July 2008
July 31, 2008
One morning I was flipping channels and I see these amazing little cupcakes on the Martha Stewart show. I stopped and started to watch the show...this amazing personality starts demonstrating her cupcakes and I was amazed on how beautiful they were. They mentioned her blog www.bakerella.com and I immediately logged on. I am not sure why but I decided to contact her...this stranger on television..
To my surprise Angie contacted me back. After sharing Savvy's story with her and asking her to create a pop in honor of organ donors (our donor angel) she told me that my email caught her attention because she too is a recipient of the amazing Gift of Life. She is a recipient of a kidney from a donor angel.
She has created these amazing cupcake pops...when I saw them tears flowed...I had explained to Angie that I like so many others want to celebrate this Gift on the anniversary...I understand the significance and the sacrifice behind the Gift but as a 2 year old child...Savannah is too young to understand...then I had thought about how our donor was a 2 year old child...what child does not love cupcakes? What a beautiful way to honor our donor angel.
Thank You Angie...thank you for this beautiful tribute...if you have a minute please go to www.bakerella.com and leave Angie a message...and share these beautiful creation with others...for the message behind this simple little pops is a life saving one!

Thursday, July 31, 2008 Pops for a purpose A couple of months ago, I received an email from a reader. She told me the story of her baby daughter, Savannah, and how she received a liver transplant when she was one. She explained how much she and her husband want to raise awareness for organ donation. And, when she asked me to create a cupcake pop for fundraisers to honor Savannah's 2-year-old donor, I knew what I had to do.
I called and told her I would and then I told her my story, and we both cried.
You see, today is my sweet sixteen. It's what I call my second birthday. Sixteen years ago I received a phone call asking me to come to the hospital right away. The voice on the other end said they had a possible "match." I was sick, both of my kidneys had failed and I was on dialysis. But, later on that evening I was in surgery for a kidney transplant. And, the next day I no longer needed dialysis – I was the recipient of the greatest gift that can be given.
I don't have the words to describe all the feelings I had then and still have now. But Savannah's mom reminded me how I was given a second chance and how I can do more myself.
So maybe, you'll read this and take a minute to think about organ donation. Or, the next time you renew your license, you'll remember these pops or Savannah, or me and change a life.
Here's Savannah's story (have a kleenex handy)
Above: cupcake pops with the green ribbon (a symbol for organ donation) Below: Some other combinations with the same color scheme.
14 comments Labels: cupcake pops
Organ Donors Save Lives!
Organ donors save lives...we hold our fundraising events for Savannah's COTA fund but our deepest desire is that people learn Savvy's story and realize how organ donors truly save lives. Allison and Savannah are here today blessing our lives daily because of the gift of organ donation....Xander is depending on someone to make this decision....no one should have to wait to receive an organ donation. We have learned that our dear Nadia may need a second transplant...our "Hope" child..so you may ask...why do we keep trying to spread the message about organ donation...Savvy has received this Gift...THAT is the reason. We were blessed...Savvy received her Gift and we most honor the decision that our donor angel's family made...we most honor it and pray that others make the same decision...PLEASE if you are not an organ donor...PLEASE consider this amazing Gift...the ultimate Gift of Life. Savannah is a testament to this Gift.
Andrew swimming over 140 laps for his prima!
Happy Birthday Andrew!!! You are an amazing little boy....I am so glad that you remember the day I first got to hold you....I saw this beautiful little baby and when I actually touched you my heart felt so much love that I almost passed out
With Love...
I re-post Sheri's words for she is the mother of Savvy's guardian angel, Antonio. I re-post her words to simply remind us all that what we have is today...we are not guaranteed anything but this moment. If you have a child or have been blessed with more then one child..please remind them daily that you love them...tell them, show them, hug them...never let them go a moment in their lives where they may question how loved they truly are.
www.caringbridge.org/visit/antonioperez
Today marks my 41st Birthday, how I wish Antonio was here with me. My emotions have been out of control and I find no Normal in my life as days go by without you here....
My Normal
From the heart of a bereaved Mother... This is now what "normal" is...
Normal is having tears waiting behind every smile when I realize someone
important is missing from all the important events in my family's life.
Normal for me is trying to decide what to take to the cemetery for Birthdays
Christmas, Thanksgiving, New Years, Valentine's Day, July 4th and Easter.
Normal is feeling like I know how to act and am more comfortable with a
funeral than a wedding or birthday party...yet feeling a stab of pain in
my heart when I smell the flowers and see the casket.
Normal is feeling like I can't sit another minute without getting up and
screaming, because I just don't like to sit through anything.
Normal is not sleeping very well because a thousand what if's & why didn't
I's go through my head constantly.
Normal is reliving that day continuously through my eyes and mind, holding
my head to make it go away.
Normal is having the TV on the minute I walk into the house to have noise,
because the silence is deafening.
Normal is staring at every baby who looks like he is my baby's age. And then
thinking of the age he would be now and not being able to imagine it. Then
wondering why it is even important to imagine it, because it will never
happen.
Normal is every happy event in my life always being backed up with sadness
lurking close behind, because of the hole in my heart.
Normal is telling the story of my child's death as if it were an everyday,
commonplace activity, and then seeing the horror in someone's eyes at how
awful it sounds. And yet realizing it has become a part of my "normal".
Normal is each year coming up with the difficult task of how to honor my
child's memory and his birthday and survive these days. And trying to find
the balloon or flag that fit's the occasion. Happy Birthday? Not really.
Normal is my heart warming and yet sinking at the sight of something special
my baby loved. Thinking how he would love it, but how he is not here to
enjoy it.
Normal is having some people afraid to mention my baby.
Normal is making sure that others remember him.
Normal is after the funeral is over everyone else goes on with their lives,
but we continue to grieve our loss forever.
Normal is weeks, months, and years after the initial shock, the grieving
gets worse sometimes, not better.
Normal is not listening to people compare anything in their life to this
loss, unless they too have lost a child. NOTHING. Even if your child is in
the remotest part of the earth away from you - it doesn't compare. Losing a
parent is horrible, but having to bury your own child is unnatural.
