Saturday, October 30, 2010

A Thousand Smiles

A post from Pops:

Last Sunday we attended Mass at a small neighborhood church in Cornwall, N.Y.  As providence would have it, the Gospel reading included this passage from St. Paul:

            I have competed well
            I have finished the race
            I have kept the faith

While Paul’s entire message speaks of the great difficulty of maintaining an enduring faith, the same progression of spirit is certainly needed to endure an illness.  And what is the reward for such dedication of purpose?  For us, the prize has been the greatest of blessings: Kelly’s apparent return to good health.  And so we continue to pray with increased confidence for others, like young Peter Marotta and beautiful Nikki Meyer and their families, that they too will experience the joy of God’s grace and a return to good health.

Friday, October 29, 2010

"Living It, Loving It, Sunday Riding"

Check out this great video filmed by Kelly's friend Blake a couple of years ago in Jax! The whole family was laughing this morning, watching Kelly enjoying a good ol' time...especially at the end!

http://www.youtube.com/watch?v=48mipLpzZmk

Thursday, October 28, 2010

Up, Up and Away!

Tonight's update from Mom:


   Since early this morning family and friends have been flowing in and out of Kelly’s hospital room bringing laughter, good cheer, flowers (including the strangest BRAIN flowers from France) and yummy goodies (Magnolia Bakery cupcakes and chocolate-dipped cherries!)  It has been quite an eventful day.
   Now that the storm has passed, we have time to reflect on one of our biggest blessings: finding the best neurovascular surgeon in the world to perform Kelly’s operation, Dr. Philip Stieg. His hands were guided by God.  How can we ever thank him for bringing Kelly through this delicate operation with such success? We will remember him forever!  If any of you ever needs a neurovascular surgeon, he’s the man!
   Kelly had her post-op MRI early this morning before we arrived.  Dr. Stieg reported this afternoon that the MRI came out fine (we will submit MRI and biopsy results to a few recommended oncologists for second opinions). He also announced that all her vital signs are normal and the leakage from the brain has diminished considerably, allowing him to approve her discharge tomorrow!  Yahoooooooooooo........
   After Dr. Stieg left, a skillful medical practitioner removed her head bandages and drain tube (Ani’s got it all on a video)!  We were so surprised at how little of her hair had been shaved and how clean and neat the cut was stapled.  It literally looks like she has a thin headband on her head.  It’s just incredible how the body adjusts to a major surgery and begins to mend so quickly when it is in the hands of experts.  
   So, the plan is that the Dillon’s will head back to Mountainville tomorrow and the wonderful hospitality of Tio Kurt, Tia Bea and our young cousins, Charlotte and Ernesto.  On November 9, Kelly returns to Dr. Stieg’s office to have the staples removed.  On November 10, 2010 we fly home to Panama!  Next week we receive critical info from pathology to determine whether or not she will need radiation. If necessary, our return date to Panama may change.
   If you ask Kelly, the highlight of today (aside from the meals prepared by her personal chef) was being able to wash her hair!!!!  The little pleasures of life!

~Mari

NYC Snapshots



"Hi Everyone...feelin' alright (like my favorite song by Rebelution says)!"
~Kelly
 
"Me and my man yesterday in the ICU :) He keeps a permanent smile on my face every second of the day!" 
~Kelly


La Familia :) Yesterday in the ICU
Pops hanging out this morning in the lobby down the hall from Kelly's room.
Check out that amazing print on the wall behind where Pops was sitting!
One of the many views she has from the 14th floor...
Thomson and I on our way this morning to deliver Kelly some flowers from the Fabrega twins and BethAnn.


**I am sorry for the "grainy" photos; they were taken with Blackberrys, which have very low resolution. I will try to upload better ones this coming week!** 

Wednesday, October 27, 2010

Update from The City That Never Sleeps

A letter from mom and dad...

