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Messages for Rocco Baldelli

 In an interview with Scott Miller of CBS Sports.com, Rocco Baldelli, in talking about this web page said:

"I've seen it," Baldelli says of the site's tribute to him. "I was kind of shocked when I saw it. Somebody told me about it, and I didn't expect all of those messages. It didn't dawn on me what might be on there. It's very nice. A lot of people are pulling for me, and I do appreciate it. It shows a lot of people dealing with this that, hey, you're not alone."    Click here to read the entire interview. Send your ROOT FOR ROCCO message to root4rocco@umdf.org .
IT MAY TAKE 24 HOURS FOR YOUR MESSAGE TO APPEAR HERE.
 
 

Rocco,

Yes, yes...I'm a Red Sox fan.... However, I was so impressed with the Devil Rays. I was rooting for them during the World Series.

This past year I too have been diagnosed with mitochondrial myopothy.

My doctors haven't been very good with giving me advise about excercise. What do your doctors recommend?

Good luck and I wish you the best. You still have your whole life ahead of you. Just think of all the people you have touched in just 27 years.

Mary-Ellen Sokolowski

====
 
God Bless you.  We are just now getting all of our son's test back  its been 9 months waiting.  Ayden is 4 years old and through an MRI we just found out he also has Leigh's disease.  I havent been sleeping well the stress just keeps my mind running to try and find ways to find a cure and before I found out about you having this disease I was looking into different fundraising events one was to get our Cincinnati Reds next season maybe to have one of there games have a percentage go towards the www.umdf.org for research.  I already came up with a slogan help STRIKE OUT mito disease.  Theres a reason God gave me my two beautiful children my daughter she's 2 has down syndrome and my 4 year old is the one with mito  We will make a difference in this disease we have a huge support group through our family and friends with tons of ideas on raising awareness.
Nest spring we are having a bikers run funraiser this brings in alot of money.  well I better get off of here    God bless you and stay strong.  shelly faith and ayden

 ====

Rocco- From the bottom of my heart; Thank you.  My mom was diagnosed with mitochondrial myopathy two years ago. You have brought this disease to the forefront and remind people everyday of the struggles that those with MM experience everyday.  More importantly, you reminded my mom that people can LIVE with disease. She called me as soon as you hit your HR to ask if I saw it.  Thank you for hope on a dark day and for educating people on this disease so that they may do something about it.  My thoughts, prayers and thanks to you and yours. 

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Hi Rocco,
   You've been my favorite player ever since you were drafted by the Rays and I'm so glad you're in the World Series!  I was lucky enough to be at Game 2 and see you play all 9 innings.  What a great game!  I just wanted to tell you how impressed I am with the way you've handled yourself dealing with such a difficult illness.  You are truly a great guy and a real inspiration!  Good luck with everything.  Go Rays!!
 
Aimee Hawkins
Nashville, TN
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Dear Rocco, 

My niece is almost seven years old and we found out about her almost two years ago.  Her case is very different from your case, as in many mito patients.  She is losing her brain cells.  I remember when I first found out and trying to find people to talk to about her condition and I was unable to.  I was at Game 2 and I had tears in my eyes to see you play.  It gives me hope that my niece will once walk again and maybe speak.  She lost the ability to talk over 8 months ago.  This has been a hard couple years for my family but hearing how you are overcoming obstacles has put smiles on our faces. 

 Thanks and good luck,

 Michelle

====
DEAR ROCCO,
 
WAY TO GO ON YOUR HOME RUN!  I'M WISHING YOU THE BEST WITH YOUR HEALTH!  I AM THE MASCOT FOR THE ST. LOUIS CHAPTER OF UMDF.  MY NAME IS MIGHT MITO!   IN CASE YOUR WONDERING I'M A TURTLE.  I ENJOY BEEN THE MASCOT BECAUSE I CAN SEE ALL THE SMILES ON ALL THE KIDS FACES.  WE HAVE OUR FAMILY FUN DAY IN APRIL OF EVERY YEAR!  THIS YEAR IT WILL BE APRIL 11, 2008. IT'S SO MUCH FUN GETTING THOSE KISSES FROM JENNY, DANNY, SARAH, AND RONNI. IT SEEMS EVERY YEAR THERE IS ALWAYS SOMEONE NEW.  GOOD LUCK LOVE MIGHTY MITO AKA. DIANE
====
 
Hi Rocco,

I just wanted to tell you how proud of you I am. I am 22 and was finally diagnosed with Complex I and IV back in June after YEARS of looking to pin-point exactly what was going on with my body. I played softball, volleyball, and swam competitively up until the past 2 years. My teammates would always wonder why I would be sweating or exhausted after little work, and all I could tell them is that my body feels like it got hit by a truck, and I was just tired. While all this was going on, my brother was suffering completely different symptoms, but was diagnosed with Mito back in 2001. It took 7 years to figure out what is going on with me, and I think that other patients with Mito will tell you that it takes a lot of patience to cope. Although it may not be what you want, it is something concrete that now explains what is going on. I know that you want to handle it privately, but just know that I (and the rest of the Mito community) are here whenever you need us. You are a true diamond in the rough and have shown nothing but class while still being a professional athlete- I don't know how you do it! You are a true inspiration and please don't let the media or hype get to you- better said then done, I know. I (we) understand that you are a person too, and really hope that you get the peace and strength that you need to battle this disorder. You are an amazing athlete, and I am so proud of how you have handled yourself in the face of everything.

