Journaling about my kids (plural- wow!) for me; updates on our life for our wide circle of loved ones is for, well, our loved ones; sharing about life with a spunky toddler and the emotional highs and lows of having a wonderful baby with Down Syndrome is for anyone who might be on a similar journey.
Also see my blog: www.lupesmom.blogspot.com

Saturday, July 4, 2015

Liam turns 4 in Big Sur

July 2015
We went to Big Sur for Liam's birthday but this time we camped out for the first time as a family.  Yeah!  P has never camped before (well, except for that time in the Lacandon jungle of Chiapas, but I'm going to say this was the first time because we didn't have indigenous guides planning everything.   Well, we did have the tips thought!)   My brother and sister-in-law went with us and they have camped all over the world, literally!
Lupe camped once in our backyard in Atascadero with her tios.
I grew up camping in Big Sur, before it was mobbed by hoards of people from all over the world.
I think Liam's favorite part was the marshmallows
I love the portobello mushroom burgers that my brother and sister-in-law made wrapped in foil over the campfire
Bacon in the morning (veggie bacon.  What's that you ask?)
I
McGraths in caps.  
M
Liam loved throwing rocks in the river.  
And speaking of rivers, we love to end our trips at the River Inn 










Wednesday, June 17, 2015

Yesterday we were watching whales


Yesterday we went to Avila beach to see the whales. From the pier we could see 4 to 6 humpback whales breaching just yards away.  It was spectacular.  
But Liam fell asleep in papa's  arms.    And today we are in the hospital again.  We don't know exactly what's going on but Liam is fighting some kind of infection.  He has a fever but his oxygen levels are good.  What is concerning is that half of his face is red and swollen up and he can barely look out of one eye. (Black marker is to keep track to see if the redness spreads) 

Update.  It's the next morning now.    10:00 and we haven't seen the dr yet but though his eye is still swollen and face puffy, the redness is less pronounced.  No fever 
He ate a ton of breakfast 
He looks like he got in a fight or a bug bite.   But we still don't know what the cause is.  One of the night nurses was the mom of a girl in Liam's canceled swim class and we saw a family we know with a baby here in the Pediatric Unit.   Small world. 
I'm so grateful pedro and I each got a day off work.  We could have taken turns but it's so much easier and reassuring with both of us here.   And we have family and friends to help.   Thank you God.  

 Third night here.  Slowly improving everyday.    He's eating well and a good lil' trooper.  
He's as independent as ever.   We have got the hang of going to the bathroom and having to roll down with the IV machine.  He

Tuesday, May 19, 2015

Inclusion


"They" think that my son needs to be in a special day class in order to learn.  Apparently the "IEP team" determined that this was best even though Pedro and I are part of that team and our opinion was not asked for
Our wish is that Liam go to his neighborhood school which is three blocks away and his sister attends.  Our school is our community.  We have been a part of it for three years now. 
Here we are heading to Math Night. We live three blocks away
Liam liked it so much he didn't want to leave. 
6/12/15 update 
Sounds like our voices have been heard
Here is what I prepared and read in the meeting:
We feel we should elaborate with more detail our hopes and dreams for Liam.  SLO is a small community and we love spontaneously  bumping into friends at Farmer’s Market, knowing our mail carrier and saying hi to people as we walk to school.  This is what it means to be part of a community.  We see Liam living independently, working and contributing to his community.  We see him walking downtown and seeing people he knows and engaging in conversation.
Being part of the community can’t start too early, and in fact, Liam is already part of many communities.  Liam has been going to our neighborhood school since he was a baby.  When his sister was in preschool, he would sometimes sit on the floor next to her during  the initial circle time.  Other kids would put their arms around him.  During sister’s kinder and first grade years we walk in to pick her up at the end of the day and half the kids turn around and shout “Liam!”  He hugs every teacher his sister has introduced him to.  When I gave an art lesson in her class, he followed me around also pointing to the kids art work and making his own “comments”.  When one of his first grade buddies said “Hola” to him, gave a hug and walked away, Liam called after “Como estas?” Spontaneous speech in two languages!  The first grade class made get well banners when he was in the hospital.  Inclusion starts from the beginning.