Hello Family, Friends and Well-Wishers:
It’s Wednesday, the day after Kelly’s brain operation, and what a wonderful day it has been! 
Kelly walked the hallway of the ICU this morning and went up and down a flight of stairs. The two nurses that monitor the ICU patients’ motor skills were in awe of her energy and determination.  They told her that they will not be coming around any more to check on her because they say that after the hike she took today, her motor skills appear to be perfectly fine!  (CHEERS and LOUD whistling, banners and flags waving!!! Yahooo...  Way to go, Kelly!)
Kelly enjoyed her spectacular view from ICU.  She overlooked the East River and the Queensboro Bridge and on to Lower Manhattan.  In her quiet alone moments (which were very few!), she watched all the activity and the beautiful sailboats as they gallantly sailed by on the river.  She has also been pampered by all the hospital staff.  Their care giving has been unique, warm, helpful and friendly.  
One day Kelly will tell you about all her funny stories and hospital experiences (e.g., this morning a team of 6 residents tested her mental and physical abilities.  They began by asking her questions about POLITICS.  Those of you that know Kelly, know that politics is of zero interest to her.  After the second question, she quickly told them that she did not like politics and it was best not to measure her abilities in that curricula area!...and the story goes on...).  She has the gift of seeing things with a big humorous twist and her interpretation of life is fun to listen to!  She doesn’t miss a beat about her surroundings and if they keep her here long enough, she will have all the quirks in her hospital world identified with recommendations on how to fix the problems....she’s doing this within hours of having a brain operation!  That’s our Kelly!
I don’t know how Kelly and Ani swung it, but early this evening they moved Kelly to the “penthouse” recovery room.  We had been waiting all day for a private room to come available.  I think her brain started churning in this direction round 2 p.m. because she told family and friends to please leave her alone because she wanted to rest.  No sooner we got across the street to our hotel room, she started to send text messages saying we needed to do something quick about getting her a private room because the hospital needed her room in ICU for new emergency cases that had been admitted.  Mark and I were too exhausted and fell asleep, too tired and worn to deal with a problem that was not ours but the hospital’s.  Two hours later when we awoke, we found out that she and Ani had been busy spinning their magic web on the hospital offices.  
Since there were no private rooms available, the hospital put Kelly in their $1,600/night luxury recovery room at no additional charge!  Now, what are the chances!  The room has ceiling-to-floor windows overlooking the River and a fabulous view of the whole NYC skyline!  You know Kelly; she is twinkling with delight!  Tonight she had a meal prepared by the personal chef of the penthouse suites and she took full advantage!  Ani will tell you about those details!   
We may leave the impression that all this has been fun and games, when in reality it’s been one of the most stressful times our family has experienced.  Nevertheless, everything we read tells us that half the battle of sickness is maintaining a positive mental attitude.  From the moment we heard of Kelly’s tumor, we entrusted her care into God’s hands.  Your petitions and prayers have helped to cushion her and our family from the awful pain, sorrow and fear that accompanies this scary journey.  But, the journey is not yet over; there is still a ways to go.  We ask that you please continue to pray for Kelly’s quick and complete recovery.  
Kelly told us that when she went into her pre-op MRI, she broke down crying and couldn’t stop.  She quickly started praying and begging God to hold her tight in his arms.  Soon she was flooded with good vibes and started to think, “Why am I crying?  Everyone is praying for me, I am surrounded by loved ones and I have a hospital full of friendly people reaching out to help.”  Shortly, she started to feel enveloped by a renewed confidence.  She came out of that intimidating MRI machine smiling at the technician.  He proceeded to say that he had never seen someone with such a positive spirit and so much family presence at the hospital.  He asked her how she accomplished her good cheer.  She told him about all her wonderful loved ones and the messages she got daily on her blog and e-mails and how so many people were praying for her.... this was a great part of what inspired her to move forward with high spirits.  He thought that was so cool and wished more people would look at it that way!
Kelly and family knew the details of her operation before she went into OR.   When you hear some of these details, you will wonder how she kept her chin up so high and you will realize that the energy force to go forward in such a positive manner came from the incredible support that she has received from all of you.  Do you know that to date, she has received over 7,000 hits on her blog which was opened on October 14! There have been prayer groups going on all around the world.  The response has been daunting.  