Much love,

Amy Burgener

====

Dear Rocco,
 
I recently heard about you and your story from my mother, who is very involved with UMDF. My younger sister lost her battle with MELAS at the age of 26 in 2001.
 
I think your courage and what you have accomplished is amazing.  I hope that you will continue to be a "spokesperson" for  mitochondrial disease.  I cannot say enough about this organization.  I truly believe that Chuck Mohan and other members of UMDF greatly prolonged my sister's life as well as bettered her quality of life and spirit.  They gave her hope, friendship, and support like no one else ever had.  It was hard being different, sick, and not really knowing what you are up against.  UMDF was Heidi's family, as well as our family.  The love and support we received from board members, staff, and other families dealing with this horrible illness was unlike anything I could have ever expected.  This group is unique and I hope you find the same comfort, support and hope that Heidi found here.
 
Best of luck to you.  Thank you for being a face and voice for mitochondrial disease.  As I can see from all of the letters you have received, you have many fans and supporters and you have become an inspiration to many!  My sister would have been so excited and proud to see you play.
 
Best Wishes to You!
-Tami Mee
(in Loving Memory of Heidi Marie Daniel)
====
Dear Rocco, Because you have an Italian last name I am wondering if this disorder might be related to the Mediterranean countries.  My whole family on my dad's side is just filled with pain and exhaustion, and several of us (me included) have cardiomyopathy and severe arthritis-like symtoms.  And we are always getting injured for no reason.  When I see you come up to the plate, I think, There is someone who knows what we are going thru.  And look at him go!!! 
Since this is a genetic disorder, I know in my cellular-disarray-filled heart that one way or another, with the help of stem cell research, we will find a cure for this and go on to a sweeter future.  This is why no one reading this should ever give up. 
 
Rocco, how hard it must be to be so young and have such a great career in front of you, then have an injury, approach it with mental and physical stamina, only to have the same thing happen over and over again.  You have to become wise beyond your years, which is one of the perks of illness.  Pace yourself, take good care, and know that many people are wishing the best for you.  God bless, Patty Capetola and family, originally from Philly, now living in St. Pete
 
====
Hey Rocco
Red Sox Nation wishes you the best.  Keep fighting.
 
====
Dear Rocco,

I recently became aware of your mito.  As a Mom with Mito and 2 sons
with mito,  I told them about your condition and that you are a
professional baseball player!  Since I live in the Philly area, I have
to root for the Phillies but honestly, I am so impressed with your
recovery that I'll be rooting for you when you play!

Sounds like what the mito community called a "crash" early this year.
I have had crashes as well as my sons.  Get the rest you need, take
your supplements (which I assume you are on!)  I had a crash 4 years
ago where I needed to use a walker.  After a few months, I was fine.

Thank you for coming forward with your diagnosis.  It's a disease that
most doctors don't even know about.  Keep up the great work and have a
good rest after the series is over.  When your body says "I can't do
it" listen to it and take the rest you need.

Your a hero for the mito community!  Thank you so much....

Carol DuPon
==== 
Hi Rocco,
 
We are young adults who have diagnosis of Mito too.  We are cheering you
on in the World Series games.  One of us is an unemployed artist in college and the other an
umemployed occupational therapist, presently in the hospitall not feeling very goooooood. 
 
How do you manage to run those bases? and withstand the length of each game?
What keeps your stamina going?  Do people run bases for you at times?
Our stamina is not obviously like yours.
 
However, we wish you the very best.  And we are
so glad that you, in your efforts, can help the cause for many of us with Mito by making
it publicly known across this nation.  Many even in the medical world do not know of it
and others do not understand its ramifications on the body's systems or its impact
on holding down a job. 
 
Many of us do not have insurance that covers all of the testing and medical
care that is so sorely needed or even daily care assistance to relieve caretakers.. 
 
Mito can be quite debilating and end a career and even a life due to complications.
So it is so wonderfulllllly great to know that  you  are  working on trying to keep your career.
We hope we can do so some day toooooo.
 
We are rooting for you Rocco!!!!!
Aly and Heather of Allentown, PA 
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Dear Rocco ,
I am 70 and when i look at you , i see DiMaggio--------- you were a stud in game 2 of the series------ Played like the true champion you are------------------ I am glad you are the fighter you are , you are only 26 , so there is still time to reach the 5 tool potential you came up with .
And i believe you will do it .
A Bronx Kid ,
Albert
====
 

 
Hey Rocco, Nice to see you in the World Series. My name is Darren and my 10 year old daughter was diagnosed with Mito in January 08 and it has been a long unpleasant road.I just go to bed each and every night and hope for the best. Got to be strong and keep my head up.Now I see a man in the world series with Mito and it helps to see you out there and playing cause Kaitlin likes to do cheerleading and I just cant tell her no so she pretty much gets to do whatever cause I feel like one of these days she wont be able to do that kind of stuff. Me or my family hasnt ever heard of Mito till this year and my wife has been in the medical feild for along time so that tells you it doesnt get talked about much.I read alot on here bout all the people that has this and makes you wonder how it has been kept a secret for so long.Well I want to Wish You the best of Luck out there in the world series and every thing else.Good Luck the Timmons Family.

====
 
 
Rocco:

 I'm sorry that you have to be suffering mitochondrial disease in order to get the disease known by most of the US and even the world as they watch you play baseball, but all eyes are on you now.  You are a celebrity struggling with a disease that is not well known by the world.  They are going to see how you handle it  and they are going to want to know more about what YOU have.  Now we will begin to get more recognition about mitochondrial disease.  However, as I too have mitochondrial disease, I struggle to get through my days.  I pray for you as you continue to live through every day -- and make each day a normal one!  Thank you for getting back into your chosen career and being an example for all of us!

