One step at a time.....

Just a little update.....I promised to try to do better at keeping her blog updated, although, there really isn't anything new or exciting happening.....but, I have to believe in my heart that we are moving forward.

Every day, we continue to battle pain and "phantom" fevers....we've done lab after lab, and while some things come back "abnormal", nothing seems to give us any clear cut answers.  Some days are better than others....she has really good days, where she walks, run, jumps and plays....and, you can't imagine how it warms my heart to watch her do so.  The downside is that those days always come at a price.  Within hours, her pain is.....almost consuming.  Fevers always seem to follow suit.  Her pain/fever reducing meds help, but, not for long.  They are a "band-aid" we use....it helps the symptoms, but we are praying to eliminate the cause.  Rheumatology still sits as a "maybe"....and so, the circle continues.
Yesterday, she woke up feeling pain, and looking more pale than usual, and a couple of times, she said she was dizzy.  When we took her for her blood work around 1:30 or so, I noticed she felt warm.  I had no thermometer to check her, and she had no other symptoms other than the pain.  She was amazingly brave and strong, and didn't shed a tear as they stuck her.  We did our usual mantra...."What do we say, Mia?"...."No Fear, Mamma!"...."that's right, baby....why are we not afraid?"...."Because, Jesus is with me!".....;)   If nothing else, she knows the most important one to turn to....in times of joy, times of pain, times of celebration and times of fear.  This alone comforts my "mother's heart"...
Within 5 minutes of completing the blood draw, she started to look strange....next thing I knew, she had vomited all over herself, Daddy, the tech, the floor....just everywhere.....more color drained from her face....we get her settled, and her little legs were so wobbly, she couldn't stand.  Was it the blood draw ??  the fever ???  the pain ???  Truthfully, we don't know !!  After a few hours, she seemed better....was a little relieved the pediatrician didn't call back...would have felt silly saying "she's ok now"....still we need to find out why these things keep happening, and so randomly.  She slept well last night, and today seems...well, what has become more the norm, for her.

I know and believe in my heart that we will get her through this.....we will find answers, and we will continue to fight until we do !! As we all heard and learned in my last post....we fully intend to "Finish the Drill"!!!! ;)

Please continue to pray for Mia and for her doctors and all who love and look after her......pray for our strength, courage, faith, determination, healing and comfort while we seek answers.  And know, beyond a shadow of a doubt that Team Mia is prayed for daily !!!!! ;)

Thank you, for loving us through it all......and thank you, thank you, thank you for choosing to be a miracle for our Mia, and know that we will not give up on our fight....we'll continue to take it, one step at a time !!!!!!!!!!

We love you all !!!!

With a Mamma's very grateful heart,
~ <3 Gina <3 ~

Sunday, May 12, 2013 - Mother's Day....feeding the goats at Southern Belle Farms, McDonough

Picking some fresh strawberries at the farm !  We had to sit, "just for a while, Mamma"   this child is my heart !!! 

Live life, have faith and “FINISH THE DRILL!”

You might want to grab a cup of coffee….this post is going to “take a minute”… ;)

Soooo….who’s mad at me for not updating ??!! [hanging my head in shame.]   I’m sorry…I truly am.  I have been a little overwhelmed, as we have been dealing with a series of….not really “setbacks” so much as problematic “snags”.  For the past several months, Mia has been contending with an unexplained increase in pain as well as random high fevers.  When she has a ‘flare up’, she spends about a week in bed until it passes.  We are working closely with her pediatrician, her surgeon and now a rheumatologist to get some answers.  We are trying to figure out if it is related to her hip dysplasia.  We are blessed to have these people as well as all of you on our “team”….Team Mia.  And, do not worry, God is in control, and I promise to do better at keeping her blog updated with what we find !!!   ;)  Never for a moment am I ever NOT grateful for your love and prayers!  We all are.  ;)

Now, while we are on the subject of “teams”, I want very much to share something with all of you.

