled) or "the unproductive" (as some would callously consider the very young and the very old), it eliminates the very best of itself. When a society seeks to destroy them, it also destroys any ability or need for sincere compassion, empathy, improvement, and even goodwill. And those are the very best qualities of humanity! Those are the characteristics of a country that understands and embraces true hope! America can be compassionate and strong enough as a nation to be entrusted with those who some see as an "inconvenience," but who are really our greatest blessings. Through Trig, I see firsthand that there is man's standard of perfection, and then there is God's. Man's standard is flawed, temporary, and shallow. God's standard lasts an eternity. At the end of the day, His is what matters.
So, this Thanksgiving my family will bundle Trig up and grin while we watch him through ice-frosted eyelashes as he curiously takes in all that is around him in the crisp open air. I hope your Thanksgiving gives you the opportunity to find that reminder of what really matters, too. For me, my perfect picture of thankfulness is my perfectly awesome son. With him, all is well with my soul and I know I am blessed.
Once again Sarah uses her favorite prop to get sympathy. I think it's child abuse. And for the record no has ever said Trig should have been aborted. We all love Trig Palin, we just can't stand his legal family (Sarah, Todd, Bristol, Willow, Chuck, Sally). Note I said legal, not biological.
From The Brody File
A Personal Thanksgiving Reflection by Sarah Palin:
On Thanksgiving, my family's traditions will reflect the loyal, active, robust, big family life that shaped me. We're so fortunate to be together to share the making of another year's memory. In these late autumn days with temperatures dipping to 20-degrees below zero, we'll brave Alaska's biting cold to run and skate and ride - just because we can, and for that I am so thankful. Life in America's Last Frontier is not an easy living, but it's a good living. Here in Alaska, where I'm never without inspiration, an optimistic pioneering spirit still permeates, and harsh conditions force us out of self-centeredness and towards community - often in order to survive.
This need for selflessness - and the blessings that come with it - sharpened for me almost four years ago when I was given the gift of broader horizons, clarified priorities, and more commitment to justice and compassion for my fellow man who faces challenges and fears. I was granted this through a gift that arrived in a tiny, six-pound, awe-inspiring bundle. We named him Trig.
I know America's potential for goodness, thus greatness, because I see it every day through my son. Nothing makes me happier or prouder than to see America's good heart when someone smiles at my Trig. I notice it happens often in airports. Often a traveler passing by does a double-take when they see him, perhaps curious about the curious look on his face; perhaps my son momentarily exercises an uncontrollable motion that takes the passerby by surprise. Perhaps, as an innocent and candid child announced when she first met Trig, they think "he's awkward." But when that traveler pauses to look again and smile, and maybe tells me what a handsome boy I have, I swell with American pride. I am so thankful for their good heart. They represent the best in our country and their kindness shows the real hope we need today.
I am thankful that, as in so many areas of life, the bitter people who say bitter things about someone facing challenges are so outnumbered. There have been stinging criticisms, even from people still screaming that Trig should never have been born, but we know those critics may be the loudest and most malicious, but they're not the majority.
To me, when individuals reflect the greater societal acceptance of someone facing challenges, they show the best of humanity - even by offering a simple pat on Trig's head or a knowing smile shot our way. Conversely, when a society works to eliminate the "weakest links" (as some would callously consider the disabled) or "the unproductive" (as some would callously consider the very young and the very old), it eliminates the very best of itself. When a society seeks to destroy them, it also destroys any ability or need for sincere compassion, empathy, improvement, and even goodwill. And those are the very best qualities of humanity! Those are the characteristics of a country that understands and embraces true hope! America can be compassionate and strong enough as a nation to be entrusted with those who some see as an "inconvenience," but who are really our greatest blessings. Through Trig, I see firsthand that there is man's standard of perfection, and then there is God's. Man's standard is flawed, temporary, and shallow. God's standard lasts an eternity. At the end of the day, His is what matters.
So, this Thanksgiving my family will bundle Trig up and grin while we watch him through ice-frosted eyelashes as he curiously takes in all that is around him in the crisp open air. I hope your Thanksgiving gives you the opportunity to find that reminder of what really matters, too. For me, my perfect picture of thankfulness is my perfectly awesome son. With him, all is well with my soul and I know I am blessed.
Once again Sarah uses her favorite prop to get sympathy. I think it's child abuse. And for the record no has ever said Trig should have been aborted. We all love Trig Palin, we just can't stand his legal family (Sarah, Todd, Bristol, Willow, Chuck, Sally). Note I said legal, not biological.
Trig Palin is not retarded
But Sarah and Bristol are.
We all know Trig has Down Syndrome which will affect his ability to learn skills. No shame in that, but that does not make him retarded in my opinion. A retard is someone who does not have a learning disability and has at least an average IQ but makes repeated mistakes and never learns from them.
Sarah does not know when to keep her mouth shut, for example after the Tucson shooting. Roger Ailes told her to lie low for a while, but she produced that infamous blood libel video.
She got Paul Revere mixed up saying he warned the British, and when confronted with that fact, she still insisted she was right.
Her political ideology is wrong. Conservatism does not work and never will.
Bristol is also retarded. She actually thinks she can get away with grifting and disparaging her baby daddy. She also thinks its OK to lie and no one will call her out on it.
March 21 through March 27 is World Down Syndrome Week
March 21 through March 27 is World Down Syndrome Week. As of March 22 Sarah has yet to tweet about it or post anything about Facebook. If she really cared about Down Syndrome she would do so. Very shameful of her not to do so since she brags about being the "mother" of a special needs child. You can read about World Down Syndrome here. I will update this if she does.
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