 Joy E. Krumdiack

Washington State Ambassador

for UMDF

====
Hi Rocco,
 
I have been inspired by your story. I was so excited to see you play 9 innings in last nights World Series Game. You made an awesome double play and loved the effort at home plate!! I am 46 yrs old and recently diagnosed with a mitochondrial disorder. I appreciated the news coverage during the World Series talking about what a Mitochondrial disorder is when you were up to bat. I have been telling my family and friends to root for you and your team. Keeping Playing Rocco!!
 
God Bless,
Cathy in California
 
 =====
hi, Rocco,
 
We are baseball fans here! I just want to say thanks! for letting the world know you have mito. i have twins a boy and a girl both have mito My daughter has comnplex IV and my son has a undiagnosed mito. Not many people even know what mito is. with your telling the world now they know. I hope you have a good season and good luck to you and our family!! take care!
 
Kim Lawton
NY

 
Dear Rocco, what a great game! I am very proud of you. I am Brittany Wilkinson and I am the first youth ambassador for the United Mitochondrial Disease Foundation. I want you to know I am praying for you to continue to do well and keep your energy up. I sent you something in the mail so  keep an eye out for it. I just got out of the hospital after a month and am doing pretty good. I am proud you have raised awareness for mitochondrial disease but sorry you have it. My mom and my sister and brother have it too..
You truly are an inspiration to all of us who suffer from this devastating disease, and I am very proud of you and what you can do. I will continue to pray for you and together lets continue to raise awareness and find a cure. Our future depends on it. Keep on keeping on!
God bless,
Brittany and Freedom (my service dog)
====
 
Rocco,
I am just found out I have Mito and the age of 30 after looking for an answer for 5 years. When I look at you I know that I can still keep my dreams and make them come true. I was so upset about this disease before but I know now that I will be okay. Nothing will get us down! Good job!
 :-)
 
Holly

====

Hi Rocco,

I wanted to send you an email of encouragement and wish you the best of luck in the World Series, I know myself and all of my family and friends will definitely be rooting for you and the Tampa Bay Rays. Thank you for putting a face to something that many are so confused about, thank you for making me not feel ashamed of having this disease. I almost died last year because of mitochondrial disease and I was diagnosed at an older age (19), but when I got my diagnosis it explained almost every problem I have ever suffered in my life. I had no idea what this disease was when I was first diagnosed and had no idea what my future held for me, but now seeing your struggles and triumphs I know that I can do whatever I want to do, thank you for being my unsung hero, thank you for showing me that this disease does not define me and my life, thank you for showing me that there is hope. I want you to know how much of a hero you are to me and to wish you the best of luck with the world series and everything you do in life. Thank you for showing me that I have to power to change my nightmare to a dream.

 Wishing you well and the rays victory!

Leslie and The Whitt family

===

Hi Rocco,

 My name is Bobby and I am 9 years old and have mitochondrial disease too.  I think it is really cool that you play professional baseball.  I play tackle football for my town.  I know how hard it is to have to practice and play when you don’t feel good, but you have to keep trying really hard.  Don’t give up!  You have to work a lot harder than everyone else, but it is worth it.  When I am on the field and everyone is cheering for me, I kind of forget I have mitochondrial disease.  Now that I know there is someone like me who is a professional player, I think I could do that too someday.  Do great in the World Series; I will keep cheering for you!!!!!!! 

 GO ROCCO!!!!!!!

Bobby Arnold

 P.S.  Don’t forget to give your mom and dad “thumbs up” when you’re on the field, so they know you are ok and won’t worry about you.

==== 

Hi Rocco!

 Good Luck in the World Series!!  Know that there that there are parents of affected kids all over the U.S. rooting for YOU!  You are an inspiration and a source of hope for all of us.  We follow your struggle and find strength and hope that our kids will be able to accomplish all that you have.  Those of us who live with this disease every day, realize the enormous amount of human spirit it takes for you to walk onto that field to play.   

You are a hero to our kids, not because you can hit a ball, but because you are one of them.  Because you are affected with mitochondrial disease and you haven’t given up.  Because you have shown them how to live courageously with mitochondrial disease.  Because, you have shown them that this disease does not have to define who they are.  You are what they could be if they get to grow up.  

 Thank you for sharing your story.  Your courage in doing so has had an impact on more people than you will ever realize! May God continue to bless you with strength, courage, and health!

 Lisa Arnold

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thank you rocco

my sister and her son both died from mitochondrial disease
 
kym chana scholl
10-15-1957
02-03-2005
yaccov coby scholl
09-29-1993
08-1993
 
 
dotti

====

 Hi Rocco,
 
Go Rays and go Rocco!!  I have Mito too, and you are my Hero.  You have shown all of us with this disease  or any disability, that you can rise above any challenge and do your best.  Your positive attitude and not giving up are an inspiration to us all.  Here's to a Champion on and off the field!  Rays and Rocco all the way!!
 
God Bless,
Phyllis

====

Rocco,
 
We are always rooting for you, in regards to baseball & beyond !
You have played so well. It was thrilling to see you hit a homerun & come up with a base hit for the
game winning RBI in the post season. Keep up the great work.
Wishing you the best !
The Prachniak Family

====

Rocco – you are truly an inspiration and give hope to everyone who suffers with the effects of MM.  I can relate, as I was diagnosed with MM (adult onset, with many of the exact same symptoms you experience) after nearly 4 years of searching for an answer.  Thank you for being such a fine example - for never giving up on a dream, regardless of the challenges you may be facing.  Though this devastating disease grips many people in different ways, a positive attitude clearly has an impact on the quality of life one can expect after a diagnosis of MM.

