Hector and I celebrated our 10 year wedding anniversary this May. Diego is 9 years old and just started 4th grade. Mateo is 7 years old and just started 2nd grade. Joaquin is now 4 years old and in 5 days a week of preschool and Sofia is 3 years old and in 4 days a week of preschool. We also have two amazing Australian Labradoodle babies Rocco 10 months old and Lulu 8 months old!
Living life one day at a time as a family of six...3 busy and bouncy boys and 1 Ukrainian princess. Our third son Joaquin was our unexpected blessing who came to us with a little something extra called Down syndrome and inspired us to adopt Sofia an orphan we fell in love with through Reece's Rainbow. We hope that our story will help open people's eyes to the beauty and gift that ALL children are. We are all more alike than different!
Monday, August 27, 2012
A Family Snapshot in Time
It's been WAY too long since I've posted on our family blog. Life as a family of six is so very busy! Here is a photo of our family taken at Diego's First Holy Communion this year and I also promise to be more active now that all four kids are in school!
Hector and I celebrated our 10 year wedding anniversary this May. Diego is 9 years old and just started 4th grade. Mateo is 7 years old and just started 2nd grade. Joaquin is now 4 years old and in 5 days a week of preschool and Sofia is 3 years old and in 4 days a week of preschool. We also have two amazing Australian Labradoodle babies Rocco 10 months old and Lulu 8 months old!
Hector and I celebrated our 10 year wedding anniversary this May. Diego is 9 years old and just started 4th grade. Mateo is 7 years old and just started 2nd grade. Joaquin is now 4 years old and in 5 days a week of preschool and Sofia is 3 years old and in 4 days a week of preschool. We also have two amazing Australian Labradoodle babies Rocco 10 months old and Lulu 8 months old!
A Touching Note
I received one of the most beautiful notes today that I think I have ever received. I just have to share, it's too beautiful to keep to myself.
Hi Jennifer!
Hi Jennifer!
I just got finished looking and reading all your beautiful pictures and stories...I am in tears. What a blessing you are and have been given to your beautiful family. I have to say that there is a transfixing beauty in your most precious little Sofia that melts my heart. The Angel in the sky is Our Lord coming to you and yet you are the angel.
Allow me to pass on to you something, something that is not mine to hoard. After bringing our little Raquel home from the hospital (she was in the NICU Unit for 17 days after being born) I was so grateful for her yet I wondered why? Why did God give her to us? To me? I had expressed this (amongst other things) to our priest and soon after was given a vision. There is no doubt that this was the result of not only my prayer but His beloved priests as well. In this vision (not a dream) God and I were walking together hand in hand and I was on His right. I was looking at Him and suddenly His Heart turned into hundreds of beautiful butterflies that swirled around Him. Some sparkled, some were glowing and even iridescent but all were so beautiful! Then God filled me with the knowledge that all Down Syndrome souls are from His Heart. He told me that because I had given Him my heart (I had given Him through an incredible sacrifice, my life, just before we conceived her) that He wanted to give me a piece of His. At that moment He extended His index finger towards me and one of the most beautiful sparkly butterflies landed on it. He then gave her to me and smiled. I came out of the vision at that moment and was filled with the most peaceful, calm feeling and it has never left me (about her). This story is yours too....God has given you two pieces of his heart.
Even more blessings to you and your family,
Kim
Tuesday, February 28, 2012
Our Littlest Schoolgirl
Guess who had her first day of preschool today? Oh my goodness, was it ever sweet! She was THRILLED to go to school today. Complete excitement, joy and happiness. Not one ounce of fear!
Her teacher said it was as if she had been going to school for years and that she was the hit of the class today singing and dancing. She did fabulous and I cannot wait to see her BLOOM!
Her teacher said it was as if she had been going to school for years and that she was the hit of the class today singing and dancing. She did fabulous and I cannot wait to see her BLOOM!
I can never catch this girl smiling on the camera these days!!!! But rest assured, she was BEAMING! We are so proud of you little Soft Spot!
Friday, February 24, 2012
365:Oops!
Well, I failed at my one and only new year's resolution! But this might explain things...we've been kinda BUSY!!!
First there was a little boy who turned SEVEN!
Then there was a little boy who turned FOUR! (and was SUPER sick on his birthday...SO sad!)
And then there was a little girl who turned THREE!
Needless to say, HAPPY BIRTHDAY is our favorite song these days!
First there was a little boy who turned SEVEN!
Then there was a little boy who turned FOUR! (and was SUPER sick on his birthday...SO sad!)
And then there was a little girl who turned THREE!
Needless to say, HAPPY BIRTHDAY is our favorite song these days!