Here in the USA, American football is very big….REALLY big….particularly on the College level.  I am not pointing any fingers, since I myself have a love for the game.  I grew up in a football family….my Dad coached, my brothers played, my Mom gave of her time/talents as a team Mom, and I cheered.  I have a respect for team sports which my Dad shared with us…many things you need for life can be learned in playing a team sport.  Things like teamwork, respect for authority,  determination, perseverance, endurance, humility.   (Yes, humility….take a string of losses and it will save you from an ego swell!  Haha)  So, while I’ve never actually played the game, I ‘get it’, I love it, I watch it, I learn from it! And, while neither my husband, nor I ever attended the University of Georgia, we are very much “Dawg” fans…both my Michael and I have family members who have graduated from UGA, and…well, once a GA family, always a GA family !!!  ;)

While I have followed GA football for many years, and I have always had a healthy respect for past players and Coaches….I have a confession….none have touched my heart as much as our current Coach, Mark Richt has.  I have not met him personally, but I have yet to hear from anyone who has met him that he is anything other than a genuinely good man.  I think it is probably his courage to share his faith that first made me pay attention when he talked.    With his permission, I want to share with you 3 little words, with 1 BIG message!  “FINISH THE DRILL”.  These are the words God gave Coach Richt to use to motivate his players and the other students….little did he know that God would use him and his words to motivate many others beyond the football field.  Myself included.  When I first heard those words, “Finish the Drill”, I had just begun a personal battle to lose weight.  (they helped and I did….but, that’s another story for another day !! haha)  That phrase resonated within me.  “Finish the Drill”.  When Mia was diagnosed with her hip dysplasia, again they surfaced, and in my heart I heard, “finish the drill”.  We were given a brand new “drill”.

 By its definition, a “drill” is (according to the online dictionary), “A task or exercise for teaching a skill or procedure by repetition.”  And, here’s the important, critical thing….in order for a drill to be effective, you must have a GOAL !!!  What is your goal?  What are you working towards? 

My earthly goal is simple.  To have a happy, healthy little girl who can live, love and enjoy her life while glorifying God through it.  For me to reach my goal it will take many drills to build my faith and to teach my Mia.  And, in His infinite wisdom, God will allow me (and you!) to do it again and again and again until we get it right, and it becomes a part of our very nature.  I’m grateful for this!  So, so grateful.  

On the surface, drills can sometimes seem pointless…and, they are exhausting! However, a specific drill is used in a specific situation to develop a specific attribute or ability.  A drill done hard enough and long enough will rock you to your core, and make you reach into a place deep within your heart and soul to find the strength to finish it. (Football players everywhere are shaking their heads in agreement right now!  hahaha…”death crawl”, guys ???!! hahaha ) Drills can lift you up, and take you to a higher place if you let them.  That is what they are designed to do!  That is their purpose!  They ‘invade’ you, they permeate your being, mold you and push you to greatness.  

And, let’s face it, the old adage is true, ‘anything worth having is worth working for.’

“Finish the Drill” means, knowing what (and who) you are fighting for and not losing sight of that.  Despite how tired you may get….how many ‘blows’ you may take…how many setbacks you may have.  You must start strong, stay strong, and finish STRONG!  And, you can do this, because He promises to do it with you!  He, God, is our Coach.  He will lead us and guide us, encourage us and push us, because in the end that is what a good Coach does, but more importantly it is what a loving Father does.  He hand- picked each of our drills…knowing the best one to develop in us what we would need to accomplish our goal.  He has picked yours too.  Whatever your “field of battle” may be….whether its hip dysplasia, some other illness, an addiction, a hurting heart….He knows.   I promise you, He knows.  And, He is with you, always!  Will it be easy?  No.  Will you get tired? Yes.  Will you want to give up?  Absolutely!…..  Will it be worth it?  YES!!!!

I found an article recently, where Coach Richt talks about his job, and he is quoted as having said, “…I couldn’t do this job without His [God’s] strength, power, and wisdom. We all have a limitation to our knowledge and our strength, our stamina—whatever it is, we all have limits. Once we hit the limit, if we have nowhere to turn, that’s when we have despair and depression. But if we know God is there for us and we are connected to his power, we can keep going.”   This statement is true in coaching… true in football....true in every, single aspect of life.  If God didn’t believe you could do it, He never would have chosen you for the job.  He does not ever set you up to fail.  He says, “A thief comes only to steal and slaughter and destroy; I came so that they might have life and have it more abundantly.” John 10:10

The field of hip dysplasia is an ugly place.  Particularly here in the last few weeks, it has felt especially rough.  Unfortunately, we have new people, new children taking the field for the first time, just beginning their fight.  We have some who are deep within the 4^th quarter.  Others, like ourselves, are praying and waiting to hear the buzzer to signal that we’ve at least made it to half time.  And, as I look around at my teammates, many of them are beaten and bruised.  They are weary, and frustrated.   And, we are all so very tired.  So now, NOW is the time for you to reach within.  Now is the time for you to dig deep and find within yourself the courage to continue.  As one of my most favorite lines from one of my most favorite movies says, “…it’s all heart from here”.  (Facing the Giants….if you haven’t seen it, check it out, and you will LOVE this scene !!!)  Make the choice!  Choose to fight!  Choose to keep going!  In time, you will win!