 Go Rays!!

 Kevin - Atlanta GA
====
Congrats on being a major player in the fantastic journey to the World series. We are original Rhode Islanders and now live in the Tampa Bay area. We have followed your career and have been praying for you and that you could get back to playing. Praying for a diagnosis and your return to the sport that you play so well. Now we are thanking God and praying for you to continue this journey of healing and we also pray for all those who are dealing with this disease.You have brought awareness to many ,so, good comes from difficult days. We will be watching you take the series and cheering you on.   Bob and Jane Auger
 
====

Dear Rocco,

That was an incredible hit that you hit against John Lester on Sunday.  My dad gave me the article on you that was published in the New York Times and The Dallas Morning News.  He is on the Board of Directors for the UMDF.  I hope to meet you someday. Congratulations on making the World Series.  I am rooting for your team to win.

Kelsey W. from Texas

====

 My 6 year old grandaughter has mitochondrial disease complexes 1 & 3.

She is in cheerleading, and taking piano lessons.  She is a ball of fire, and also loves to dance!!!!
I'm sooo inspired because of both of you!!!!
I have incurable cancer, but am considering going back to teaching.  Apparently all 3 of us have the correct state of mind, and I've learned this makes all the difference, since we are all doing quite well!!!
GO ROCCO  GO!!!!!!!!!!!!
Love Ya!!
Becky (2nd gen. Sooner)
Norman, OK
====
 

Rocco,
Thank you for your voyage into becoming the poster boy for Mito.  You didn't choose it, but you gracefully took it on.  Our son, Bryson is nine, has a rare mitochondrial disease and plays baseball.  Our family is part of the Mitochondrial Research Guild out of Children's Hospital in Seattle, though we live in Idaho.  Baseball (even Mariner's baseball) has been a comfort to us as we have watched our son struggle to hold on to life, or just struggle to run the bases.  Probably no one else would cry when they hear "Take Me Out to the Ball Game," but it sustained us when we knew the game was our reprieve from the hospital (I don't care if I never go back).  So know that your ordeal, courage and love for the game are shared by people dealing with mito all over the country--even Idaho.  We're wishing you the best.  Thanks again for taking on the publicity for mito.
The Potter family
====

 
Dear Rocco,
 
I am 31 year old and have a mito disease (specifically NARP).  Wow to actually have someone out there that people recognize is great.  It's been a long time coming to get the mito message outof trying to raise awareness.  Thanks for sharing your story.  Hopefully things will go well for you. 
 
Congrats on making it to the World Series.  Go ROCCO!!
 
 
Iwould love to hear from you after the World Series and hear how you are doing.
 
thanks
matthew
====

We have twin 10 year old sons, Christopher and Michael, with a mitochondrial disorder.  Thank you for going public with your diagnosis and helping people to better understand the disease.  For my boys, it has helped take the stigma away from it, knowing that you are a famous baseball player who openly talks about what you go through.  Best of luck – we’ll be rooting for you!

The Links

Palm Beach Gardens, FL

==
 
Everyone in the mitochondrial world is rooting for you.  Facing your disease and not letting it stop you makes you a winner already far and above the World Series.  We are all rooting for you, however, to add winning the World Series to your credentials.  Go For It!!! Norma Gibson, mother of Heidi Marie Daniel, MELAS.
====
 
 
Dear Rocco,
 
I wish you the very best and good luck in the World Series!  I am a die hard Cub Fan but they just can't get over the Curse.  I'll be rooting for the Rays to win the World Series.  My 15 yr old daughter has a mito disease but at the present time she is staying stable.  It's not fun watching this horrible disease take away your child's life.  You are a true inspiration for all those who suffer from mito.  Thanks for getting the word out.  I hope you and your teammates can help raise awareness and help us find a Cure.
 
Pat Charleston
Chicago, Il
====

Dear Rocco,

My name is Lori, I'm so sorry to hear about you diagnosis of Mitochondrial disease, I can sympathize with you, I get terrible pain all over sometimes it's so bad I can't sleep, or function, walking is even difficult,I was diagnosed in 2005 with mitocondrial disease comp It is scary, one time I was in the Ocean, on my way out when my legs tuned to rubber, and I couldn't walk, so I can imagine how scared you were, My first symptoms were big time Pain, and digestive problems, muscle weakness, even in my lungs, I get short of breath, doing the simplest of things

and I used to consider myself very athletic.I even played baseball.

So as you can see I know what you are and have gone through. The only benefit if there is one is that you are well known. You, are in a position with first hand knowledge of the disease, To bring awareness to this cruel hidden and unknown disease.If it were not for the likes of Michael J. Fox (Parkinson) and Lou Gehrig those diseases would probably not have received the recognition they should. It seems the only way to create awareness is if someone of stature has the disease and becomes the face of that disease. You would be such a great face and spokesman to help create awareness for Mitochondrial disease. Somehow we must get the word out It takes a famous face to raise the money for research..

 I hope you take it all.

Sincerely,

Lori Jubinville

May God watch over you and keep you healthy. :-) Keep smiling.