We see the school as being supportive of the strong education Liam receives at home.  Home is an environment ripe with learning and rich in language and has been since day one.  Especially since we have essentially homeschooled Liam.  He has had no therapies or services for almost a year, and he has gone from 30 words to maybe 200 or more, in two languages- with couplets abounding and spontaneous phrases emerging.  We aren’t asking the schools to be the primary teachers of our son, but to be one piece of a community of educational support which includes us as parents. We are looking to give Liam a preschool experience in the community that already embraces him.  It takes a village!

As the evaluations saw Liam as being so far behind developmentally, it was a wake up call to us as parents to rededicate to his home program which we had been slack on for many months.  A renewed dedication to exercise and self care is one of our many steps to being even more dedicated and enthusiastic parents.  There’s some straight up honesty for you!  In the last 2 weeks Liam has learned all his colors, much of the alphabet and is working hard at sequential processing activities.  

Liam loves Pacheco.  He loves the teachers and many of the students.  He loves walking to school and being part of the group.  He deserves the opportunity to go to his community school and give it his best shot.  Can’t we find a way to give him this opportunity?   

Also:
 Goals for Liam:

Liam will flourish in an environment that supports his understanding and expression in two languages.  Liam will benefit from teachers who understand his language/cultural background.
To be ready for a 90/10 Language model at Pacheco, Liam needs more exposure to Spanish in a classroom setting.


Liam will maximize his full potential by learning and playing with typically developing peers, fully included in a general education preschool with support.  


Because of his delays, Liam will benefit from an instructional aide part time to support him in a fully inclusive classroom.  Behavior is not an issue, but toileting, fine motor and perhaps transitioning need support and attention.  

Liam needs help to continue to improve articulation and expand his utterances to 3-4 word sentences.  He could benefit from techniques using straws, whistles and horns to improve facial muscle tone.  Liam learns well with 1:1 speech therapy.


Processing is the key to much of Liam’s development.   With individual support and focus on increasing Liam’s visual and auditory processing, his potential will grow by leaps and bounds.

Also:
I understand we have a lot to talk about today.  I’d like to get down to the nitty gritty if we may.
Liam will be attending Pacheco preschool in the Fall. He could benefit from- and he is entitled to- some support and that is why we are here today.  We would like to continue working on his goals and making modifications.  
1.We would like to take him for speech therapy 2-3 times a week.  If there is a law or policy that prohibits him from receiving those services at his school we will take him to PEEP.  We have transportation covered, even though he qualifies for it on his IEP.  2.We think the right Aide could be very beneficial to him in the classroom.  Special Education law states clearly that he has the right to try inclusion with support.

I understand that you are offering what is typically available for a child in this area with a similar diagnosis.  However, you are failing to offer a full range of options, including full integration in his community school with typically developing peers, which is the only placement that meets the definition of LRE as intended by State and Federal laws, best practices and his right to be educated in the same school that he would attend if he were not disabled.  

We are not ignorant of his delays, but  we will not consider a SDC until he has been given the chance to attend his community school and we can evaluate his progress.  The proportion of disabled to non disabled children in a class should more accurately reflect the community, which is why the “reverse inclusion” you mention does not seem sufficient.
You must be familiar with the Holland Case in which it was decided by the court that a disabled student could be educated in a regular classroom “if the student can receive a satisfactory education there, even if it is not the best academic setting for the child”
Liam will benefit socially from a typical preschool.  He will not be disruptive to the learning of other students.  It will not cost the District more.  and he WILL meet some of his goals successfully there.  

The US Department of Education’s Draft Policy Statement of Inclusion of Children with Disabilities in Early Childhood Programs states:
(page 3) Defining Inclusion
That is from the Dept of education.  If you want me to send you all the other research that supports Inclusion I am happy to do so.
Under LRE requirements, the IDEA presumes that the first placement option considered for each child with a disability is the regular classroom the child would attend if he did not have a disability.
Diane in your emails you mentioned all the ways in which the IEP Team offered or determined things.  It felt very exclusionary.  Absolutely no one in this room knows Liam like we do.  Correct me if I am wrong, but the tone indicated that your offer was all or nothing.  

Liam’s disability is not severe.  The first page of his IEP indicates that he cannot function well in a preschool with peers.  This is not accurate.  Let me repeat that we are not denying that he has delays.  But he has A LOT of potential and many of his goals can be met in a regular classroom.  They are skills that most beginning preschoolers are trying to acquire.  

Can we work together on this?

Also:
Liam has a sense of humor which shows itself in both  English and Spanish.  