Know that throughout your battle, God will pick drills especially for you, yes, and sometimes, you will win….sometimes you will lose.  How many W’s or L’s you have aren’t nearly as important as the amount of heart with which you fought, the experiences you drew from having fought, and the people you touched along the way.  He will also give you incredible teammates, people who share the same ‘field’…those who will fight with you.  Just remember to look around….. You’re not alone….not only are there teammates for you to rely on….there are many who are cheering you on, and your heavenly “Coach” and Father will never let you down!

Whatever the battle, fight hard and fight smart!  

Remember to:

Protect your mind….do not allow things like doubt, fear and anxiety to take root and set up residence.  They will deter you from your goal, and interrupt your drill.  Exercise your knowledge!

Protect your words…..words have power!  What you say, you will bring in to existence!  If you say you “can’t”, then, you “won’t”….it really is that simple.  Choose to stay positive.  Exercise your will!

Protect your heart….safeguard against despair and depression.  They have no place in a fighter like you.  Exercise your hope!

And, protect your Spirit…..it is where God dwells with you, and in you, and through you.  Exercise your love!

I want to thank Coach Richt for allowing me to share his ‘motto’ with all of you.  I am grateful for the encouragement and strength I have received from them, and since they are words which I believe have been inspired by God, I hope that you will find in them the strength you need to look deep within and find whatever tools you may need in your personal battle.

When you get tired….when you feel you can’t take another step…when you feel that you are losing hope, remember…..I believe in you….I believe in the one who made you….I know you can do it !!!

Now, go….live life….have faith…….and FINISH THE DRILL !!!!!!!!!!!!!  ;)

Oh, and lest we forget…….GO DAWGS !!!!!!!!!!!!!!!!!! ;)

With a Mamma's grateful heart,
~Gina

Love & Hope the Hip Hippo !!

Greetings one and all !!!! ;)