Normal is realizing I do cry everyday.
Normal is disliking jokes about death or funerals, bodies being referred to
as cadavers, when I know they were once someone's loved one.
Normal is being impatient with everything and everyone, except those who are stricken
with grief over the loss of my child.
Normal is sitting at the computer crying, sharing how I feel with chat
buddies who have also lost a child.
Normal is feeling a common bond with friends on the computer in England,
Australia, Canada, the Netherlands and all over the USA, but yet never
having met any of them face to face.
Normal is a new friendship with another grieving mother, talking and crying
together over our children and our new lives.
Normal is being too tired to care if you paid the bills, cleaned the house,
did laundry or if there is any food.
Normal is wondering this time whether I'am going to say I have four
children or three, because I will never see Antonio again and it is not
worth explaining that my baby is in heaven. And yet when I say I have
three children to avoid that problem, I feel horrible as if I have
betrayed my baby.
Normal is avoiding McDonald's and Burger King playgrounds because of small,
happy children that break my heart when I see them.
Normal is asking God why he took my child's life instead of my own...
Normal is knowing I will never get over this loss, in a day or a million
years.
And last of all, Normal is hiding all the things that have become "normal"
for me to feel, so that everyone around me will think that I'am
"normal".
author unknown (some words changed to how I feel)
July 29, 2008
This is going to be a LONG one! How could it not be with the whirlwind weekend we just had...it started off on Thursday learning that Savvy's bloodwork came back out of the "norm"...after hearing from her doctor we chose to go on as planned and took off to Busch Gardens to celebrate our anniversary. On the road we finally were and we see a car in the middle of the road. It took a second to process but oh my goodness a car accident had just occurred and there are people in the car..a woman stumbling out of another car. Super Papi being who he is pulls us to the side of the road and starts running to the cars to help. A few more cars see what is going on and before you know it all of the victims are out of the cars and traffic is re-routed...the police arrive and soon afterwards the fire department...off we go to see the "EEE EEEs" at Busch Gardens.
Friday morning we hop on a very familiar routine going to the airport except for this time we are not heading to CHOP!!! Yeah!!! Savvy is wearing the shirt that Super Papi made for her..."An Organ Donor Saved My Life" and we happily walk through the airport...yup...no stroller this time..the Warrior Princess walked the whole thing!!! It is such a privilege to watch this beautiful child grow up! Savvy loved watching the airplanes pulling in (unlike her Mami...she LOVES to fly!). Well one of the perks to traveling for medical treatment so much in the last year and a half is those frequent flyer miles! Well even Savannah has her own...and they mailed her DRINK coupons...yup...so since she could not enjoy the pleasure of the coupons her Mami enjoyed the vodkas on the plane for her...oh...one does have to enjoy the silver linings! Well...as Mami is ready to go into a nice lull cause the drinkies are hitting her head and we are finally calm and in the air I hear "If there is a doctor or a nurse in the plane please hit your flight attendant button...if you are on the plane simply come to the back of the plane!!"...Okay...so much for the free drink coupons...my eyes are WIDE open...the flight attendant looks VERY nervous and they take out the defibrillator..prayers start...please do not let the person die on the plane....
We sit and wait and the plane lands...the paramedics arrive and take a young girl off of the plane...Thank God she is walking out! Well we ended up getting off of the plane late and that meant we were running late and we are to be at Congressman Van Hollen's office! In D.C. and we are in Baltimore!!! We rush to D.C. (I say this with a smirk since oh...the D.C. traffic has become a NIGHTMARE!). We are now in D.C. and lost for there are barricades all over and we have not driven there in years...we stop at a gas station and ask a nice man for directions...turns out he is heading to the same building! What are the odds (Thank You Guardian Angels!)...this man was so nice...turns out he was a former Congressman!!! Well he had us follow him to this nice neighborhood and park our car for it is impossible to find parking near Capitol Hill. He then drove us to the office ... how cool is he?! So the Warrior Princess got the D.C. Diva treatment...and upon entering the building received her "official" Junior Police Officer badge!
The meeting was wonderful...the question that has been burning a hole in my brain is being researched for me...."Why is organ donation not an Opt OUT program rather then an Opt In?"...oh...if the laws could change!!! So many would be saved the misery of waiting...the misery of being on the brink of death before help can arrive...
The Swim-a-thon
What a wonderful event! Thanks to the incredible generosity of the Belair Swim Club we were able to hold the second annual swim-a-thon for Savvy! My prima , Janid, and Tia Spare Parts, Carolina, who put an amazing amount of work into it last year did it AGAIN! This year the Savoie family joined in the marathon of work!!!
We enter to see a copier, laptop, deejay speakers, "official" Swim-4-Savvy binders...I can not tell you the amount of organization that went into this!! It was an amazing event with blistered feet all over and tired swimmers who swam hundreds of laps!!! There is so much to share ... (and pictures will be coming!)
- The swimmer who swam the MOST laps AGAIN this year is....JASMINE!!!! (What a sweetie!!! She was like a fish who barely left the pool!! Her family along side her supporting her the entire time!!)
- Tom Savoie...STRUTTING down poolside with FLOATIES!!! and when he was not making me laugh with the floaties he was working the Deejay booth...yeah...the DIVA had her own personal 24 hour deejay!! With Hula Girl and I Loved Her First playing!!!
- Our official "Press"...constantly snapping pictures even if it meant climbing walls to get the perfect shot.
- Hanna, Sammy and Bailey who simply kidnapped Savvy and looked for "EEE EEEs" in the trees and plastered a HUGE smile on her face on the swings and swam their little hearts ... I mean HUGE hearts out as well! If I could have kidnapped theses girls and taken them back with me...well...I WOULD HAVE! (Hence, Tom's watchful continuous eye on his daughter!)
- Tents on the ground and sleeping bags from those who spent the night swimming.
- Getting to meet "Thong Man" .. I mean Joe and Jill!!