He plays for long periods of times with balls and dolls with a lot of focus.  He will play with his sister or independently beside her.  

He loves books, the library and his bedtime story routine.  He will “read” favorite books independently or bring a book and ask for it to be read.  
He shows pre-writing skills, recognizing his name, several different letters, and making marks on a page as he says out loud the letters of his name.  Liam has learned to read some high interest words.

He uses spontaneous speech in courteous ways, expressing “Thank you” for something or saying “bless you” after someone sneezes, without prompts.  He mentions the the kids from preschool and makes attempts to tell us about his day.
He kisses his sister when she cries.  
He is curious and attentive.  Loves playing ball, dancing, jumping and hanging from a bar.  At his soccer class with typical peers one mom commented he was the best in the class!
At the same time, he has some needs.  Liam needs help and practice with annunciation, and expanding his phrases to 3 and 4 words.  He has an emerging strong will and will occasionally walk away and not stop when asked.  His processing level is of utmost concern and as it improves, so will all areas of his development.  No test can measure his potential.

He has UNLIMITED POTENTIAL and he is ready to take on the world! 

And finally:
What do we want Liam to learn?

To be curious and to try new things
To be excited to go to school every day.
To play with other kids.
To communicate in a way that he is understood.
To continue to differentiate between the two languages he knows.

To understand and participate in routines.
To go potty independently
To follow directions well without too many prompts, and to increase amount of directions/steps he can understand and follow through on.
To steadily improve fine motor skills.

What do we want teachers/other professionals to know:

To have high expectations
To see him as Liam, and not as any earlier known ideas about Down syndrome.
To know that he can understand more than he can communicate
He needs time to respond when asked a question.
He is learning and processing two languages- there is a lot of activity going on in his head!  This is a good thing.
He loves to learn.
He has a bright and illimitable future ahead of him- we can all help make his dreams come through.  
It starts now.



That was a lot!

Thursday, April 2, 2015

Grocery shopping was fun today!

Most of the time we do grocery shopping as a whole family so that one of us can get the shopping done and one of us can pay attention to the kids meaning mostly Liam.  I don't often do the shopping on my own with the kids but when I do Liam  stays seated in the cart to make things easier. 
Today however....
First we went to the farmers market which is just a very tiny one on Sundays.  Liam helped carry things like the bag of kale. We went to a stand where the man said "Hola" to Liam.    Then Liam responded "Hola.   Como estas?"   Ha! So proud of my bilingual boy learning how to have conversations. 

Then we listened to the man playing guitar.  He finishes a song and Liam applauds with enthusiasm "Bravo!!" He says, then adds, "Let it go" making a request!
And shopping was a dream! Liam and lupe walked the whole time.  We kept Liam engaged talking to him and having him help choose things to put in the cart.   And we did this in two stores.  No sitting in the cart. Lupe was an awesome big sister. 

Monday, March 30, 2015

Poor little guy


Here's what I do when my poor little guy gets sick.  
We let the fever do it's job fighting off the sickness and tried to just keep him cool and comfortable.  Treating his cough is harder. 
He slept and slept and slept all night and most of the morning and when he woke up he was dehydrated and hungry.   I made him some hot brown rice with Chia seeds,apples and strawberries and hemp milk.  He's eaten three bowls and he wants to feed himself but his poor little hand is shaking from weakness.  
Then he gets some of his Nutrivene-D multivitamin in applesauce and then some vitamin D3, probiotics, echinacea and colloidal  silver.   
And of course some Breathe oil and Thieves.  
However, things took a turn for the worse. So we went to the pediatrician's office at 4:30 pm and they sent us to the ER so that they could do a chest x-ray and rule out pneumonia.  5 1/2 hours in the ER and he seemed to perk up after oxygen breathing treatment and then iv fluids. No pneumonia.  Blood work fine.  They sent us home.  After seeing police dragging people in to the ER and a woman screaming we were glad to go. 

He seemed better but the next day right before our follow-up appointment he spiked a pretty high fever again. So back to the hospital and after more studies and more breathing treatments determined that he had RSV.  The coughing continued and he was complaining about it hurting.  Antibiotics were started for a possible sinus infection.  We have stayed here two nights and he is breathing better.  Everyone has been really nice.  