====

Rocco,
Being a former college baseball player, your story has grabbed my attention.  Being a mitochondrial myopathy patient and physician, I know first hand the incredible inner strength you have shown in your return to play, in any capacity.  I have never given a thought to the Rays, but you have changed that.  I am now a major Rays fan (actually a Rocco fan).  I suspect you have added tremendously to the determination it has taken for the team to turnaround.  You are living the dream, in more ways than one.  Thank you for your determination, your faith, hope and guts.  Show em how it's done the Mito way, bring some energy to the world series.
We're pulling for you,
Art Caylor
====

Dear Rocco; Thank you for coming forward about having Mitocondrial Disease I have a 4 year old daughter who has Mitocondrial Disease complex 3 and 4 as well as Retts Syndrome and she has a stuggle everyday of her life. I wish we in the United States could have some Federal funding to help find a cure for this awful disease. My daughter currently has 15 Doctors she will see on a regular basis for all her needs.  Thank you again Rocco maybe between all of us we can the word out about this awful disease. Sincerly, Lisa Ferguson Westerlo New York

 ===

We've been a Rays fan since day one.  Original season ticket holder and haven't stopped believing.  We lost a grandson to complications from a mitochondrial disorder nearly four years ago.  It took months and months before a disorder of the mitochodria was the diagnosis for young Collin Parker.  Unfortunately, at 10 months of age, he was unable to continue the fight.  Since 2004, we have relied upon the UMDF to provide information to help us understand the debilitating nature of diseases of the mitochondria.
We have watched you since 2003,  your advances on the field and the concern regarding your unidentified medical condition, the questions of diagnosis, etc. off the field.  Stay strong, continue to persevere and never give up- on the diamond or daily in your fight!! 
Onward to the World Series!!!!!!
Go Rays!!!! 
The David Family
Tampa, FL

====

Rocco,

Thank you for displaying the strength and determination publically to live “well” with Mito and still be a champion!

I have two sons 9 and 7, both with mitochondrial disease. Bryce is relatively high functioning but my youngest, Layke, is non-verbal and has huge cognitive challenges and a seizure disorder.  The awesome news is that he started walking 2 ½ years ago and began playing baseball with the Miracle League last year!  He loves it so much!  You are an inspiration to us all.  Keep winning and keep on being a winner – Show ‘em you can have a disease and not let it have you!!!!

 Marie Reynolds

Life is a joy!

 ====

 
Rocco,
 
Thank you, for going public.  My son is five years old and has Complex 1 Mito.  I wish you the best. I watch by son live with this disease and it breaks my heart.  He loves playing sports and just finish his first year of t-ball.  God Bless you and best wishes!!
 
Gina and Family
Wichita, Kansas
====

Hello Rocco,

My 11 year old son and I are huge baseball fans, my son Lenny was diagnosed early in life with Mitochondrial Disease (Complex 2). Lenny is unfortunately in Children's Hospital in Boston currently having another surgery, however we did watch you play Monday night on TV - You had a GREAT Game (unfortunately for us Red Sox Fans).

We hope you enjoy playing at Fenway Park - it truly is an amazing ball park, so rich in tradition and history. Lenny and I try and get to Fenway at least once per year and he too recognizes the magic of Fenway. When we go we have to get there early to watch all the pre-game batting practices and other pre game happenings and than we can not leave until the last pitch is thrown (No Matter what).

You are an inspiration to us. Just as you appear to be doing Lenny too tries to live his life to the fullest.

We wish you the best of luck on and off the field!

THANK YOU!

Lenny Gratton and Dad

====

Dear Rocco,

I have L.H.O.N. however that doesn't stop me.  I am a huge Baseball fan.  That was an incredible home run you hit yesterday.  I am so glad that the United Mitochondrial Disease Foundation is finally getting some recognition, it is way overdue.  I am rooting for you, so keep hitting those homers!!  I really hope that your team makes it to the World Series.

 

Best Wishes,

Kelsey W. from Texas

====

 

Rocco,

I am the mother of a 13 year old boy who is about to have a muscle biopsy , and is  looking at a mito disease diagnosis. I am a Bostonian and love the Red Sox, however when I heard your story,.. I could not help but rejoice for you and the Rays. You are an inspiration to our family. Thank You Rocco!!

Rachel Wise

 ====

Rocco,

 We would like to wish you luck in the ALCS and beyond! Our two year old daughter has a Mito disease, and we know what a struggle it must be, not only to deal with physically, but the wait for a diagnosis and how to treat it. We watched you blast a three run home run last night in game three, and couldn't be more proud! (Not to mention we are huge Yankee fans, so any damage to the Red Sox is a bonus!) Good luck to you and the Rays!

 Proudly,

 Chris, Alisa, & Morgan Rawski

====

I witnessed your 3-run homer last night and learned that you had mito, as I do.  What an inspiration!  God Bless and Good Luck!

Lori Fore

====

Dear Rocco,

I am a nine year old boy with Mito.  I also like to play baseball.  Great homerun in the playoffs,  I am cheering for you at home.  How are you feeling?  I hope the doctors kick mito's butt and find a cure.  Stay well!

 ====

WOW!!! Rocco hit a three run homer. You’re giving hope to the Mito community. We are all very proud in Orlando. Go Rays and Rocco!!!

 The Slauter Family

 ====

Dear Rocco,

May God bless you. Your family, fans, and your teammates love you and are praying for your well being. I pray that a cure will be found.

Love,

The Reinhart Families

Odessa, FL

====

Rocco,

You are an inspiration to all of us battling mitochondrial disease.  Keep on keepin’on!!!  You have made an amazing comeback – we are so proud of you.  We’ll be watching the TAMPA BAY RAYS as they make it to the World Series!!