- Blair and Xander....oh that gorgeous little boy who just melted everyone's heart joining us all day Saturday! What a pleasure to finally meet Blair..the beginning of a long friendship!!! (Xander is another one that would have been kidnapped in a heart beat if we could!!!) I have a bias for liver babies....they are just the CUTEST!!!
- Savannah's first jealousy fit!!! Having Super Papi cuddle with Xander was just too much for her little jealous heart to take!
- Terri, Brian, Allison, and Meghan...what a beautiful family!!! To see Allison doing so well post-transplant...just warms the heart...and I loved knowing that Blair could see Allison and Savvy doing so well...spreading the Hope for Xander!
- Andrew, my nephew, who just learned how to swim...getting his Abuela to sponsor him $3 a lap!!! Abuela thinking he would give up after 5 or 6...well OVER 140 laps later with blistered feet he kept swimming to help his prima!!!
- So many beautiful memories I just have to share them with time for I could type and type and type...
Thank you all of the participants, donors, volunteers for without all of you this would not have been the amazing success that it is!!!!! And Savvy sends lots of "WOV WOV" to her prima Janid, Tia Spare Parts and Tom for the EXTRA hard work you put into it!!!!
July 28, 2008
WOW! What a weekend...I will write all about it tomorrow for we just got home and are pretty tired. Super Papi is off picking up the doggies and Savvy is shoveling her second bowl of pasta into her mouth!!! We have tons of pictures to share .... Savvy in a BIKINI!!!!! But till tomorrow please check out Blair's blog where she has posted some pictures of the Swim-a-thon. Blair is an amazing photographer...but see for yourself.
July 24, 2008
I was ready to cancel everything...but her transplant team has changed Savvy's dosage and she will get labs next week to monitor her levels. She is at a higher risk for infection but they told me to go ahead to Maryland...something I truly appreciate about her transplant team is that they are so keenly aware that the Gift was given so that we may LIVE...not hide. So with precautions in place we will head to Maryland tomorrow...my sister has printed signs and has sectioned off a "safe" space for Savvy at the swim-a-thon and her "liver" friends that will be in attendance. Xander lives in Florida but is waiting for his "call" at John Hopkins so he will be coming to the event and Allison who has received her Gift will also be there...we can not wait to see all the little miracles together! I will update the next blog on Tuesday with pictures of the event.
As an aside...it is official...I am re-admitted into the program...so as of September I will continue my doctoral degree ... I have always teased Robert that the sole purpose for my degree is so that one day I can make dinner reservations under Doctor and MISTER Anselmo.... of course this will not happen for many years to come but I am sure looking forward to making that call!
Today, Robert and I got the most beautiful anniversary gift ever!!! Savvy fell asleep in her car seat and on the way home she was dreaming and saying, "EEE EEE"...no flowers, no fancy dinner, no jewelry could ever top the gift of my daughter dreaming of her fabulous monkeys with a smile on her face...I wanted to buy a little glow in the dark light for her but it seemed more appropriate for an older child and I commented to Robert on how easily I could throw away so much money at a park on Savvy...Robert comments.."she only gets one childhood..and in her case she almost did not get to have it"... and this is why this anniversary like every anniversary from now one is the most special ever! Our Warrior Princess is Here! Thank You Dear Lord for This Beautiful Gift!
As a special favor: Please keep Aiden in prayer tomorrow...Aiden will be in surgery tomorrow to receive a port....here is the update from his site:

http://www.caringbridge.org/fl/aiden/
Thursday, July 24, 2008 8:56 AM CDT
UPDATE thursday night
UHHHH slap me and call me stupid, but I just got Aiden's orders for his IV therapy at home. Uhhh he will not be hooked up once a week or once every 2 weeks.. they want him on 500 cc's of IV fluids NIGHTLY. Every night.
I just am imaginging how my pediatrician will react. (imagine steam shooting from her ears) I am just sitting here thinking.. ok this may change his life for the good.. or this will increase his risk for infection tremendously.
I just have to have faith. I have to have faith. NIGHTLY?
once I am trained.. NO ONE.. I mean NO ONE.. will touch this kid's port. I will be the sole person to hook him up to his IV's. I would rather be responsible of my own child's line that trusting someone else.
I feel like we need some encouragement...
One..
two...
three...
TEAM!
Freaking but FAITHFUL,
Lisa
Team mom
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
previous update
Aiden is ready for his surgery. He knows about it and he says he is ready. Take my word for it.. this only gets more complicated as these kids get older. Now it isn't really about ME and my feelings.. it is about him and still raising him to be a regular kid with some irregular circumstances.
I will say that Aiden's spirits are greatly improved this week. Lots of laughter. I never thought that would decrease in this home, but it did. Steriods can really cause some emotional side effects. So the giggles and smiles are really great to hear and see!
I know this may be a shocker to all those who know me, but Biscuit (the new puppy) has remained a secret still. Yes it is burning a hole in me, but I know it is best to just let the whole thing be a suprise for when the puppy is ready on the 11th.
Anyway, this is just a short update, but I wanted to let you all know the scoop. Suregery is scheduled for 9:30. I believe it will be a 1 hour deal, then recovery (which can vary) He will go to the floor after that and then just rest and chill till Saturday afternoon. Keep him in your thoughts! I am going to go to Blockbuster and rent a new Wii game for when he is home. I saw Wall E there... I think that will be the winner.
Next time I update hopefully it will be to say, "All is well!"
Love The Hawk Family
July 24, 2008
There is a bump in the road today...Just heard from our GI's office that Savvy's labs were not "normal". Her Prograf level is very high so they have contacted CHOP (and of course, I have emailed and called CHOP to follow up) to see what the game plan will be....so we wait to hear.
http://www.netdoctor.co.uk/medicines/100002164.html:
Prograf:
How does it work?
Prograf capsules and injection contain the active ingredient tacrolimus, which is a type of medicine called an immunosuppressant. Immunosuppressants are used to dampen down the activity of cells in the immune system.
When you receive an organ transplant the donor cells, although matched as closely as possible to yours, will not be identical to yours. This means that your immune system will recognise the tissue as foreign and try to attack the transplanted organ. This can result in the transplant being rejected.