Pedro and I have both taken a day off of work and Lupe has been staying with the grandparents and been picked up from school by friends. The kids miss each other.  
How GRATEFUL I am to have family here.  
Lupe's first grade class made pictures for Liam and sent him some toy cars to play with.  How amazing! Liam is loved in first grade.  
So sometimes hospitals and medicine are absolutely the best route. We have been struggling for so long with his on again off again congestionand raspy breathing.  It's been his only real health concern (And with Down syndrome there could have been a lot more problems)    We have tried diet changes and other things.   So when asthma was mentioned and the idea of flushing out his sinuses a lot more often and using an inhaler when we hear the wheeze, well, if this helps his overall respiratory health then we are grateful for some solutions.  But something is triggering this and that is what I'd like to find out.  
Parenting is damn hard work.  
He's better. 


Tuesday, March 10, 2015

Pre IEP evaluation hormonal rant

I love my family so much it hurts.  I really am grateful to be on this journey and to have become a person who has so much fucking respect for parents of children with special needs and for the truly open and caring professionals who are trying to help.  
But....
Sometimes I am just so fucking tired of it all.  I am tired of the assessments and seeing all the things that my three-year-old is not doing that others can.   I am tired of how much time it takes to learn new things.  I am tired of all the mental energy put in to researching and experimenting different things to help my child.  I am tired of the  negative thoughts I have when I hear parents complaining about the small things their typical child is or is not doing.  It is so hard to watch things that kids can learn so easily without a parents second thought when it takes so much effort on my part to teach my son to do the same thing. 
Sometimes I want to say screw all this worry I have but I can't. I can't because special needs or not I am a parent and we all do what we have to do for our children

So after the chance to do some errands by myself I took a quick hike on the way home.  Just 15 minutes.  And I went off the path and sat in the middle of a field of yellow flowers.  But I still felt gray. 
I tried to feel peaceful and look at the little ladybug hopping along the grass stems.    It helped just a little. I am feeling hormonal today and it was not the best day to watch my son being assessed and I will just have to live with that and feel what I feel. 

Monday, March 2, 2015

Little things that are BIG

Monday: Liam just said "mama help".  I have been prompting him to say "help please" for ages and he will repeat it when I have prompted him.  This was the first time he did it without any prompting from me.  What a useful thing to be able to communicate!

Tuesday: "good morning Lupe "  "mmm yummy mama". "thank you mama". unprompted

Wednesday: Liam offers me a cheerio and I say no thank you.  Then he laughs and says "Liam mouth, Boca".  My bilingual boy
Tuesday of another week:  "that one".   "Other side" 
He put a ball in my shirt and said "baby tummy".
Yesterday at the park he saw a cup on the ground and said "dirty".   This is a big one too because I don't think he has seen us picking up trash in public and throwing it away very often and he sometimes needs prompting him to throw things away.  It was a very good connection

He now brings me a book and says "read".   He had lots of favorites and says them by name.  

Liam probably has around 150 words or more that he can say.  But what I am seeing recently is him not just saying words or repeating me but actually using spoken language to communicate his needs.  THIS is important. 
Wait, and did I already mention that he says "thank you mama" spontaneously? That's just awesome for any three year old  I think. 


Thursday, February 26, 2015

What do I want?


What to do I want for my kids in life?  
Aside from wanting liam to be happy and healthy, I want him to have friends and be loved. I want him to be able to go anywhere he wants and communicate with people and be understood. 
I want to do whatever I can now even at three years of age to help him be able to live as independently as possible when he's older. 
I want him to be interested in something and be passionate about it. I want to help fulfill his dreams however outlandish and impossible they may seem at the beginning. 
And for Lupe? Well pretty much the same actually. Liam may have an extra chromosome that affects many aspects of his life but really my kids are more alike than different.  They are both the children of Sara and Pedro.  And we want both of them to reach for the stars


Friday, February 6, 2015

Girl Scouts

I have to admit I had my doubts about the Girl Scout cookie selling. And a week before the official date of cookie selling season I saw many mom friends posting on Facebook to get everyone's orders in because ...the cookies were coming!!  So I did the same thing and had friends and family from out of town wanting to reserve cookies.  But then the day after receiving the cookies we set up a stand in front of the house and Lupe started on her homework as she called out her first tentative "cookies for sale!"  
And slowly the people started to come.  In three afterschool sessions Lupe had sold out of her 36 boxes. I started to go back on my online promises as we met college students who used to be Girl Scouts and the Cuban couple from up the street who heard Pedro speaking Spanish. 
And I realized that this was what it was all about.  Who was I to take away from Lupe's learning experience?  It's not a competition.  And it doesn't matter if you sell them all or not. 
What matters is a six year old girl learning to use her voice, meeting her neighbors and practicing her math while counting her money. 