 Pam Johnson,

Kansas City

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Rocco:

 I just read an article in our local paper about your rare disease.  It is not so rare.  There are many people dealing with this on a daily basis.  Especially children.  I'm dealing with it now with my daughter who is 10 years old.  You are sending a positive message to all here that you can still do things even when you feel you can't go on.  Your positive outlook is wonderful.I love baseball and will cheer your team on.  Good luck and go Rocco go.

Lisa Nerenhausen

mom to Leah

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 Congratulations to Rocco and the Rays...

We are so proud of you for spreading the news about Mitochondrial Disease. We are looking forward to a Phillies Vs. Rays world series!!!

Laurel and Dave Smith  (aka, Jamie's Mom and Dad)

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 Rocco - you are truly an inspiration. Our son, Jack, has mitochondria but doesn't let that slow him down. He is playing his fifth season of baseball and today his team won the game of the season!  Jack adores baseball!  There are times when he wishes he could run faster but his team ALWAYS counts on him for the RBI...and he never lets them down!  We will continue to ROOT FOR ROCCO!  And besides, us Italians have to stick together...GO ROCCO!!!  Bob, Susan, Gabby and Jack Milani

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We've been watching Rocco for his whole entire career and we are as happy as ever for Rocco to be playing again! And he fianally gets his chance in the postseason [hopefully the World Series]!

 The Brantley’s

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 We hear that you may be in the lineup for game 3 on Monday night!!!  Way to go!!  My son Jack who is 9 was diagnosed with a mitochondrial disorder last year and is inspired by your story.  Jack is a soccer player and a determined young man on and off the field.  Thanks for helping him, and others who face the challenges of mitochondrial disorders, see what determination (and exercise) can do!

 We live in California now but are originally from Boston so its hard not to root for the Red Sox, but you can be sure that we will be rooting for you too - loud enough for you to hear us all the way from California when you take the field on Monday night! 

 GO ROCCO!!!

 Stay well.

 Jana, Jack and McKenna Stoudemire

Del Mar, California

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 Rocco-

All the best to you in the playoffs... We wish you good health for a long time.

To him who is determined it remains only to act. Italian Proverb

 God Speed-

Marie and The Three Wiseguys!

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We are Rays fans in the Tampa Bay area -- and we have loved Rocco for his entire career here. One time, we were flying through the Pittsburgh airport, and a guy ran from way across the other side of the terminal when he saw my son's Baldelli jersey -- he said he was from Rhode Island and thought the world of Rocco, and wanted to hear from us how he's doing.

You were a marvelous ball player before -- you're truly an inspiration to everyone now -- this team is very special -- so glad you're a part of it!

We're rooting for you from Section 124 -- as a person and as a player -- Big hugs to Rocco Baldelli!

 

Claire, Tom & Carter Brantley

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DEAR ROCCO ,

 MY HUSBAND CHUCK AND I HAVE ALWAYS ROOTED  FOR THE BOSTON RED SOX .OUR DAUGHTER SHARON HAS MITOCHONDRIAL DISEASE . .THIS TIME WE ARE ROOTING FOR YOU TO WIN YOUR TEAM TO VICTORY . OUR BEST WISHES TO YOU . TERESITA L AND CHUCK A MCGINLEY FROM TUCSON AZ .

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Dear Rocco,

 My husband and I met you as a "Rookie" for the Devil Rays. We have always enjoyed watching you play. We were concerned about you for the past few years as one thing physical went wrong with your body after another. Thru all of your trials you were always upbeat and pleasant with what you were asked to do for the Rays.

Now you have a reason for your physical problems and yet you have come back to play for your same team, now THE RAYS. I hope you are having as much fun as we are watching you guys continue to WIN. GO RAYS AND ROCCO!

 

Colin and Marie Povey

Clearwater, FL

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 Congratulations and keep on going Rocco.  Do you ever make appearances to encourage the younger children who have MITO?  I have a granddaughter in Atlanta, who has had mito since she was 18 months old.  She is 3 1/2 now and we have almost lost her twice.  She is currently in the Scottish Rite HOspital in Atlanta Georgia ..she was intensive care for 2 weeks.  She had 100 seizures in a week.  Her mother and father are amazing.  Her mother last year organzied the first family fun day and mito walk in Norcross Georgia.  She will be having it again in March....the last week.   Do you think there is a chance you might be able to come to this to give some of these older children who come inspiration.  Pluse you would draw more crowds for us (although we had 500 people last year....it was a beautiful thing.).  It would mean so much to the children.  and to the parents.  If you think you might be interested please contact me at ssshalom@aol.com.  We fight the fight every day for my granddaughter ..Ainsley Paige...before she went into the hospital she could walk and chase the dog around.  Now she is in inpatient rehab at Scottish Rite learning to just even crawl.  She is a miracle child as twice doctors thought she would not make it.  Please find it in yourself to give of your time..... And you keep going....what an inspiration you are to all!   Sharon Simon, grandmother to Ainsley

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Hi Rocco….you have been my favorite Rays player since I have followed the team.  I am an Italian from Ct. and you are an Italian from R.I.  My mother was born in R.I.  I admire your spirit and you constantly giving 150% every time you are on the field.  Keep up the good fight…..it’s impossible to keep a good Italian down!  Judy

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 god's blessings on you, Rocco.   to know what is possible physically is best exemplified in your  spirit to "fight-despite."   those of us in the far outfield now have someone who can put our disease (i also have mito myopathy/deletion syndrome with PEO) on the map. thank you  for  letting the public know of  your illness.  i am a 56yo female(also Italian!) who struggles to get thru one 8hr shift/wk.  my husband and i  will be following  you and your team.

our warmest fond wishes to you,

cyndie & dan corey  Pgh,Pa

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I'm rooting for you!  I know a little 8 year old girl with Mitochondrial Disease.