Sunday, January 8, 2012
Saturday, January 7, 2012
Friday, January 6, 2012
Thursday, January 5, 2012
Wednesday, January 4, 2012
Tuesday, January 3, 2012
Monday, January 2, 2012
Sunday, January 1, 2012
365:1 A Challenge for 2012
2011 was a wonderful year but OH SO BUSY. So many wonderful things happened this past year and I had very little time to reflect and share on this blog. I've decided to challenge myself this new year and try and document each day with one photo per day for the ENTIRE year. So, to start it off right, I should post our most recent family photo. Cheers to 2012! HAPPY NEW YEAR and may everyone be blessed this year with health, happiness and good fortune! xo
The Sanchez Six at Bishop's Farm
Thursday, September 29, 2011
A Day at Bishop's Pumpkin Farm
It might be time to update our blog header with a new family photo! Check out a few of the lovely photos from Memories by Michelle. Thank you Michelle McDaid for capturing the spirit of our family...we certainly are a "wacky" group and we had a lot of fun with you on that lovely 95 degree "fall" day!!!
Check out our photos here!
Check out our photos here!
Wednesday, August 24, 2011
Just a Small Rant...
...About Prenatal Testing and Eliminating Imperfection
Not everything can be detected in an AFP, a CVS, an ultrasound or an amniocentesis. As far as I know, those tests will not determine if your child will have mental illness, heart disease, obesity, cancer, diabetes, Parkinson's, Alzheimer's, autism and the list goes on. Or do we have tests for these things in the works? Shudder...Those tests can't tell you if your child will be happy or a contributing member to society. They can't tell you if your child will grow up to be a criminal, a serial killer, a child molester or a rapist. They can't tell you if your child will grow up to be bully or a thief. They can't tell you if your child will have motivation or drive or end up being homeless. These tests won't tell you if your child will stand out, or be homosexual, or have a learning disability or be an outcast because he or she is too tall, too short, too skinny, too fat, too pretty, too ugly, too blond, too dark or too anything. I certainly know that the prenatal tests will never tell you if your child will be in a car accident or a near drowning or take a bad fall or have a birth trauma. There is NO SUCH THING as a perfect child and having those tests to rule out the forbidden DOWN SYNDROME or any other detectable birth "defect" doesn't guarantee that you will have that unattainable picture perfect human being. I'm sensitive now, more than ever, to this obsession over early detection for the purposes of eliminating "imperfect" unborn children. There is a push to eliminate children like Joaquin and Sofia. I wish people would understand that "disability" is actually very natural and it's everywhere. People come in all shapes and forms and abilities. I find it impossible to find anyone in the world that doesn't suffer from some sort of challenge or "disability". Wear glasses? Ever had braces? On a diet? Have a bad back? Ever need surgery? Need coffee in the morning? Ever had a headache? Ever need help with anything? Would you say you are perfect? Would you say you are totally healthy? My bet is each and everyone of us has some challenge or special need that they deal with regularly.
I guess this is my way of saying (and this is ONLY MY OPINION) that I don't think anyone should enter parenthood unless they understand that you take on ALL SORTS of risks, trials and tribulations, heartaches, and disappointments when it comes to having a child and you are signing up for the JOURNEY. Wherever it may take you. It's a huge responsibility. And it's a privilege. So if you aren't up for the challenge, don't have a child. To the medical industry: Let's get off this slippery slope of prenatal testing. Let's be mindful of the direction we are headed. Let's not pretend the testing is to have more "information" or to "prepare". If that were the case, I wouldn't be ranting right now. The abortion rate after a prenatal diagnosis of Down syndrome is staggering. 92% of babies who are prenatally diagnosed with Down syndrome are eliminated. That sentence alone says it all.
OK...rant is over.
On to something inspiring, amazing and beautiful. Thank goodness for that.
A link to a beautiful video:
Wonderful Works
A link to the beautiful new ministry launched today:
Wonderful Works
Not everything can be detected in an AFP, a CVS, an ultrasound or an amniocentesis. As far as I know, those tests will not determine if your child will have mental illness, heart disease, obesity, cancer, diabetes, Parkinson's, Alzheimer's, autism and the list goes on. Or do we have tests for these things in the works? Shudder...Those tests can't tell you if your child will be happy or a contributing member to society. They can't tell you if your child will grow up to be a criminal, a serial killer, a child molester or a rapist. They can't tell you if your child will grow up to be bully or a thief. They can't tell you if your child will have motivation or drive or end up being homeless. These tests won't tell you if your child will stand out, or be homosexual, or have a learning disability or be an outcast because he or she is too tall, too short, too skinny, too fat, too pretty, too ugly, too blond, too dark or too anything. I certainly know that the prenatal tests will never tell you if your child will be in a car accident or a near drowning or take a bad fall or have a birth trauma. There is NO SUCH THING as a perfect child and having those tests to rule out the forbidden DOWN SYNDROME or any other detectable birth "defect" doesn't guarantee that you will have that unattainable picture perfect human being. I'm sensitive now, more than ever, to this obsession over early detection for the purposes of eliminating "imperfect" unborn children. There is a push to eliminate children like Joaquin and Sofia. I wish people would understand that "disability" is actually very natural and it's everywhere. People come in all shapes and forms and abilities. I find it impossible to find anyone in the world that doesn't suffer from some sort of challenge or "disability". Wear glasses? Ever had braces? On a diet? Have a bad back? Ever need surgery? Need coffee in the morning? Ever had a headache? Ever need help with anything? Would you say you are perfect? Would you say you are totally healthy? My bet is each and everyone of us has some challenge or special need that they deal with regularly.