Tacrolimus is used to prevent transplant rejection because it suppresses the activity of the cells in your immune system that would normally attack the transplanted tissue.
Tacrolimus acts on the white blood cells. It works by blocking the action of a substance called calcineurin that is found in white blood cells called T-lymphocytes. This action prevents the T-lymphocytes from producing substances called lymphokines.
Lymphokines are normally produced by the T-lymphocytes when a foreign substance is detected in the body. The purpose of the lymphokines is to stimulate the production of more T and B lymphocytes, the white blood cells responsible for regulating and triggering immune responses. The T and B lymphocytes attack foreign invadors and defend the body against infection and foreign cells.
By preventing the production of lymphokines, tacrolimus suppresses the action of the T and B lymphocytes. This stops these cells from attacking foreign invadors and triggering other responses by the immune system.
Tacrolimus is used to prevent rejection of kidney, liver and heart transplants. It is used in combination with other immunosuppressant medicines, such as corticosteroids.
Tacrolimus can be given by mouth or by a drip into a vein (intravenous infusion) if administration by mouth is not possible.
Looking for Volunteers to Help this Weekend in Maryland!!!
We are still looking for volunteers to help on the day of the Swim-a-thon...if you can help please contact Carolina at 240-793-0118.
THE SECOND ANNUAL "SWIM 4 SAVVY" 24 MARATHON IS BEING HELD:
Connecticut Belair Pool
Silver Spring, Maryland
July 26th-27th from noon to noon
Swimmers please click on the link to print a copy of the pledge sheet:
http://www.cotaforsavannaha.com/files/PledgeSheet.pdf
Swimmers please click on the link to print a copy of the registration and waiver form:
http://www.cotaforsavannaha.com/files/RegistrationandWaiverForm.pdf
THANK YOU so very much for participating....Savvy will be at the event cheering you on and giving lots of "Wov Wov"!
*****If you can volunteer at the event or help in gathering donations please contact Carolina at caper213@yahoo.com (Please place Savannah's name on the subject line) or call her at 240-793-0118....thank you~!*****

July 23, 2008 - Pictures!!
We finally downloaded the pictures from our camera so I have posted them!!! Okay...for Simone...the picture of Savvy decked out in her Jewels. For Sam...the picture of Super Papi on his knees in the alligator tunnel...yup...I am risking my marriage for posting that...although I could have picked the FULL tush shot that I got. For Catherine, aka Super Reporter, pictures of our visit in the newsroom...I will email them to you as well...sorry it has taken so long!! For Tia Spare Parts...the bird picture was posed just for you.....no need to explain it to YOU!
For everyone else I do not want to make you mad and have riots starting...I know how you all get!!! YES .. I am talking about YOU Sarah, Sonia, Jen just to name a few so I included her latest doctor visit and her "EEE EEE" visit at Busch Gardens!
As Savvy would say, "WOV WOV" and enjoy!!!
July 23, 2008
Savvy is playing dress up with her princesa jewels on the floor. I got one picture and then the batteries died on the camera so I will ask Robert to download it...she looks serious in it but then being a Diva is a very serious job!
The movie was a BBBBBBBBuzzzt! We went to watch the "Bee Movie" and although she enjoyed every aspect of the movie theater experience the only exception was the actual movie! She loved seeing all of the people and getting compliments from the ticket sales person on how cute she was holding her purse. She did not let go of her little purse the whole morning...I actually had to take it off of her when I took her out of her carseat and placed her in her crib for she fell asleep on the way home.
Savvy became overwhelmed with the Giant Bees....but then again they are 20 times her size and she has never seen anything like it before. Savvy does not normally watch t.v. so from zero to 100 was a bit much. The movie theater was packed with children...guess it is not exactly a "secret" that movies are $1 so there were buses with daycare centers and all kinds of children's groups...I will try to take her again next month ... if she does not like it next time then I will just keep exposing her little by little...she actually did tolerate it for about 15 minutes when I stayed at the end of the aisle by the doors but when I moved towards the screen cause silly Mami was getting tired and wanted to take a seat well she became petrified so we walked around and looked at the movie posters and lights instead of the movie....next month if it continues to be a bust...well life goes on and there is so much more in life to enjoy....such as tomorrow! We are headed to Busch Gardens ... Savvy LOVES it!!! Robert and I are celebrating our 15th wedding anniversary and we can not think of a better way to celebrate it...Savvy LOVES Busch Gardens and we LOVE Savvy...and can not get enough of her Dimples...so I will enjoy my favorite gift of all tomorrow....I will receive Savvylicous Dimples!!!!
July 22, 2008
"She is the quietest blood draw I have"...is what "our" phlebotomist, Julie, said as the Warrior Princess sits on my lap with a needle sticking out of her arm in true Warrior fashion. Julie had her Dora the Explorer stickers waiting for her in the room which happen to match her little outfit. After the needle came out she was not happy...not the "pokey" but the fact that she could not get her food out of the diaper bag...she reached in but couldn't grab it...so like a DIVA she was happy with her shiny beads...I placed two strands over head and she proudly walked out of the room.
Afterwards as a reward (I think the reward was for Mami for she has to wake up super early to get Savvy to the first available appointment...you know the whole deal with having to wait the 30 minutes after her prograf...and not being able to take her prograf until after her labs are drawn...well as a reward for being such a brave girl (Mami)..Super Papi took us to go feed the ducks! and so Mami could drink "liquid gold"..coffee)...oh...the Warrior Princess was going to explode with excitement. The ducks near our church are so use to being fed that they actually come up to the car so Savvy starts shrieking..."Daaahhhhgggg....Dahhhhhggg....aaaattttooooo"...getting I think is Duck to sound like Dog and somewhat of the word in Spanish. Savvy does not get the concept of throwing the bread to the ducks...She wants them to come to her as she holds the bread out for them as our dogs do. So when she could not get them to eat the bread from her hand she offered them dirt and sticks of all shapes and sizes.