So many of you have been asking for more details, so, as difficult as it is to write about this, here is a description of what Kelly has gone through so far, information that was explained to us before the operation (and forgive me if I say something incorrectly, but it’s as close to what I remember as possible): 
We were told that brain operations are the least painful of all operations because the skull and brain do not have nerves, only the scalp has nerves and you don’t have muscle and ligaments to cut through.  The process is as follows:  
  1. The resident medical team, not the surgeon, prepares the head for the operation. They shave a very small strip of hair where the cut is to be made. The cut for this particular tumor extends from the top part of her Right ear slightly over the meridian line. The scalp is cut and  then both sides of the scalp are folded over to expose the skull. They drill holes to form an ovular pattern over the location of the tumor and then they cut between these holes using an electric saw instrument.  The skull section is temporarily removed.  
  2. The neurosurgeon, Dr. Stieg, then takes over and does his art work, the careful and skillful removal of the tumor and its many tentacles.  
  3. Once the tumor is removed as thoroughly as possible,  the surgeon’s job is over and the resident doctors clean up and close the wound sealing the area with a metal plate and staples.  A drainage tube is attached and a monitor is inserted to measure the brain pressure.  She is under close observation for about 2 hours after the operation and then she is taken to Neurosurgery ICU for 24 hours of constant monitoring and care.   
When we heard about the procedure, naturally, we freaked out!... but then, we got down to the common sense level of reasoning and realized the operation was really just as gross as breaking your leg or arm while skateboarding and being opened up to have the bone reset with staples and metal plates inserted.  Once we saw it in this light, we could emotionally handle the details of the operation. Medicine now a-days is truly amazing.  
We have been told over and over again by the experts that Kelly is very lucky because the tumor was on the Right side of the brain and science still doesn’t know much about what this side of the brain controls.  If it had been on the Left side of the brain, she would likely have had some serious side effects, maiming her for life.  
Based on it’s huge size, this tumor has been living happily on the Right side of the brain for many years and it hasn’t been affecting any of her life functions.  As a matter of fact, if you look up oligodendroglioma (oli-go-dendro-glioma) you’ll see that this is a tumor that lives inside of a person’s brain usually from childhood, growing little by little until it finally makes it’s presence known with a seizure.  This is exactly what Kelly experienced!  The average age level when it makes it’s presence known to the world is age 36.  Kelly’s tumor announced it’s presence at age 29, which is good because the younger you are, the better and quicker the prognosis for recovery.  
Thankfully Kelly’s operation is a thing of the past. She’s on medication that controls the pain and other than that she feels wonderfully well.  We now sit waiting for pathology to give us their results.  We should have their diagnosis by Friday.  Everyone assures us that there is a very good chance that the tumor is benign because cancer doesn’t co-exist for a long time in our bodies without bringing major health problems.  Kelly has never had any symptoms beyond the seizure on October 8.  But, as we all know, life can bring all kinds of surprises...so we beg you to please CONTINUE with your prayers; only half the battle is behind us.
We also need your continued prayers because there is one more serious worry.  Glioma tumors send out tentacles (roots), and these tumors can return at a later date.  In other words, if any tentacles or oligo cells are left imbedded in surrounding tissues, the tumor may regenerate.  She will be given another MRI on Friday to determine if all the glioma cells were removed from her brain.  The results of the MRI and biopsy on Friday will determine is she needs to undergo radiation treatment.  If so, the radiation can take anywhere between 5 days and 6 weeks.   We pray that there will be no reason to require further testing and treatment.
The good news is that medical science has advanced so much that the radiation can now be focused to concentrate on a specific location of the brain....area-specific radiation.  Kelly agrees with us that if the doctors decide she needs radiation, she will march forward and into treatment with confidence in God’s love and the best of medical care.  The important thing is that she comes out of this cured and healthy.  
We will continue relaying information and updates of progress whenever we have the chance.  
Your messages and prayers have been some of the most powerful instruments to Kelly’s PMA before and after yesterday’s surgery.  Our gratitude for your “continued” prayers and messages of love go beyond words.  We are truly blessed to be surrounded worldwide by people who love and care for Kelly (and us).  Every day she reads, giggles and enjoys the multitude of notes sent via her blog.  We thank you from the bottom of our hearts.  You have been wonderful!
Besos y abrazos grandes,
Mari and Mark