I owe everyone such an apology for not having updated Mia's blog !!!  I do apologize !!!!
Mia had her second surgery back in March, and well....the honest to goodness truth of it, is that her second surgery was just sooo ugly, that I really couldn't make myself write about it.  Now, after much prayer and having plunged myself into several others projects, it's better.  It doesn't upset me as much, mostly because I see my blessings.  I'm choosing to focus on those !!  So, a condensed version of her second surgery (and,  pleeeease use this information to make yourself aware of what is out there, I believe knowledge is power, even if the knowledge is scary, and ugly !!...but, whatever you do, please do NOT think or assume that what went on with Mia is what will happen with your little one !!!!!!!!!! Every child and every ddh is unique, and Mia's case just happens to be one of the more severe.)
Before I share, I will tell you that Mia is doing AMAZING !!!!!!! ;)
Her second surgery caught us all off guard.  The time in between surgeries, while not long (and she was pretty much immobile), proved problematic, because it gave her left femur time to "drift" farther up.  By surgery time, her left femur was well up under her ribs.  Apparently, you (the surgeon) only has so many 'chances' to get the hip in, before it is rendered pretty much useless.  Our amazing surgeon spent those quickly.  He was then faced with a choice....leave her hip out permanently, or "take out her left leg"....after much soul searching, he made the VERY difficult choice to take out her left leg, because he truly felt in his heart that doing so would be temporary, and would prove best for her over-all quality of life.  To "take out her left leg", meant that he paralyzed her.  I saw the pain in his eyes as he explained it to us....I knew how hard this choice was for him...but, I also knew that my baby was paralyzed.  A lot to process.  He warned us the paralysis could take years to go away.....GOD IS AWESOME, and on day 6 post-surgery, Mia moved her big toe !! Today, Mia's paralysis is 100% gone !! ;)  While we were still processing the paralysis, we jump to day 2 post surgery....this is when Mia began to 'crash'....all of her vitals were just.....well, she was in real trouble !! They called for an immediate transfusion to save her.....after tears, praying, biting fingers nails, (and I think, quite truthfully I may even have been physically sick) she responded to the transfusion, and recovered.  Near death will definitely put perspective on paralysis....I remember thinking..."just save her....I don't care if she can't walk....I need her here with me....just leave her with me!"....we knew surgery ran risks....all surgery does....we are just so grateful.....so..soooo grateful that surgery #3 (technically it was her 3rd, since her 2nd was a cast change/arthrogram) is behind us....so grateful that Mia is back to walking, running, jumping, playing and dancing....so grateful for so much !!!  We consider that surgery a great success.  Yes, her legs are still different lengths, and always will be....yes, she still walks with a "swag" and a little limp....yes, she still has pain....however.....the pain is soooooooooo much better than where it was, as are the swag and limp !! She's getting there, and she'll be better than ever !!!! We take her back into surgery in February to remove the metal in both legs....then another surgery for 'tweaking' a year after.  Hip dysplasia  is not quick run....it is in fact a 'marathon', and you must pace yourself taking one step at a time !!! ;)
One of the projects I have poured myself into as my way of working through things is the new book.  I firmly believe that all of the anger and frustration I was feeling needed to be channeled....it needed to be put to some good use so that it didn't not consume me or my family.  What better way than to channel all of it back onto hip dysplasia !!!  Let's take all the ugly and use it for something good and positive !!! Let's help other Mom/Dads & little ones be a little less afraid of the road ahead....let's make a road sign....let's help point the way.....let's spread some hope..... ;)
And, so....after almost a year, Hope, the hip hippo was born !!! ;)  She is a sweet little hippo, around 3 or so, so very much a toddler, who is diagnosed with hip dysplasia.  The book takes her through her diagnosis, surgery, casting and recovery and I am so proud to say has been very well received !!!! To hear how Hope is helping to explain things to the little ones....help Moms & Dads understand what they may be up against, as well as help siblings and other children understand better what some go through....well, I am just amazed !!  Within 2 weeks of her release, she jumped to #3 on the publisher's best sellers list, was #1 on 'Amazon's Hot New Releases' in both of her categories, and was in the top 10 of Amazon's Best Seller's list in her categories.....I tell you this not because it has anything to do with me.....I tell you so that you can see how much of a need there is for hope against hip dysplasia !!  I am thrilled that HOPE is filling such a void, but I am heartbroken to realize how long that void has been there, and how many need her.
I have to say to my "partner in crime", Julie, that without her, Hope never would have happened !!! And, without our dear friend, Cherie Turner, HOPE wouldn't have come to life !!  She drew her perfectly and I fell in love with her face, immediately !!!! lol.....most importantly, God.  Without God and his grace, HOPE couldn't have been born.  God is the source of all hope.....and He, himself  wanted this book done.  It is His idea....his words...and He has brought her to fruition.  He touches people through her (HOPE), and I am just so privileged that he gave me the grace to not be consumed by that "poor me" feeling that I had....and that, He allowed me to play a small role in HOPE's being !!!! ;)

Here is the link, if you would like to purchase Hope, the hip hippo.....this link goes to our publisher's site, but please, please know (especially if you are international) that Hope is available on Amazon and Barnes & Noble !!!!

Hope the Hip Hippo

Aside from what is needed for marketing/advertising type blah, blah, blah.....all proceeds from the sale of HOPE go to the:

Purchasing HOPE directly benefits those with hip dysplasia by helping to fund further research and spread awareness !!!!!!!!!!! ;)

God bless you, each and all....you are always in our heart & prayers....and we are so grateful to you for choosing to be a miracle for our Mia !!!!!

With a Mommy's grateful and humbled heart,

xoxoxoxo

One Hip World

We are so happy and proud to be able to be a part of this event and in making a difference in the lives of these children and all those who suffer (and suffer, they do!!!)  with hip dysplasia !!!

One Hip World is a world wide day of fundraising to take place before, but preferably on
JUNE 30, 2012 !!
The idea is for YOU...WHEREVER you are in the world, to hold a fundraiser of your choosing, be it a bake sale, book sale, auction, bike ride, 5K walk/run, etc....and then take a picture of you and your 'team' with the check before you send it directly to:

The International Hip Dysplasia Institute
83 W. Columbia St.
Orlando, Florida 32806

Because the International Hip Dysplasia Institute is a Non-Profit 501 (c) 3, your donations are tax deductible, and 100% of the money raised goes towards furthering research and education on hip dysplasia !! ;)

We wish to thank Larry the Cable Guy and his Git-R-Done Foundation for their support of us in this world-wide endeavor to make a difference !!!!!

Git-R-Done Foundation 

Together, we can STAND FIRM as we band together to have HEALTHY HIPS 4 LIFE !!!!!

For more information, please email:  onehipworld@yahoo.com

One Hip World

or visit One Hip world on Facebook !! 