Needless to say that when the little Warrior Princess took a nice long nap today and I am sure that the "pokey" was not what she was dreaming of but rather ducks and squirrels all over....although in her dreams they were probably accessorized with the appropriate earrings and necklaces!
Tomorrow we are heading to our first MOVIE!!!! We found a theater that plays children's movies on Wednesday mornings for a $1 and the funds go to charity...I know parents take their kids to the movies all of the time but for me this is an AMAZING first! Whether we stay a minute or an hour it will be fun and I am looking forward to it!
July 21, 2008
My interview went very well .... looks like I will be back in grad school this fall. I will be looking in the mail for my official letter from the school....so what do I want to do when I grow up? For those of you who do not know I was working on my doctorate in clinical psychology when I became pregnant. Savvy and I did our summer and fall semester in 2006 together (of course she was in my belly!)... As we all know life can change oh so quickly so with Savvy's illness many things changed. I had to go on a leave of absence and then eventually drop out of the program. I am a different person now...just can not imagine my exams stressing me out as much as they used to... Today I interviewed for school...tomorrow I hold my daughter as a needle gets placed into her veins and blood gets taken out for the millionth time in her young life...the silver lining in all of this is knowing what is truly important in life.
Speaking of stressing and what is important in life....oh the DIVA! She can not walk by or even get a glimpse of her jewelry box for she starts pointing and shouting "eso..eso"...meaning "that .. that" and wanting you to put her jewels on her...what self respecting Warrior Princess walks around the house without her princesa jewels on? She loves her long pink Cinderella earrings and wants you to tell her "que linda!"...yup she wants you to tell her how pretty she looks and then you get THE DIMPLES!!!! SAVVYLICIOUS!!!!
July 20, 2008
The Warrior Princess is doing great! She still has her runny nose but that is not stopping her from being well...a Warrior Princess! Oh...she is so Yummylicious...can't say it enough.
July 19, 2008
The Warrior Princess is in her jammies and looking absolutely adorable!!! It is the kind with the feeties...just love them!! We are waiting until 8 so that she is able to drink her milk and head to sleep...she is playing with her musical chair and dancing just too cute! She has been OBSESSED with her new fancy dancy princesa jewelry that Simone mailed her. She has a beautiful little jewelry box with her name on it and Disney Princess JEWELS!!! YUP!! JEWELS...the kind that make a little girls eyes POP out when she puts them on...she has been strutting around with her big JEWELED pink plastic princesa earings and shaking her head so she can feel them...and we can not be a true princesa without wearing the matching necklace and bracelets!!!!
***********************
Okay, I had to stop typing for the princesa needed to change earrings several times and then of course the bracelet has to change...you know the diva drill. She is in bed but not asleep yet...she has her runny nose back and this time...I have decided to join her. I am sick today...started last night but that is not to detract from the horrible "Death Bed" sickness that her Super Papi has...you know His sore throat and other symptoms are WORSE then anyone has ever experienced and how he manages to walk around is beyond me (I say mocking him).
Savvy had a great time today...we had to head out to the mall this evening for I needed a pair of shoes (yup...I have a shoe thing and had an amazing collection of shoes...well...until my feet GREW after my pregnancy...go figure!) and since I have lived in flip flops and sneakers for the past year I do not have a pair of heals that actually fit me and I have an interview for school on Monday morning. ..don't think they will like the flip flop "look"... I have re-applied to my doctorate program...wish me luck! Well, Savvy LOVED going to the mall...there is a carousel in the middle of the mall and I always wondered what sucker parents would pay to have their kid ride a carousel in the middle of a mall....well....I welcome myself to the "sucker parent club"...can not help myself...she saw the horses and started to point and clap!!! How can one resist the dimples???
We then enter Macy's to check out the sale they were having and here is my little girl heading straight towards the purses!!! She was in purse heaven and of course...she has expensive taste for she did not want to leave the Coach counter....did I mention diva???? Okay....for those who might ask...NO WAY did she walk out with a purse ... I just give in to carousel rides...but it was truly to cute! I think we may be in a whole heck of a lot of trouble in the teen mall shopping years...
Super Papi snuck into her nursery...I hear the giggles....yup...so much for the sleeping princesa....
So this time next week we will be in Maryland....Savvy has the cutest little bikini ready to show off! Gotta show off our beautiful Warrior Princess scar! We thank our beautiful donor family for this....for last year I remember the swim-a-thon going on and wishing that Savvy were not so sick as to be able to attend...but we were so afraid to even let her out of the house and expose her to people...last year we were not sure if she would be alive at this time...and here she is today...enjoying carousel rides at the mall and wearing her fancy plastic princesa earrings...without our Gift...I do not even want to imagine it...please remember that there are many still waiting for this amazing Gift of Life. Share Savvy's story with a friend, an acquaintance...let them know that the decision to become an organ donor REALLY does save lives..please leave this legacy.
As per unos.org:
Waiting list candidates
| 99,418 | as of today 8:23pm |
July 18, 2008
Oh my goodness it is Friday! Where did this week go??? I was putting Savvy down for her naptime and I realized that I had completely forgotten that today was Friday! Well, I took a little break from the computer...just felt I was getting on way too much and needed to "cut the strings" for a bit on my computer "addiction!" so I have not updated...but things are going well!
Savvy had a runny nose and cough but nothing the humidifier could not solve...she is back to 100% again...wearing her oatmeal in her hair. Super Papi...not doing as well..he has been sick the past few days...or on his "DEATH BED" as one might think by listening to his moaning and groaning when his wife is in ear shot.
I had my heart skip a beat this week when I learned that our letter to our donor family had been approved and forwarded to them by Gift of Life. I was naive to think that they had already received it and had not wanted contact with us just yet but I have learned that they have not even had a chance to read it yet since the process seems to be pretty slow going...I pray that I wrote the right words in expressing our deep gratitude to them.
Next week we are off to the swim-a-thon in Maryland....we are heading to Capitol Hill on Friday thanks to Tom Savoie...meeting his Congressman....another wonderful scrapbook moment...but I confess that I am more excited to meet Tom and his family!!!! Any man who is willing to put floaties on is super cool in my book!