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 I'm normally a big Marlins fan, but now I'll be cheering for Rocco and the Rays!
Keep fighting!
Josie London

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Your strength in the face of adversity and willingness to fight on are
an inspiration to me and make me feel grateful for my own health and
that of my family in a more immediate way.  You are an inspiration and
we're all proud of you!
Prayers, Love, good vibes and all to you,
Amanda

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Good Luck Rocco We are pulling for you.

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i wish you all the luck of the world, not only for your sportlife but
especially for your health and happiness.
helene degen

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Dear Rocco,

My name is Kaelei and I have mitochondrial disease too. I am ten years old. Thank you for sharing your story with us. You are brave. Play ball good and most of all have fun and be happy. I hope you win!

Love, Kaelei Kennedy

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Rocco,

 As one that deals daily with this disease while working and raising a family, I salute you and your efforts to get back on the field. You are an inspiration to us that know what it truly means when “your muscles just don’t work”. Keep on working hard and doing what you love. Go D-Rays!

 Dan S.

Union, Ky.

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 And good health

Steve Daley

Arlington, Va.

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I wish you the very best…and sincerely hope you and your teammates get to the World Series.  And this is from a die-hard Yankee fan! 

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 Dear Rocco,

 As a proud Rhode Islander and New York Yankee fan, I am rooting for you twice as hard (tee hee hee).   Also, my nephew was a member of the Hendricken High School baseball team and graduated in 2006.  :)  

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 Good luck and stay healthy.

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GO ROCCO!!!

 Rosanne Haroian

Alexandria, VA  (formerly, Providence, RI)

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Rocco, you are a true inspiration for all people struggling with a debilitating illness.  Thank you for your courage and spirit!  Cheers to you!  Jennifer

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Dear Rocco,

I'm  an adult battling a rare form of mitochondrial
disorder (possibly kicked into gear by having contracted Lyme Disease a few years ago).  I can't begin to tell you how much your inspiring story has touched my heart and given me renewed hope. I first heard about your health challenges while watching  a broadcast of a
Rays-Orioles game the night you got hit a key hit causing the Rays to win the game. After the announcer mentioned that you were battling a mitochondrial disorder it really got my attention and I was totally awed to see you hanging in there and still playing....and playing well!

Thank you for going pubic with your health challenges. Your public persona has given those of us in the mito community a "face". I have found that now, because you are so high profile and DID go public,more people seem to have heard of  mitochondrial Disease  and even understand a little bit about what it means to have it,  especially the
challenges faced by ADULTS with mitochondrial disorders.

Your heart has always been visible in the way you've lived your public life and the awesome way you've played baseball,  but now your courage, perservance,  AND  your heart are visible in an even more awe-inspiring
way.  Thank you for giving us hope.

You are in my thoughts and prayers in hopes that you will be given the health, courage, and strength to continue to  pursue your dreams.

You can bet we will be rooting for both YOU and the Rays.

Anita Brandon
Wrightsville PA

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Dear Rocco,

 Thank you for bringing a little bit of sunshine to all of us dealing with MITO.

 Donna

(Mom to 17yr old just diagnosised)

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I have a 19 year old granddaughter who has had this disease for years, in and out of the hospital with many fears, but so far with the help of God she has over come and is still smiling.  God bless you and all who have this horrid disease and all who are taking part to find a cure.
Grandma Angie

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 ROCCO       GO RAYS…..   WHAT AN INSPIRATION YOU ARE to those who are sick and suffering with Mitochondrial Disease

My family, friends and my thoughts and prayers are with you.  Good Luck Hit Em Hard.

Cathy Anderson

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Dear Rocco,

 I am Ben the 12 year old son of Matt and Cindy Cruz well when my mom said I usually get a pinch runner, that is not true I sometimes do.  Also I am not the fastest runner but I am about average.  I will be routing for you in the playoffs against the red sox, it will be a tuff game but if you play well I think you will win the series.  So have a good game.

Go RAYS

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 I’m a Red Sox fan, but GO ROCCO!!! 

 Adam Burns

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I will be following you and wishing for the best.  My 17 year old son has mito disease (Complex 2) and is deaf.  He is very bright and doing so well in spite of all the limitations.  Please continue to help get the word out there about this awful disease so we can eventually find a cure.

 Marsha Smith

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I wish I'd have known before you eliminated the White Sox.

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Crush 'em Rocco!!!

We're rooting for you.

 Ron Hahamy

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 You are an inspiration to many and have done an important thing in bringing greater awareness of mitochondrial disease to the public.

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Have a great playoff run.

J.P. Szambelan

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 That is wonderful that you are able to return to what you love.

Best of Luck,

Juju Bug

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 GO ROCCO!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

Lauren

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You make it real, Rocco.  Go Rays!!!

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 We are die-hard Red Sox fans, transplants from the Boston area four years ago.  That was about the time my son started getting sick.  He was finally diagnosed six months ago with a Complex 1 Deficiency, a form of mitochondrial disease.  While we could never cheer for the Rays, we will be rooting for Rocco!  We appreciate your persistence in the face of this mystery illness, and your patience in trying to explain it to others.  We hope you have the series you've always dreamed about!  Best wishes, and thank you for never giving up!

 The McFetters family- Butch, Kristin, Kyle, Brendan and Zachary

Columbia, MO

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Wishing you continued strength to continue your fight with Mito. You are an inspiration to so many!