Thursday, January 29, 2015

Progressing and present

Last night after asking Lupe about her favorite part of the day I asked Liam.  He went "ahhhh...." so i thought i would ask him some specifics.  I asked if he liked seeing Bob in LA and he said, "Bob. YEAH!!" and put his arms up in enthusiasm.  Yesterday we went to LA for our most recent neurodevelopment evaluation with Bob Doman of NACD.
The best thing I heard from Bob was that Liam was "present" and this may seem a small thing, but it means everything to me.  Here's why:  when Liam was born I knew nothing about Down syndrome or special needs.  And I have to admit, my biggest fear was that he would have a vacant look in his eyes, that he wouldn't be present.  It's hard to admit fears, but in doing so sometimes you find you're not alone.  Someone else may be inspired by your honesty and voice and share their own hopes and fears.  This conversation started because i was recounting our breakfast experience that morning in a restaurant in Santa Barbara on our way to the evaluation.  Pedro ordered coffee and decided to put honey in it.  After one more refill, and added honey, Pedro got a third refill.  As soon as the waitress had poured the coffee Liam reaches over and hands Pedro the honey bear, saying "Honey!"    We were all impressed with his memory and that's when we were told that Liam was very "present" by the evaluator who has guided us over the last three years.
This guidance is reassuring to say the least.  I  am not concerned that the process to start speech therapy locally is taking months.  I am not worried that we are "losing time" in the wait.  Liam is most definitely not falling behind. I am not worried that our guides and trainers from NACD will ever underestimate Liam's potential. Au contraire.  They will make sure he is always progressing and we the family are in complete control.  No power struggles.  No personality conflicts.  No time wasted trying to set up meetings with psychologists, special ed directors, general ed teachers, speech therapists, etc.  No wishing we had more hours or a different therapist.  Just a quarterly day trip and as much contact as I want through phone calls, videos emailed, Skype.  I decide.  I realize it's not for everyone, but it is working for us.
And Liam's language is exploding!  He puts two words together all the time, sometimes more.  He copies what we say. He names objects around him.  Just now he saw a capital "A" in a book and pointed to it saying "A, apple", referencing an ABC phonics song he likes to listen to.  Earlier he told me outside, "Bubbles up high!"  His short term memory is improving. I've been trying to keep track of all the new things he's doing and just can't anymore! It's so much! 
Our goals going forward are going to be: potty training (we got some good ideas and think he is ready for the next step), still working on behavior/eloping, no choices at meal time (as Lupe's teachers say, "you get what you get and you don't throw a fit"), giving Liam more chores (like cleaning under table, matching socks, putting silverware away), language and processing.



New York New York

2015.  Oh 2015, you are going to be an awesome year.  In March I turn 40 and in July Pedro and I celebrate 10 years of married life.  Ten years!  So...... we are taking a trip, JUST US!  Oh my God, this is only possible because I have the most amazing parents in the world and they all live here, all four of them.
Lupe has gone away for a whole weekend with the grandparents before, and Liam has gone for a sleep over once.  It went well.  Well, he fell off the bed, but that is an easy fix.  I would normally be most amazed at the fact that we are going to be away from our kids for five days, for the first time ever.  But, all I can think about is New York City!  For anyone who might not know, I lived there for 6 years in my twenties.  Six amazing years.  1997-2003.  And I haven't been back since, it's been 12 years.  What?  I haven't been back to NYC in over a decade?!  It's amazing when  you are old enough to start thinking in decades. I will soon have been alive for four of them.  And Pedro has never been.
I want art and culture and diversity, multiple languages heard on the street, music and dive bars.  Pedro wants Times Square and tourist attractions.
So, here's what is keeping me up at night, my head swimming with memories, fleeting images of street corners, random hours on subway trains, cheap slices of pizza and happy hours at Brooklyn bars.


