Alyssa's First Buddy Walk

Hello everyone,

It has been a while that I blog anything (shame on me!), but I have been so busy, went back to school, work full time, kids are both at school, wife, blah, blah, blah. I will post a separate blog about Alyssa's up to date later, but today I will be talking about our first buddy walk.

First let me tell you how I started. I have been wanted for the last two years to attend, but either Alyssa was still at little peanut the first year (2010) when the buddy walk took place, or she was sick (2011) and we could not make it. This year, I decided not to miss it. I asked my boss at work if I could do a bake sell at work to raise some $ in honor for our team. She said "Yes", so Alyssa's Blessing Team had a head start. I do not know many people nor I do lots of money, so I had to bake at least twice a week in October to raise some money for Broward Gold Coast Down Syndrome Organization.This organization allows our kids to have activities and help with scholarships as well.

 I want to officially thank everyone who help us raise our goal. Everyone who donated it from their bottom of their hearts and who every bought and ate my breads and cookies.  Officially I want to say thanks to our my girls from CTU Miami, Ms. D.F. (my Director at work), Marva Gordon, and my best buddy Ada Clavijo.
I cant wait to post pictures....Hope to see you there!

Thanks again!

Comments

Post a Comment

Popular posts from this blog

Six months of love

Image
It is amazing how time goes fast, like a blink, I still remember how hard it was to know about the diagnosis and how long it has taken to accept it. Now Alyssa is six months, she is learning how to seat, she turns at her own wish and her arms are strong enough to pick up her bottle. I do not believe Down Syndrome owns her, but I do understand it is part of her. I am so proud of her.
Read more

Day 6: One thing I love about Down Syndrome

Image
Oh Boy...I have to true to this blog to anyone who reads it...there is no one thing...there are several. Down Syndrome has typical characteristic appearance, and I will point it out with my favorite model, my Alyssa: 1. Flattened nose. It is so small a kiss can cover it all. 2. Small mouth. It is so little, but give the best slobbery kisses ever. 3. Protruding tongue. It is so cute and I know it is out when she is happy or when she is really tired. 4. Upward slanting eyes. The corner of her eyes is called Epicanthal fold. They are so beautiful and clearly expressive. 5. Wider Gap on Sandal toe. It is another characteristic of Down Syndrome.Besides of being so cute to smell and make her laugh, it is great for Sandals and to grasp toys as well. I said it many times, Down Syndrome does not define my daughter, but her characteristics make me embrace her and love her even more.
Read more

A real surprise...and a note of thanks

Image
After being almost 6 months away from work (I was out on bed rest as of August due to my faulty placenta), I went back to work. I wont lie: I did not want to. I was sad to leave my family behind. I know anybody in my place would have felt the same. I started enjoying my stay-at-home situation, and my kids loved it as well, but reality must settle in and with a broken heart, I started again as of last week.  Alyssa at 2 months  It has been a rough transition; however, today I felt like I was home.  I felt the love while my friends from work gave me a surprise baby shower.  I felt special, it felt like family, it felt like home, so THANKS everyone. I had a rough year while I was expecting, and I did not have a baby shower due to my bed rest, so it really warms my heart and appreciate it.  I have been blessed to have great friends who have been there for us at our thoughest times.  Everyone has been so understanding. ...
Read more