Tuesday, October 26, 2010

Egg-less determination

Oh the happiness!
Apparently Kelly is up walking and talking!!!!!!!!  The nurses say this is the fastest recovery they have seen; it is very rare that a brain tumor patient gets up immediately after surgery!  She literally just arrived from the O.R. into her recovery room and is already moving around as if nothing.  That sister of mine...is a miracle :)

Moma and Pops just went in to visit her!  Hector is next...and then me!!!  I can't wait!

P.S.
I think that the definition of PMA needs to add an additional meaning: KELLY "The Warrior" DILLON

Two and a Half Eggs

Dr. Sieg and Rabbi Laser called us into the conference room about 20 min ago...Kelly has won the battle!  The tumor was much larger than we were told in Panama...it was actually about the size of a grapefruit (or two and a half eggs)! The doctor says she has had it for MANY YEARS. For the next 24 hrs she will be in ICU and then for 3-5 days under observation here at the hospital.  After that, we will head back to up-state NY for 14 days so that she can rest and recuperate.  

So, pop that bottle of champagne and celebrate her victory! I can't tell you the last time I have felt this way.  Actually, I don't think I have ever been happier :)  As I look around the waiting room, I see radiating smiles of happiness and relief on the faces of ALL our family members.  

THANK YOU FOR YOUR PRAYERS Thank you for your PMA Thank you thank you thank you...
Much love
ani

The battle line has been drawn.

At 7:45am our WARRIOR PRINCESS entered into battle.
We await for her victory anxiously here in the waiting room...

I wish I had the words to tell you how amazing she is...I have learned so much from her these past few weeks. It is hard to explain to you what a true example of strength and courage she has been up to this point.

I will keep you posted throughout the day...

Please do not BBM the family today or tomorrow or the next day!...it gets a little crazy with all the *PING*ing. That was one of the original reasons for this blog. So please please please just follow up on the blog. :) thank you

Friday, October 22, 2010

On Tuesday October 26, 2010...

Kelly will be admitted to the hospital at 5:45 a.m. for her pre-operation MRI, which will be followed later that day by the operation.


That afternoon, Tuesday, October 26 at 5 p.m., St. Mary's Church in Balboa will be holding a special Mass for Kelly.  We would love for friends and family to come together at this time in prayer.  Kelly's best friend, Yoela, and her mother, Tia Maggie, have made this prayer union possible, for which we are so grateful. As soon as we know the outcome of Kelly's surgery, I will be in touch with Yoela so she can bring you up to date on Kelly's post-opt information.


As we read comments made by friends and loved ones, we bask in all the fun memories and delightful stories that you bring us about your experiences with Kelly throughout her life.  We are ever so grateful for having been blessed with someone in our lives who has such amazing energy, high spirits, and good health! This tumor will soon be a thing of the past, like one of our unexpected tropical storms.  We are sure that as soon as it passes, there will be once again lots of beautiful sunlight and blue skies overhead.


She is my warrior of warriors...both my strength and my weakness...for her I would do the impossible.


Please keep up the PMA (Positive Mental Attitude)!
Love, Ani

Doctor's, Rabbi's, and Family...Oh My!

Good Morning beautiful people :)
   Yesterday (Thursday Oct 21) mama wrote this update for you guys, but of course I had a bit of trouble settling into a new internet connection up here in the mountains so I was unable to post...no worries though, that is no longer an issue!  I promise that I will be posting something EVERYDAY from here on out.


So, here is my mama's message:


   Hi All, It's been crazy! But finally all is moving ahead smoothly. We spent all of yesterday (Tuesday Oct.20) in the hospital taking exams, meeting with doctors and trying to get the insurance connected with the hospital. Finished all this and we are now headed to upstate NY to Mountainville, Mark's brother's home for the weekend. Kelly continues in good spirits and we're moving ahead with lots of love and laughter.  The doctor says the tumor is a real biggy but he continues positive with his prognosis. There is a possibility that she may need approximately 6 weeks of radiation to assure all the tumor cells are removed after the operation.  Apparently she's got a kind of tumor whose cells reproduce, so if any trace of cells are left behind, the tumor will return. But, as all the doctors have said, everything is speculation until they get a sample to the lab.  No matter what, we know she is in very good hands and the professionals around her are super friendly and caring. It's been almost two weeks since Kelly's seizure, and we have been going non-stop. We can't wait to get to Mountainville, unpack and relax.  We have 5 more family members arriving on Saturday: Ian and Mary (My oldest child and his wife); Thomson (Ani's boyfriend); Suzanne and Ryan (My sisters daughter and her husband, both great friends of Kelly). Can you imagine getting everyone mobilized to move in the same direction! Whoa, some fun! 
In other news...
Dr. Stieg, Kelly, and Rabbi Goldwesser after her consultation on Wednesday Oct.20 
   The Dillons have adopted a new family member, Rabbi Goldwesser! He has guided us every step of the way from the first moment when we connected with him on Monday, Oct.11, shortly after Kelly got the results of the MRI.  We love him for all his very special attention!  He's been holding our hands so caringly through the worst of the storm and will be there with us to the end.  Ani has become his dear buddy and the two of them get along, royally entertaining all of us in the most serious of moments with their ongoing wise cracks and amusing opinions!  Ani announced today that she is going to name her first son after him, Laser! So, David Polonsky, thank you for introducing us to one of the biggest hearted, and kind people in the world! We love you, Rabbi (and so does everyone else in the hospital!). Thanks for being there for us. 
~Maria Lydia Dillon


Wednesday, October 20, 2010

Getting the ball rolling....