I guess this is my way of saying (and this is ONLY MY OPINION) that I don't think anyone should enter parenthood unless they understand that you take on ALL SORTS of risks, trials and tribulations, heartaches, and disappointments when it comes to having a child and you are signing up for the JOURNEY. Wherever it may take you. It's a huge responsibility. And it's a privilege. So if you aren't up for the challenge, don't have a child. To the medical industry: Let's get off this slippery slope of prenatal testing. Let's be mindful of the direction we are headed. Let's not pretend the testing is to have more "information" or to "prepare". If that were the case, I wouldn't be ranting right now. The abortion rate after a prenatal diagnosis of Down syndrome is staggering. 92% of babies who are prenatally diagnosed with Down syndrome are eliminated. That sentence alone says it all.
OK...rant is over.
On to something inspiring, amazing and beautiful. Thank goodness for that.
A link to a beautiful video:
Wonderful Works
A link to the beautiful new ministry launched today:
Wonderful Works
Wednesday, August 17, 2011
First Day of School Jitters...for the Mama!
Joaquin has his first official day of full inclusion preschool tomorrow morning at 8:30am and I'm a nervous wreck. We have been looking forward to this day since he turned 3 in February. This is what we have always wanted for him...to have the same preschool experience that any typical child would have. The same that his brothers had at this age. Joaquin is social, easy going, very flexible, enjoys learning and loves people so why am I nervous?
Well, I wasn't nervous until I went to the "meet the teacher" day on Tuesday. I was greeted warmly by the teachers and everyone was very excited to see Joaquin. The teachers (all 3 of them) said they have been looking forward to Joaquin attending the preschool. I picked up the preschool newsletter and the calendar of activities planned and made sure that Joaquin would be on the roster and we happily went home. I eagerly sat down to read through all the paperwork, so thrilled for Joaquin, and then it hit me. I read that one of the first activities next week is to bring in a photograph of your family to share with the class. Oh my gosh. How is Joaquin going to share with the class? He can't talk. It hit me. I mean sure, he can identify each of us in the photograph with prompting and I'm sure he will smile and point at his family members but that's about it. Typical three year olds talk. Some talk A LOT. But I'm certain every child in that room will be able to talk about their family. Joaquin won't. I get teary eyed just thinking about it.
I know I'm doing the right thing. I know Joaquin will learn best from his typical peers and he will learn best to TALK from his typical talkative peers. But it's still hard and it hits you.
Deep breaths as we cross this bridge into new territory. Typical peers. Peers where the difference in abilities will be VERY evident. Painful at times. But it's the best for Joaquin because this is REAL life. Not the safety bubble that special ed provides. Special Ed has a place and a time but I see now how easy it would be to crawl back to the safety net of it. BRAVE. Must be brave. Joaquin deserves this opportunity and I'm certain he will handle it WAY better than I will. Deep breaths.
Well, I wasn't nervous until I went to the "meet the teacher" day on Tuesday. I was greeted warmly by the teachers and everyone was very excited to see Joaquin. The teachers (all 3 of them) said they have been looking forward to Joaquin attending the preschool. I picked up the preschool newsletter and the calendar of activities planned and made sure that Joaquin would be on the roster and we happily went home. I eagerly sat down to read through all the paperwork, so thrilled for Joaquin, and then it hit me. I read that one of the first activities next week is to bring in a photograph of your family to share with the class. Oh my gosh. How is Joaquin going to share with the class? He can't talk. It hit me. I mean sure, he can identify each of us in the photograph with prompting and I'm sure he will smile and point at his family members but that's about it. Typical three year olds talk. Some talk A LOT. But I'm certain every child in that room will be able to talk about their family. Joaquin won't. I get teary eyed just thinking about it.
I know I'm doing the right thing. I know Joaquin will learn best from his typical peers and he will learn best to TALK from his typical talkative peers. But it's still hard and it hits you.