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GO ROCCO!

 Jen 

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God Bless you Rocco as you as you lead the Tampa Bay Devil Rays into the American League Championship!  All of us in the Middle Tennessee Mito Group and around the nation are so encouraged and inspired by your performance.

ROCK THE HOUSE ROCCO!

Fred & Paula Durham

Nashville, Tennessee

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Keep up the hard work Rocco.  I live in St. Petersburg Florida and I have been diagnosed with Mitochondrial Myopathy as well.  You give us all hope in your health and in your career.  Stay strong and healthily.
 

Best Regards,

Sherri

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 As a mother of a child with a Mito disease I want to thank you for getting awareness out there for people with Mitochondrial disorders.  Sending lots of support and good wishes your way! Here's to hoping they find a curefor mitochondrial disease soon!

 
Thanks
J Holleran

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I am a proud Rhode Islander and a proud Red Sox fan – but I am rooting for Rocco Baldelli.

He is an inspiration to all those suffering from mitochondrial disease.

I wish him continued success and hope. Stay healthy Rocco and keep fighting!!!!!

 

Dawn B.

Arlington, VA

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There is so much out there that people are not aware of.  Gods Blessings for you for contiuned health and success.

Way to go Rocco!!!!!

 Jennifer S. Porter

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I just want to say you go Rocco. I am a member of the UMDF for various reasons but the most important one was my son Tylor who passed away 6 years ago at 6 1/2 years old from his mito disease and I want to find a cure!!

 Rocco, you're an inspiration and I want the Tampa Bay Rays to win win win!!

 Sincerely, 

Alisen Gross

(mom to her mito angel Tylor Ryan) 

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Rocco,

My son is a 18 year old sports geek who just happens to have mild mitochondrial myopathy.  He would get frustrated explaining his disease  to people so he would just call his disease cerebral palsy because people knew what that was.

Now, you have given this mystery disease a face and name recognition.  He's proud to say he has mitochondrial myopathy just like Rocco of the Rays!

Rock on Rocco!  For John!

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Rocco:

 I am the father of two boys, ages 17 and 12, who both suffer from Mitochondrial disease.  My youngest, Ben, is an avid baseball fan and player, so we will be following your progress throughout the playoffs with great interest. 

 My wife and I, along with a few other families in the area has started a fund raising effort for the benefit of Dr. Saneto and Children’s Hospital here in Seattle.  We are mid-stream in the process of developing a Center of Excellence here in the Northwest.  So far, in just six years, we have raised approximately $1.0M for the study, diagnosis and treatment of Mitochondrial disease.

 Even though we are entrenched Mariner fans, we will be pulling for you and the Rays this year.  You did not choose this mito path, but now that you are on it, please know that you have our support and best wishes in all that you do.

 Go Rays!

 Best Wishes, The Cruz Family.

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Will be rooting for you while we watch the games. Our 2 year old granddaughter has a mitochondrial  disorder.

McKenna’s grandparents

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I vote for Rocco

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Thanks

Jo Bozek

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Dear Mr. Baldelli,

 We want you to know that we think it is awesome that despite the diagnosis of mito disease you are playing against the Red Socks in this very important game!!  Our family sends our best to you now and always ~ we know mito – both our kids are suspected of having pretty much the spectrum you have and we know what emotional and physical toll it can take on a person and a family.

 Though we are 1/3 Red Sox fans, 1/3 White Sox and 1/3 Mariners fans (well we live in Seattle) we can easily bring another team into our favorites to support you.  So consider us now Tampa Bay fans as well.

 Sean our 14 year old son played Little League for 2 years and became a rabid baseball fan and statistician.  Sports are hard for him as well.  Mito affects Sean in the fact that his muscles fatigue quicker too but most of all he has sleep apnea which makes it tough to get a good restful night of rejuvenating sleep to refresh the whole body and mind.  He still loves to play a friendly game of baseball and enjoyed a PawSox game this summer in Rhode Island.

 Our daughter (11.5 years) is particularly hit with the fatigue, muscle cramping and weakness.  Not great for a ball player or a ballerina such as herself.  Her dream is to dance in pointe shoes one day – to have the strength and endurance to achieve such a goal.  Like yourself she must balance out her energy stores and make choices on how to spend those energy allotments.  Your story has given her encouragement that with taking care of herself and balancing her life there is a future for her in dance.

 Thank you for sharing your story – thank you for being so many kids hero that deal with this disease.

 But most of all ------- Go Tampa Bay and beat the Red Socks!!!!!!!!!!

 All our best,

 The Denson Family

Kara (11) Sean (14) Alan and Marilyn

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Never give up, never stop fighting.
US 2008 paralympic swimmer
Joe Wise

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Hi There

 Grace can throw a ball about 5 feet and she can catch with the help of a Velcro mitt.  We will be cheering you on all the way.Good Luck Rocco.

 Shawn, Dori and Grace (Grace - age 5 has mito disease)

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 AS A RED SOX FAN, I WISH YOU PERSONALLY A GOOD SERIES, BUT I HAVE  TO ROOT FOR MY TEAM.

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Good going! 

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With two grandsons stricken with this, we know what you, Rocco, are going through!  We admire your courage and perservance!!  You set a great example for others!

 God bless and strengthen you, and give you grace, courage and wisdom!!!

 ----Grandparents in Clifton Forge VA

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What a great story for the ALCS.  Yea Rocco!  You are truly an inspiration.

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Yay Rocco we are so proud of you! You can do it!

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