Kelly's 1st time to the BIG APPLE
The Dillon family has arrived! 
  The taxi man that picked us up at the airport could not believe the amount of bags this crazy familia travels with!  He did say that he wished he was part of our family though...all the noise and laughter kept him in a cheerful mood! Thank you Eric from Ghana AKA Mr. Taxi-man, for being so great to us :) We truly appreciated your PMA!
  After unpacking and settling into our hotel room, Kelly decided that she was ready for a banging Thai dinner.  So, after consulting with the concierge, Jonathan, we walked a few blocks to an amazing restaurant on 2nd Ave. in between 72nd and 73rd St. called Viang Ping.  Let me tell you what, that food was GOOD!  So good that we didn't have any room for desert, which is rare in our family...desert is tradition after dinner.
  So, now that I have caught you up to date, I just wanted to say thank you for all your prayers and positive thoughts.  We feel them all around us, filling us with joy and happiness every step of the way. Well, we are off to Kelly's first appointment with Dr. Stieg over at the Presbyterian Hospital and then maybe a nice walk through Central Park. Much love
Ani

Sunday, October 17, 2010

"It's all about the PMA"

Buenos Dias family and friends,
  I wanted to just write a quick note letting you know how truly blessed we are to have so much love and support during such a time as this.  Thank you for your words of kindness, inspiration, and hope. Kelly is doing wonderfully, she is holding strong and pushing forward, and all of our love and support is helping tremendously! Please keep sending her all the positive vibrations you can...like my boyfriend Thomson said to her yesterday on a phone call from California, "It's all about the PMA (positive mental attitude) Kelly"!  So on that note, I leave you in order to get ready for the Dillon family tradition of sunday waffles at mom and dads.  This sundays feast is extra special because our primas Gianna and Michelle are joining us!

xoxo ani 

P.S. Kelly best friend and cousin, will be joining us in NYC to make sure that she continues to feel and live life this happy...
Suzanne and Kelly


Friday, October 15, 2010

Mom just called with good news!!

Latest update:
10 Neurosurgeons at NY Presbyterian Hospital, to include the chief of the Department, just reviewed Kelly's MRI images.

They bring us great news:
-It appears to be a primary brain tumor (glioma ) which is a low grade brain tumor..... very good news!
-There is a very good chance that Kelly will come out of the operation in perfect health.
-The doctors all agree, they don't think this will be a serious case. 
-It should be a successful operation, but they will only know this for sure after they remove the tumor.

So here's the plan:
Tuesday, Oct. 19......... Kelly and family will fly to NY
Wednesday, Oct. 20 ....Kelly meets with Dr. Philip E. Stieg,            
                New York Presbyterian Hospital
                Weill Cornell Medical Center
Tuesday, Oct. 26..........Kelly is operated

KEEP THE PRAYERS AND POSITIVE VIBRATIONS ROLLING HER WAY! (You should see how big her smile was when we heard the news!!)

Xoxo
ani

A beautiful letter from one mother to another...