Pizza slices from Sal in the LES who's been serving New York pizza for eons.
Walking from Little Italy, where there are still old Italian guys in bars that look right out of a movie, to Chinatown wondering how to order some good authentic Chinese food.
Storefront signs with Chinese lettering and Hebrew.
Sixth street in the East Village, an entire block of Indian restaurants with excessive amounts of multicolor Christmas lights.
An Irish pub with straw on the floor.
The 9/11 memorial.
Pretzels in Times Square and swing dancing.
Seeing HighLine park for the first time.
Deli coffee where they prepare it for you and a bagel with scrambled egg.  Is it still $2.99 for that combo?
A new ferry line on the East River, stopping in Greenpoint, Williamsburg, DUMBO, the Lower East Side.
Maybe a fancy drink at the Ritz-Carlton on Central Park South.
Taking Pedro to the Met.  The lions in front of the main Public Library.
People from every corner of the globe.
My Uncle Patrick and Aunt Mariah.
My old stomping ground of Orchard Street, just off Houston, around the corner from Katz's Deli.
Seeing the Statue of Liberty for the first time.
Brownstones and African restaurants and black culture in Brooklyn.
Canal street.
Museums and art spaces in graffiti covered building in Long Island City.
Art. Art.  Maybe a little bit more art.
Souveniers for my kids.
Showing Pedro around my city. Oh my god I can't wait.

Thursday, December 11, 2014

"Go back"

Here's the latest.  Snippets of thoughts.
One day recently I told LIAM we were going to the sink to wash hands.  We went in and I started to get the stool when he pushed me and said "Go back!!!!"     Excuse me?  "Go back!" He says.   No, he insists.   Something important is happening here, he wants to do it himself!  This has been happening for a while now, but here he came out with a command, a phrase that we hadn't intentionally taught him.  He sets up the stool, climbs up and sticks his hands under the faucet. (He can't reach it to turn it on). I turn the water on and as soon as I do he tells me to go back again.   I stay, squeezed between the stool and the door while he washes.   I want to let him continue indefinitely but even with this rain, California is still in a drought!

We play with a stuffed animal unicon and he calls it a puppy.   I say "no Liam, that's not a puppy, it's a unicorn!"   And he cracks up laughing and calls it a puppy again.   This goes on for a whiLe and he laughs harder each time.  

Today I volunteered at lupes class doing an art project.  As I walked around making comments on each kids project he followed me, also touching the pages and talking about them.   Oh, and when we first walked in half the kids shouted out, "Liam!"   I love that he is so loved!

His four new words this week, written words to learn, are: oatmeal, eggs, banana, kiwi.   He knows them already and it's only been four days.  

6:30 am.   He comes to the side of the bed with the little yellow sauce pan I usually make his oatmeal in and hands it to me saying "oatmeal".

His "NOOO!" Is getting louder and stronger.

Papa was his favorite for two months, wanted nothing to do with me.   Now he's mixing it up, you know, to keep us on our toes.  So we never know what will happen.   One day he wouldn't let me push him in the shopping cart, only Lupe.   One night every time pedro looked at him at the dinner table he went "arhhhhghgh!" (or something like that) and made a horribly pissed off kind of face.  He only seems to come to the table to eat when he decides to come to the table.   Otherwise there are torrents of tears.   He hasn't suffered form hard dry boogers in ages, the Crying keeps those nasal pasajes well moistened.  

He tries to tell us things and sometimes we don't understand.   We'll repeat back to him what we hear, he'll pause, shake his head and say no, then repeat it.  Poor guy.  It must be so frustrating.  

In preschool, the kids sometimes interact with him, though not quite as much as they do with the rest who can all hold conversations.  Sometimes this is hard for me.  I really appreciate the parents who have developed, and show great affection and care for him.  They are the ones who also encourage their kids to interact with him.  The kids like him, they just think he's younger.   And he is a bit, after all he is 3.5 and it is a class for three and four year olds, one even just turned five.  

I still wish I lived closer to another family doing NACD, the neurodevelopment program we do with him. I have decided to try speech therapy locally.   If we have a good match with someone who helps us implement our program, fantastic.  If it's not worth our time we'll stop.   Part of me wants to show parents it can be done, to go without "the system". 

Liam's hair has crazy red highlights.  My scots-Mexican boy.

Lupe is doing well.   Has a hard time with math concepts.  Enjoying Girl Scouts.  She's a good sister.

Next year.  2015   I turn 40 and pedro and I celebrate ten years married.  We're going to New York.