If you are in the area please stop by and visit us..."wov wov" to all!
July 14, 2008
Super Papi is at the vet with Lucky..poor thing has some pee pee problems...you know in our house we are all about the bodily functions! The Warrior Princess traumatized her father this morning with her bodily functions....I believe the quote was "after this one I don't think I should have to change another one for a year.."..(here is where you insert me mocking my husband...mocking...still mocking....)
My Warrior Princess is up full of energy playing with her toys....thank goodness I got my class of liquid gold (coffee) in my system already! I am typing and playing peek-a-boo on the laptop and she is giggling so loud as if this were the funniest game ever! She is so cute it is ridiculous!
I freaked out my sweet baby last night....I have to share this as to share Robert's great parental quote. I cut myself and put a paper towel on it....the towel had what appeared to be a lot of blood because it spread...Savvy saw me with the paper towel in my hand and the blood and to my surprise starting crying....I mean sobbing in a panic (my heart broke for I realized that she knew it was blood). I told her it was okay and showed her how Mami was fine and calmed her down...so when I told Robert about her reaction and how sad it is that at her age she knew that something was "wrong" cause of the blood on Mami...he tells me "well she showed empathy...that means she is not a sociopath and that is good!"....how could I not share this qoute?! So to console me, my husband points out that my child is not a sociopath....yup....guess we should get some kind of parental award for this!
Speaking of parental awards....one should go to my brother, Ozzie, and sister-in-law, Pattie, for baking one of the cutest little chunky monkeys ever! Savvy's primo, Presley, turned ONE yesterday!!! He is so darn cute!..but then so are his brother and sister!
*** Presley *** Feliz Cumpleaños Mi Amor!!
Estas son las mañanitas, que cantaba el Rey David. Hoy por ser día de tu santo, te las cantamos a ti.
Despierta mi bien despiertam mira que ya amaneció. Ya los pajaritos cantan. La luna ya se metió
Que linda está la mañana en que vengo a saludarte. Venimos todos con gusto y placer a felicitarte.
Ya viene amaneciendo. Ya la luz del día nos dio. Levántate de mañana. Mira que ya amaneció.
July 10, 2008
"EEEE EEEE"...."EEEEE EEEEE"...can you imagine the excitement on Savannah's face when she realized that "EEE EEEs" come alive?! After nap time we took our Warrior Princess to see the new Jungala exhibit at Busch Gardens (Yeah for season passes!).. she was FASCINATED with the orangutan exhibit! Monkeys just like her climbing around and then one actually went to a hammock underneath her feet (it is a glass enclosure)! If Savvy could have jumped into the exhibit with them she would have!!! She also loved the alligator tunnel....YUP...Super Papi took her in there...it was the height of Savvy so Super Papi had to crawl in (I have great pictures of his tush next to his princesa on his hands and knees with a gator above his head...oh what that man won't do for his girl!
I am glad she enjoyed the gator tunnel cause we all know she won't be visiting it with Mami! No Way!! On the way home...Savvy could barely keep her eyes open and we could hear in the car seat with "her EEE EEE" saying..."EEE EEE"..."EEE EEE"...it was precious!
As for her shots...we have seen no side effects at all!!!! Wooohoooo for the Warrior Princess!!
July 9, 2009
The Warrior Princess has had a great morning. She went to visit her friends at the St. Pete times office...yup...her "personal "photographer (Skip) and reporter (Catherine) ...the life of a diva! and we got to meet their co-workers and the "Big Bossman"...whose office Savvy simply wanted to move into...yup...she is all about the corner office!
Savvy loved her first internship as a writer for the St. Pete times...she pounded away at the keyboard and visited graciously with her future co-workers....apparently she needs to learn how to spell before they will consider an "official" internship position...it was a super nice visit and Savvy could have not been happier then to walk away with new beads for her collection...yup...she got the fancy Times beads!
We had to leave and head over for a wellness appointment which meant .... SHOTS! We had camera in hand ready to take pics with Dr. Wonderful but unfortunately we did not get to see her due to an emergency (I think she heard we were bringing a camera)...we had a nice visit with another doctor and Savvy is progressing very well...funny thing is that Savvy's head is large and I wandered why the large difference between the percentile of her weight, height and then head....his answer .. "usually this is seen due to familial patterns..."...I had to laugh and thanked him...told him that I appreciated him not saying ..." it is because her Mama has a large head...duh!"...I liked his answer so much better!
Well, we were all good until the shot time...and then like any other child Savvy lost it...the nurse was super fast. She took 4 shots on her legs and Savvy was in my arms in seconds but I know that Savvy would probably argue and tell you it felt like hours.
So, things are looking good! We continue to be blessed with a "healthy" child. We have plans to be in Maryland at the end of the month for the swim-a-thon and thanks to Tom (Hannah's dad) we may be heading to Capitol Hill....that is exciting and something we look forward to!
July 8, 2008
Well technically it is the early hours of July 9th but since I did not write earlier I thought this would count for the 8th....I was going to write and actually did but then deleted the post....it wasn't til Robert got home from work and asked why I was so angry that it hit me that I should write about it and get it off my chest. Here it is. Someone stole Antonio's frogs from his grave site. I am disgusted by this ...how any one can look at Angel Antonio's picture which is on his tombstone and steal his frogs. They are not just frogs .. they are an expression of love from his family for a child who simply LOVED frogs. It made me sick to learn this and then to learn that Sheri as heartbroken as she is .. is ready to forgive the perpetrators of this disgrace...that just leaves me in awe of the human spirit....to be heartbroken and yet turn around and forgive stranger who were so cruel...this is probably why Antonio's spirit is so beautiful and strong ... he is a child of pure love.
So I spent my day angry and had a hard time snapping out of it...probably because there was nothing I could do about it. I wish I could get the frogs back but I know that I can not. So, I send this little picture of an angel frog to the Perez family and to our sweet Antonio..I know it does not replace the frogs that were taken but I do send it with love!