All proceeds go to the:

Always with my heart,

Mamma !! ;)

Enjoying the break...

Wow !! I can not believe it has been almost a month since I last blogged !!!! Shame on me !!! I'm so sorry !!!!  It's amazing how one day just sort of rolls into the next, and before you realize it, a month is gone !!  I also can't believe that Mia has been out of her cast for a month !!!  Truth of the matter is....we are really enjoying this break !!  Mentally, physically, spiritually, emotionally...you name it, we needed it !   Life without a cast is so much better !!! She is loving the freedom !! I wish I could make her understand that the more she uses it, the more it will hurt, but, she is 2 and what can ya do?  During the day, she is all over the place !!  We didn't expect her to crawl, walk or do much of anything for at least a year.  However, our girl (who continues to amaze me daily!) moved her legs as soon as the cast came off!  She insisted I put her pants on (didn't expect her to be able to close her legs enough for that), and when asked if she wanted to ride home laying down (her usual casted position) or ride sitting up, she said, "sitting up!!!".  And so she did.  4 hours out of the cast, she looked at Daddy and said, "I want to stand".  And, so she did.  The next day, she announced, "Mamma, I want to crawl"...and, so she did.  Her spirit, determination and 'can do' attitude just amaze me !! 

Standing up, testing out the new hip just hours after having the cast removed.  ;)



Her new favorite thing to do, is to hold your hands, so that you can help her walk.  I have no doubt that before long, she will be letting go, and doing it on her own.  She's already trying.  Only one thing stops her.  The pain.  Unfortunately, her nights are usually still pretty 'ugly'.  Using her legs so much during the day, brings on some horrible pain at night.  In turn, the pain will usually trigger a night terror or nightmare of some kind, and so our old routine continues.  I do, however, believe we are making progress !!  When she does have a good night, it's GREAT !! She sleeps straight through 10-12 hours or so.  We are going longer and longer between pain med doses...and overall, during the day she seems happier !!  Much happier !!  Now, if we can get the nights to get in line, all would be good !!
We are looking forward to holidays, particularly since we know we won't have to deal with casts or surgeries...and we'll even get to spend her birthday (in Feb.) without them as well !!! 
We see "the amazing" Dr. Heflin again on Jan. 23rd, to discuss the next surgery, which will be sometime at the beginning of March....but, you know what ??  We 're not going to think about that right now !!! We will cross that bridge when we have to, and for now....we are just going to continue to enjoy the break !!!!!

Here is a little video scrapbook I made of Surgery #1...I apologize for it's length...trying to get 3 1/2 mos. down to 8 minutes was tough !! haha...and I'm sorry that I couldn't include everything...we have been so amazingly showered with love throughout this ordeal, that I could not possibly include it all....but this will give you a pretty good idea of that love and of what we call "Team Mia" !! ;)

We love and appreciate each and everyone of you !!!!! We are blessed beyond words and beyond measure !!!!  And, we are so proud to call all of you our friends !!!

Thank you for all that you are, for all that you do...and, for just being you !!!!
And, thank you for being a miracle for our Mia !!!!
With a Mommy's heart,
xoxoxox

A "complete" song....

This week's lesson....in life, in order to have a "complete" song...you must have both 'high' notes, and 'low' notes.

All 'high notes', and you get a sound that can almost begin to hurt your ears.  You just can't sustain that for long.  You need to be able to settle back down.  All 'low notes', and the song gets dismal, dreary, and to me just stagnant.  You feel as if it "isn't going anywhere".  It just doesn't do much to lighten your spirit.  If you're really lucky, you get the beautiful sound in between the highs and lows...known as the 'melody'...the thing that carries you through.  I believe that the highs are meant to 'enhance'...the lows are meant to be your foundation, to learn from and build on.  And, the melody is really just the "whole point"!

Our 'highs' come in forms such as that amazing weekend with our Il Volo family, which, I just wrote about in the last post.  They also come from each of "Mia's Miracles", of which, you are one.
Our 'lows' come way too often in the form of pain and suffering for our Mia.