Dear Mrs. Dillon,
   I am not sure you remember me, but I have had the pleasure of meeting you a few times at MDA functions, as well as at the school itself.  It was always my pleasure to see you and your energy and sense of purpose.  In a recent conversation with Jenny, she mentioned that your family is going through some difficult medical issues.  I hope you don't feel I am imposing on your privacy.  But from one mother to another I just wanted to give you a hug through this e-mail.
   None of us ever know what life has in store for us.  The winding road on the journey of life...  We are all here to grow and to progress and for our spirit to soar.  Only G-d knows how we need to do that.  Our Sages tell us of a potter who, when advertising the strength, endurance and durability of his wares, would tap on them and bounce them around.  For obvious reasons, he would only choose his choicest and strongest and finest.  And when they withstood his banging and prodding, he could safely say that he had created a product of very high quality.  Of course, this is just an example.  Of G-d and mankind, His most astounding wares.  And   in order to show the durability and temerity and the outstanding beauty of the souls He created, He may bang and prod.  But the human soul can prevail.  And when it does, it is declared G-d's finest products...  
   I'm not sure we ever spoke about my youngest child.  He was born with chronic renal failure and from his first day on earth, his life has been nothing but a struggle and a challenge.  We were at death's door more times than i care to remember.  He had a kidney transplant at the age of one and a half  and although we live in the frightening world of medical treatments and scrutiny, that child is our greatest gift.  Today he is G-d bless him, six and a half years old and he is my daily inspiration.  
   Somewhere in our lives, it becomes clear that we are here on a mission.  Our journey in this world is neither random nor coincidental. G-d has some clear objectives for us.  Only we don't know what they are.  And we certainly do not know who we can become.  My heart goes out to you and your family for the fear and the uncertainty you face today.  But dear friend, this is the first day of the rest of your life.  This is when you learn about how wonderful life really is.  And how precious.  Because life does not end with a frightening diagnosis.  But rather, that is when it truly begins.  Illness can be as much a gift as a challenge.  This is when you learn that the only real cure is care and compassion.  And where one may not always be possible, the other, by the Grace of G-d, always is.  This is the time when you discover that even the darkest skies has brilliant stars.  And when you learn to live the moment and relish in the joy of routine and simple things.  To not just live under the sky, but to look up at the stars.  And to see and feel the extraordinary-especially in the ordinary.   This is the time when we learn that the best things in life are not things.  You will learn to live the day for we will never get another one like it.  We learn to love all we can and relish in the miracle of each other.  And we are reminded that unconditional love and acceptance are the sole purpose of life.  You will watch the resilience of the human soul and its dazzling beauty.  You will find many things on this arduous, wonderful and sometimes strange journey, but most of all you will find yourselves.  In the mystery of it all, we have been given all we need to make life work - to find G-d and happiness.  Not story-book tales, but genuine lives that make our soul shine.  And although you will find fine, caring professionals in the world of medicine, you will be empowered to know that that there is no one like a mother.  i pray for your ordeal to be over soon, thoroughly and completely behind you.  But may the lessons and the love last on and on.

With great respect,
Very sincerely yours,
Debby Levy

"You think you have it bad Tia Kelly?"



Try having gas while stuck in PTY tranque!
I love you and know you'll make it through this before I even begin to mumble my first words!
~Besos~ Baby Ella Mia Dom


P.S. I also have non-gassey days...check out how beautiful I am :)


Buenos Dias Hermana

It's friday!..and I have a feeling this weekend is going to be AWESOME...you just wait! XOXO te amo

p.s. SMILE :)

Thursday, October 14, 2010

A letter from my mother, to all friends and family...

   With a heavy heart I write to tell you that Kelly and I will be leaving town indefinitely.  We travel to the United States as soon as we have an appointment.  Monday afternoon (October 11, 2010) Kelly was diagnosed with a brain tumor located on the upper right side above the ear.  It's about the size of an egg.  Dr. says it appears to be a slow growing cancer...maybe 6-8 months old, probably caused by a genetic cell reproduction malfunction.  They have to remove the tumor, see if it is malignant and then we go on from there.  If it is not malignant, she might be up and working again in 2 months.  If it is malignant, the operation will be followed by radiation. 
   Kelly had not had any symptoms whatsoever before Friday morning (October 8, 2010).  She's never even suffered from headaches!  That night after Ani's birthday dinner (October 7, 2010), Kelly had a seizure where she lost consciousness and convulsed violently for about 4 minutes.  We called her doctor, Dr. Abouganem and he recommended she see a neurologist: Dr. Dondis at Punta Pacifica.  Dr. Dondis started a series of tests and gave her some meds.  On Friday and Saturday (October 9&10, 2010) Kelly started throwing up, experienced nausea and a blinding headache.  
   The MRI that she took Monday afternoon confirmed that the symptoms are the result of a tumor.  The other tests confirmed that it is probably caused by a genetic disorder.  Dr. Dondis says she needs to be operated right away.  Tuesday night, we met with the neurosurgeon Dr. Dondis recommended, Dr. Sanchez-Cardenas at Punta Pacifica.  As soon as we get the paperwork together (next couple of days), we will head North.  My sister lives in Jacksonville, and that is the number one hospital noted for neuro-surgery.  The number one hospital for cancer is in Texas and the number 2 is in New York.  So, we might start with Jacksonville. Please keep Kelly in your prayers, we are very positive and focusing on a successful outcome.   
Maria