****************Swim 4 Savvy*******************
THE SECOND ANNUAL "SWIM 4 SAVVY" 24 MARATHON IS BEING HELD:
Connecticut Belair Pool
Rockville, Maryland
July 26th-27th from noon to noon
Swimmers please click on the link to print a copy of the pledge sheet:
http://www.cotaforsavannaha.com/files/PledgeSheet.pdf
Swimmers please click on the link to print a copy of the registration and waiver form:
http://www.cotaforsavannaha.com/files/RegistrationandWaiverForm.pdf
THANK YOU so very much for participating....Savvy will be at the event cheering you on and giving lots of "Wov Wov"!
*****If you can volunteer at the event or help in gathering donations please contact Carolina at caper213@yahoo.com (Please place Savannah's name on the subject line) or call her at 240-793-0118....thank you~!*****

July 7, 2008
"Mas....Mas" is all I heard this morning...the W.P. "WOVS" her food! "Mas" means "more" in Spanish but Savvy uses it only when asking for food. Super Papi usually prepares her a waffle and oatmeal in the morning but this morning he headed to work early and I made the mistake of giving her a waffle and rice milk....thinking that it would be plenty for this tiny little princesa....and boy was I wrong! "Mas...Mas...Mas..."... she makes it VERY clear when she is not "all done". I am just writing about it so I can look back on my journals when she is older and smile at her cute little sayings.
Speaking of cute...I had mentioned that the day we went to the ER a few weeks ago from a GI bug Savvy had received a package from Simone (Angel Lisa's mom)...the timing was amazing because in the middle of the night when we got home she just sat up and played and played (she had 2 bags of IV in her and anti-nausea drugs making her feel better!) This toy is a large sand and water toy with an umbrella and boats...super cute. Savvy had been playing with it inside up until yesterday when Super Papi took it outside and filled it with water....so now all of her toys FLOAT! Oh this cutie patootie was so excited to splash the water and get herself all wet. When we tried to pull her away so we could go back inside she sat down and did everything in her power not to let herself be pulled from her toy. I had never seen anything like this before...Robert and I were like "oh oh...we are going to break her heart because we can't leave her in the yard until she goes off to college playing with her toy..." then we got smart...yup...I am patting us on the back for the genius parenting skills that all of a sudden were sent to us from the joo joo gods above! We had Savvy help us pour out the water and put her toys away and help Super Papi pack it up in the garage! Ohhhhhhhhhhhhhh.............it was so cute to see her get so serious about making sure everything in her wonderful paradise was placed in the right section....so cute! Again, I share this for myself for I simply do not want to forget the look on her face.
Today, another memory that I want to write down is the little W.P. with her Mr. Potatoe Head...she has had him for awhile in her closet. It was a gift that she won at the Easter Egg hunt...an Easter Bunny Mr. Potatoe Head. I felt that it had to many smaller parts for her at the time so I placed him in the closet and periodically she goes into the closet and takes him out and looks at him...today, she took him out and I took him out of the box for her...she was sooooo excited and spent the rest of the morning walking around with this Mr. Potatoe Head with Easter Bunny ears as if it were her new best friend. She even wanted to cuddle with him while she drank her milk before naptime but I just had to switch him for her teddy...but she kept Mr. Potatoe Head within eye shot....just too cute.
Okay....I think my little girl is cute! Surprise?!
Oh....and I do have to share that I got an email from my friend, Allison, (Savvy's future Mommy-in-law) and I have to share a portion of it....for she did point out that my baby is 19 months and not 18 months....Robert and I laughed our tushes off when I got it! Yeah....I typed in 18 rather then 19 but I am tickled to see that you are reading up on your future princesa-in-law! Soooooo...........yeah....my little girl is 19 months old....on my 19th "first official date" anniversary!....it is "first official date" anniversary because I did sneak out to meet Robert on the 4th of July...but that is another story! (Moral of the story for the day....NEVER ban your daughter from seeing a boy....for they may simply turn around and marry him!)
You, My Sisters
You, My Sisters
By Maureen K. Higgins
Many of you I have never even met face to face, but I've searched you out every day. I've looked for you on the internet, on playgrounds and in grocery stores.
I've become an expert at identifying you. You are well worn. You are stronger than you ever wanted to be. Your words ring with experience, experience you culled with your very heart and soul. You are compassionate beyond the expectations of this world. You are my "sisters."
Yes, you and I, my friend, are sisters in a sorority. A very elite sorority. We are special. Just like any other sorority, we were chosen to be members. Some of us were invited to join immediately, some not for months or even years. Some of us even tried to refuse membership, but to no avail.
We were initiated in neurologist' s offices and NICU units, in obstetrician' s offices, in emergency rooms, and during ultrasounds. We were initiated with somber telephone calls, consultations, evaluations, blood tests, x-rays, MRI films, and heart surgeries.
All of us have one thing in common. One day things were fine. We were pregnant, or we had just given birth, or we were nursing our newborn, or we were playing with our toddler. Yes, one minute everything was fine. Then, whether it happened in an instant, as it often does, or over the course of a few weeks or months, our entire lives changed. Something wasn't quite right. Then we found ourselves mothers of children with special needs.
We are united, we sisters, regardless of the diversity of our children's special needs. Some of our children undergo chemotherapy. Some need respirators and ventilators. Some are unable to talk, some are unable to walk. Some eat through feeding tubes. Some live in a different world. We do not discriminate against those mothers whose children's needs are not as "special" as our child's. We have mutual respect and empathy for all the women who walk in our shoes.
We are knowledgeable. We have educated ourselves with whatever materials we could find. We know "the" specialists in the field. We know "the" neurologists, "the" hospitals, "the" wonder drugs, "the" treatments. We know "the" tests that need to be done, we know "the" degenerative and progressive diseases and we hold our breath while our children are tested for them. Without formal education, we could become board certified in neurology, endocrinology, and physiatry.