Nights like tonight are a low.  8 weeks out of surgery...8 weeks in this horrible body cast, and still her spasms and pain are unrelenting.  I sit for hours and rub her little leg.  I watch her as she wiggles and moans in pain.  "Are you ok, Mia ?"..."what can Mamma do?"...."just rub me" says her little voice.  "Just stay with me and rub me."  And, so I do.  Willingly.  Gladly.  Anything to ease her pain.  Anything to see her smile.  There were no smiles tonight, just pain and sadness.  As she lay there clutching her "Ignazio" pillow in one hand, and her "Goofy" doll in the other,  I watched as she began to relax and doze off, and, my heart ached.  Please don't misunderstand me here. We, as parents (and every parent I have spoken with whose child has hip dysplasia has said the same thing!) in the grand scheme of things, we are very, very VERY grateful.  We are wise enough to know our blessings.  When it comes to what is wrong with our children, we are grateful that it is, so called, "structural" and can be fixed !!!  And, we, I, thank God everyday for that !!!  The problem is that the 'uncertainty', the 'fear', the 'pain', the 'suffering'... they are all very, very real.  I want so badly to take this from my Mia and do this for her, I could die.  I would die. For her, absolutely. 
However, I can't....and right now, I, Daddy, and each of you have the amazing privilege of being her 'melody'.  The thing that carries her through.

One day, she will be strong enough to sing her own melody, and, while your 'part' may change, you will always have a role to play, and we will always be so grateful and blessed that each of you have chosen to be part of Mia's song.

When you aren't strong enough to be your own 'melody', I believe God gives you those you'll need to help carry you through.  I also believe that you always have that choice for others.  You can choose whether or not to be someone's melody, and carry them through.  You can choose the part you will play in their life.  A 'high', a 'low', or a 'melody'.  "Enhance" , make "dreary", or "carry them through"...always yours to decide. 
Each day, new songs....new opportunities.
The fact that you are here is no accident.  You chose to click on her link.  You chose to visit this blog.  By doing so, you chose to be part of her song.  And, your music warms our hearts.

I made this page to share Mia's journey with you.  Sometimes we celebrate.  Sometimes we cry. 
But, all of it, we do together !!!  In perfect harmony.

With a Mommy's "singing with gratefulness" heart,
xoxoxo

A true 'high note'....

A few posts ago, you read all about our Mia's great love, Il Volo !!  I talked of their amazing talent, their gentle hearts, and their kind and loving souls.  This past weekend (Oct.9, 2011), thanks to our dear friends Linda, Annamaria & EMI Vision we had the astonishing gift of being able to attend their concert in Melbourne, FL !!!
At every concert on their North American tour, Ignazio, Gianluca & Piero have dedicated the concert to Mia.  They have shown the most beautiful video of her, their "biggest fan", and the world watches as our girl sings and dances with "her boys".  The video was done about a month before her first surgery, and everytime I see her standing and dancing, it warms my heart.  I know we will get her back to that point one day, and it gives me hope!  After they play the video, Gianluca says, "and, now, Mia, you must be strong and get well."  Piero chimes in with "one day your wings will be strong enough and you will fly to us."  And, Ignazio, with his tender heart always looks so choked up, and begins the Elvis Presley song "I Can't Help Falling in Love with You"...a song they have no way of knowing has always been my favorite Elvis song.  And, so the three of them sing to her.
At the concert this past weekend, it was so nice to hear Ignazio say, "our Mia is here"...and Piero say, "finally your wings are strong enough, you fly to us".  They held her, they kissed her, and they took her heart on an incredible flight !!! Here, I'll let you watch.....

I know.  Simply amazing.

For a brief period, Mia completely forgot her pain.  She forgot her cast.  She forgot all of the ugliness that this whole ordeal has given her.  And, with every ounce of her being....she laughed, she clapped, she sang, and she danced.

You cannot imagine how much I have missed seeing her like this !!!!!

How do you begin to thank Il Volo for the way that they love her? 
How do you begin to show your appreciation for this gift ???
Ignazio, Gianluca & Piero are loved by us for many reasons, but the way they have taken her as their own, worried about her, prayed for her and loved her completely is quite simply, God himself.
These boys are Mia's heroes.  Particularly, her Ignazio.  I do not know if even they realize how, they give her hope.  She draws strength from their love, and they do something for her that I, Daddy and others couldn't at the time....through all of her pain, they made her smile.  I watch her as she watches them, and I am amazed.  Such, a tremendous love from such a little heart. 

Both Daddy and I are so grateful to Il Volo...to their families...to their managers...their production companies...to their fans, and, everyone associated with them !!! They immediately opened their arms, and welcomed us to their family !!!
We will carry you all in our hearts !! <3 <3 <3

A few pictures for you, so that you can share this moment with our Mia.

left:  Mia & Mommy before the concert.    right:  Daddy & Mia after.