Deep breaths as we cross this bridge into new territory. Typical peers. Peers where the difference in abilities will be VERY evident. Painful at times. But it's the best for Joaquin because this is REAL life. Not the safety bubble that special ed provides. Special Ed has a place and a time but I see now how easy it would be to crawl back to the safety net of it. BRAVE. Must be brave. Joaquin deserves this opportunity and I'm certain he will handle it WAY better than I will. Deep breaths.
Things That Make You Go "Hmmmmm"
We're not sure who is to blame here but we got a new piece of furniture and not 10 minutes after the delivery guys left I turned around and saw this...
Yes, that is Sofia inside a glass cabinet. She was all giggles and smiles and Joaquin was one foot away from it...hmmmmmm...
Yes, that is Sofia inside a glass cabinet. She was all giggles and smiles and Joaquin was one foot away from it...hmmmmmm...
Tuesday, July 26, 2011
The Healing Smile
A post from Hector:
This morning when I woke up I went to check my email and there was a message from a comment posted on Sofia's old blog. It brought tears to my eyes, it read:
Every day when I wake up in the morning or I get back from work at night, Joaquin's smile melts my heart as well. He has that effect on people, he demands hugs from mostly everyone known or unknown. I still hold my breath for a second or two when it happens with strangers, and every time his smile wins, and he will not let anyone off the hook that easy. Moms will want to hold him until he's had enough, dads will do it for a minute or two and then as they try to put him down he will hold on for a little bit more. He needs to rub his hands on their cheeks and feel the prickly beard on the back of his little hands. And most of the time they give in to his request to be held and enjoy this little baby bear cub embrace. And I have to tell you, it is the most wonderful embrace you've ever known.
Some of you know about the GQ fiasco that happened recently. I did my part and sent a letter to the editor expressing my opinion and telling him I won't be patronizing his magazine anymore unless they made things right. I've been a subscriber for many years and I asked them to issue a public apology and write an article or have special coverage on Down syndrome. How about Joaquin on the cover? I understand that as part of the Down syndrome community I am constantly on edge about insensitive remarks and the use of the "R" word, but my outrage about what was printed goes beyond sensitivity. It was probably the worst insult I've ever heard. It would take me a thousand pages to describe how wrong it was, but I'm over it. It is obvious that the guy who wrote it has never known someone with Down syndrome. Or perhaps he is plain and simple an insensitive asshole.
Joaquin and Sofia's story along with all the beautiful children of The Sisterhood and the many more we are blessed to know are changing lives one smile at a time.
And now some eye candy...



hello, my name is Michelle and I saw you (Jen) today at the twelve bridges park. I was having a hard day thinking of my miscarriage and how I would be having the baby any day if nothing had happened. Your little joaquin looked at me and gave me a beautiful smile that just melted my heart. I heard you call out Sofia's name and something rang a bell. I thought maybe I had read an article about you guys on kidaround. I went home and looked you up! How amazing that little Sofia is now with you guys! You guys were a ray of sunshine in my sad day. I know God sent you guys to that park today, and He showed his love to me through your angels!
Some of you know about the GQ fiasco that happened recently. I did my part and sent a letter to the editor expressing my opinion and telling him I won't be patronizing his magazine anymore unless they made things right. I've been a subscriber for many years and I asked them to issue a public apology and write an article or have special coverage on Down syndrome. How about Joaquin on the cover? I understand that as part of the Down syndrome community I am constantly on edge about insensitive remarks and the use of the "R" word, but my outrage about what was printed goes beyond sensitivity. It was probably the worst insult I've ever heard. It would take me a thousand pages to describe how wrong it was, but I'm over it. It is obvious that the guy who wrote it has never known someone with Down syndrome. Or perhaps he is plain and simple an insensitive asshole.
Joaquin and Sofia's story along with all the beautiful children of The Sisterhood and the many more we are blessed to know are changing lives one smile at a time.
And now some eye candy...
Tuesday, July 12, 2011
I Hope You Dance
Here is Sofia with my dad, her Grandpa, at my brother's wedding this weekend. All our kids ADORE music and dancing so we love a good wedding!
Weddings always remind me of what is most important in this life. To love and embrace life...to dance. Life is so busy right now and hectic and stressful. Raising four kids (all under the age of 8) is a lot of work but I'm not complaining. We feel so blessed. We have four healthy and happy kids and we will never take that for granted.
Weddings always remind me of what is most important in this life. To love and embrace life...to dance. Life is so busy right now and hectic and stressful. Raising four kids (all under the age of 8) is a lot of work but I'm not complaining. We feel so blessed. We have four healthy and happy kids and we will never take that for granted.
Sunday, July 3, 2011
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