We have taken on our insurance companies and school boards to get what our children need to survive, and to flourish. We have prevailed upon the State to include augmentative communication devices in special education classes and mainstream schools for our children with cerebral palsy. We have labored to prove to insurance companies the medical necessity of gait trainers and other adaptive equipment for our children with spinal cord defects. We have sued municipalities to have our children properly classified so they could receive education and evaluation commensurate with their diagnosis.
We have learned to deal with the rest of the world, even if that means walking away from it. We have tolerated scorn in supermarkets during "tantrums" and gritted our teeth while discipline was advocated by the person behind us in line. We have tolerated inane suggestions and home remedies from well-meaning strangers. We have tolerated mothers of children without special needs complaining about chicken pox and ear infections. We have learned that many of our closest friends can't understand what it's like to be in our sorority, and don't even want to try.
We have our own personal copies of Emily Perl Kingsley's "A Trip To Holland" and Erma Bombeck's "The Special Mother." We keep them by our bedside and read and reread them during our toughest hours.
We have coped with holidays. We have found ways to get our physically handicapped children to the neighbors' front doors on Halloween, and we have found ways to help our deaf children form the words, "trick or treat." We have accepted that our children with sensory dysfunction will never wear velvet or lace on Christmas. We have painted a canvas of lights and a blazing yule log with our words for our blind children. We have pureed turkey on Thanksgiving. We have bought white chocolate bunnies for Easter. And all the while, we have tried to create a festive atmosphere for the rest of our family.
We've gotten up every morning since our journey began wondering how we'd make it through another day, and gone to bed every evening not sure how we did it.
We've mourned the fact that we never got to relax and sip red wine in Italy . We've mourned the fact that our trip to Holland has required much more baggage than we ever imagined when we first visited the travel agent. And we've mourned because we left for the airport without most of the things we needed for the trip.
But we, sisters, we keep the faith always. We never stop believing. Our love for our special children and our belief in all that they will achieve in life knows no bounds. We dream of them scoring touchdowns and extra points and home runs. We visualize them running sprints and marathons. We dream of them planting vegetable seeds, riding horses and chopping down trees. We hear their angelic voices singing Christmas carols. We see their palettes smeared with watercolors, and their fingers flying over ivory keys in a concert hall. We are amazed at the grace of their pirouettes. We never, never stop believing in all they will accomplish as they pass through this world.
But in the meantime, my sisters, the most important thing we do, is hold tight to their little hands as together, we special mothers and our special children, reach for the stars.
July 6, 2008
"WOV...WOV"..... now picture those cute little words being said by the cutest formerly yellow, dimple faced girl that you have ever seen....absolutely YUMMILICIOUS! Yup...now she will wave "Bye Bye" and tell you she loves loves you! YUMMMMMMMMMMMMMMMMMYYYYYYYYYYYYYYYYY!!!!!!!!!!!!!!!!!!!!!!
Yesterday Robert and I celebrated our "anniversary"...yup of our first "official" date ....19 years ago.........where does time go? What better way to celebrate it then to have our baby girl turn 18 months!!!! How amazing is this? This time last year we were not sure if our yummylicious little baby would be here to celebrate another birthday but because of her donor angel's family...she is going strong...saying "WOV WOV" and melting our hearts each and every day!
She is even adorable when she is placed in "time out"...yup....Super Papi or I will count "1, 2, 3" and repeat no to her for whatever she is doing that we do not like...then at 3 she usually has this little look of "oooohhhh oooohhhhh" I better climb off of this toy and listen but then it is too late so she has to go to "time out"...she stands in the corner and then when you ask she will say "ori.." her version of "sorry" and then a great big hug because we "wov wov" each other and then we can go back and play...seriously....this kid is so cute I almost can't stand it!
She was a busy little girl this holiday weekend...she went to Super Papi's office and helped him "work" and "organize"...she has "her" administrative assistant drawer so she keeps very busy. Then we went to the park which she LOVES! Super Papi has a great park by his office...oh...and we can't forget how her eyes popped out as we fed the ducks...I am sure she dreamt about that! She simply reminds us of how lucky we are on a daily basis.
We have been so blessed...blessed on a daily basis...and we are so grateful!
*****************
So many wait for the precious gift that we have been granted. If you are not already an organ donor please consider doing so. If you are an organ donor...please let your family know. You are not too young...or too old...or too unhealthy...or too.....become one and let the doctor's decide who can benefit from your amazing gift...leave a legacy ... a legacy of life.
Today so many wait...it is not just a number ... these are individuals...people...loved ones...brothers...sisters..babies...Mami's and Super Papi's...
As per unos.org:
Waiting list candidates
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99,245 as of today 12:59pm
Happy 4th!!!Wishing everyone a Happy Fourth of July! We hope you have a fabulous, fun and safe holiday weekend!!! July 3, 2008Submitted by Robert on Thu, 07/03/2008 - 12:16pm.
It was a tough night for the President of the Super Papi fan club...Savannah is napping along with Super Papi since they were up all night together (Bless his heart he let me try to sleep through it) ...not sure what is going on with her right now but she is super fussy and whiny and waking up screaming which is not typical for her (at least not recently)... We are going to wait until she wakes from her nap and then call Dr. Wonderful to let her know Savvy's progress. *********************************** The President of the Super Papi fan club woke up with huge dimples on her cheeks since Super Papi was in the chair next to her crib...which is how every princesa should awaken...with her Knight in Shining Armor standing guard...and her pink stuffed "EEE EEE" under her arm. Savvy seems to be doing better...she is eating her Cheerios as I type...hopefully this is all just a normal kid thing.
Needing a Donated Space in Brandon/Riverview/Apollo Beach AreaSubmitted by Robert on Tue, 07/01/2008 - 12:32pm.
I am need of a space to hold this years scrapbook fundraiser....if you know of anyone who could help us with this please contact me at analiz0211@yahoo.com...it can be any type of space...a warehouse space...a hotel area...the clubhouse...use your imagination..it just needs to hold scrappers and tables... This year we are excited to say that we are teaming up with Scrapbook Royalty for the fundraiser!!! ( www.scrapbookroyalty.com )
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