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August 19, 2008.  It was a day of uncertainty for us.  We took Grayson to his pediatrician to see if he could figure out the cause of his headaches and nausea.  Oddly enough, at the time of examination, Grayson seemed to be doing well.  He was acting silly and asking for donuts.  Surely there was nothing "drastically" wrong with him...or so we thought. 

By 3pm we were driving to Plano Presby for a cat scan and spinal tap.  All I remember is the pediatrician telling me on the phone to get to the hospital immediately for testing.  I handed Isabella off to a neighbor as tears streamed down my face and I prepared to hide behind my sunglasses as Michael and Grayson picked me up in front of our house.  The next few hours would prove to be gut wrenching as the diagnosis unfolded.  "Your son has a brain tumor.  And it's in the worst possible place, the brain stem."   

Picture a computer when a storm strikes and it suddenly shuts down and goes black on the screen.  That's what happened with my body and spirit when I heard those words.  Everything went black in the room.  I thought, "Surely this is a bad dream and I will wake up any second."  But it was "real."  This was happening. 

Our lives were about to change forever.  I can remember the grip of my husband's hands on my shoulder and his brave, confident look as he said to me, "We can do this Christina.  God has given us an opportunity to shine, and he has entrusted us to walk through this with faith in him as the creator of this universe."  I must say I wasn't in the place where I could say I could see this turning out for good.  But it did turn out for good... in more ways than we had ever imagined. 

This morning, Michael and I sat across from a commercial real estate agent and a developer.  Our hope is to plant a church in or nearby the Addison area.  Nothing is set in stone at this point, but the initial introductions to the ideas and concept of a church being included in this area of the city were made. 

Michael and I then headed North to meet our banker to sign the papers for our Summit Life Church bank accounts.  And as I signed my name on each of those papers, I was speechless - something Michael rarely experiences!  My mind was recalling all that occurred 365 days ago.  How did a year go by?  How did my kids get so tall?  How did my youngest, Isabella get old enough to go to Kindergarten this morning?  How did God heal Grayson of 2 major surgeries completely removing a tumor from his delicate brain stem with no residual tumor being seen on the recent MRI's?  And honestly, did it really even happen?   

It seems so far away now because now is about building a church so that we can touch hearts, transform lives and teach people about and for the Kingdom.  Now is about signing papers and filing legal forms and getting on our faces to ask God what he would have us do next.  Now is about forming committees, board members, group leaders and a staff.  Now is about experiencing another miracle in our lives.  Now is about walking into our destiny.  Now is about Michael being the pastor of his own church in the Dallas area. 

365 days ago we were scared senseless.  And while I guess you could say we have days now that we are wondering how all this will unveil itself, we know without a shadow of a doubt that Super G's diagnosis and the months to follow were just preparation for the "now" in our lives.  It literally catapulted Michael into this next level of leadership and vision for the Kingdom of God. 

The miracle was around the corner for us in ways we could never have imagined.  Your trials will prove to be the same if you will lean on God and never let go.   

Summit Life Church...The adventure of transformed living starts here.  Perhaps we should think about changing the tag line because for us, the adventure of transformed living started 365 days ago!  

Standing in awe of His goodness, Christina

Send Michael an e-mail at- s
ummitlifechurchpastor@gmail.comFollow the adventure of launching Summit Life Church- www.summitlifechurch.com
Send Christina an e-mail at- cperron11@tx.rr.com
Follow Christina on Twitter- @cdelperron
Become her friend on Facebook- Christina DeLaGarza Perron



 


 
 
 
 
 
 
5/29/09
  Today was the last day of school!!!!
we had a party we also had ice-cream! and my mom and dad will buy me falcon EBF 25. wich is a gun
love grayson
 
 
 
 
 
 
Today was the big 6 month MRI.  Hard to believe it's been 6 months since Grayson's craniotomy.  It was an important marker for us knowing that the 3 month MRI was a little soon for anything to happen, if anything were to happen. 

We were pretty hopeful the MRI would show us that they got all the tumor and that none of it had grown back.  What we weren't sure about was the residual hemorrhage that was substantial in size at the 3 month MRI.  The surgeon told us that it "normally" takes 9 months to 18 months for the body to re-absorb the post surgery bleeding.  Because of this, she had warned us that he might not be allowed to play any sports this spring or next fall. 

We entered her office and before we even had a chance to sit down, she said, "It looks great."  Once again, the news was outstanding.  Not only did the MRI show that the tumor is completely gone and no signs of growth again, but the hemorrhage (which was about the size of a dill pickle) is now down to 1/10 of a centimeter!!  Practically nothing is there!!  She shook her head and said that Grayson was "way ahead of his healing time" and that she didn't know what to say.  Of course we jumped right on that and said, "We know what to say - Praise the Lord!"  :) 

Then Grayson piped in and said to the surgeon, "Do you know what happened to the spot in my head?  Jesus took it out, threw it in the trash then grounded it up and sent it back to Satan!"  

We were all stunned at his statement.........out of the mouths of babes!!  

Thank you again for all your prayers.  We are rejoicing and overwhelmed with gratitude for the miracle God provided for all of us.  

Blessings, Christina, Michael, Grayson and Isabella 
 
 
 
 
 
 

Last week we received a letter in the mail from Children's stating his scheduled appointment for his next MRI. 

I was in the car with the kids when I pulled up to the mailbox. I saw the little red balloon and immediately opened the envelope to see what it said.  (My heart always skips a beat when I see that envelope.)  At the top, I noticed that his next MRI would be done "without" contrast.  I had to read it twice to make certain I read it correctly.  In other words, no need this time for an IV.  Sounds like such a small thing, but it's HUGE to an 8 year old!  I looked back and told Grayson the wonderful news.  He looked at me so peacefully with a sparkle in his eye and said, "Mom, FINALLY, no IV!"   

Grayson is now facing a couple of new giants in his life.  And he's using his own trial to stand in the gap and pray for his 2 friends who have been attacked with cancer.  Their names are Connor and Cody. 

Connor is in 2nd grade with a stomach neuro blastoma that is malignent.  Recently, a new tumor has grown and we found out Thursday that it is growing rapidly.  This has been close to a 3 year battle for this family. 

Cody is Grayson's football hero from the PCA high school team where Grayson attends school.  Cody came to see Grayson several times in the hospital; brought him cookies his mom made; and even gave Grayson a varsity jersey signed by all the players.  It was the first smile we saw on Grayson's face after he came out of surgery.  I won't forget that day as it brought us hope that Grayson would smile again and would arise out of that bed one day soon.  Cody even came over to babysit the kids so that mom and dad could have a lovely night out - a real date!  Grayson talks about Cody all of the time.  Then 2 weeks ago Cody was diagnosed with a malignant tumor in his glute and has begun chemo.  It's agressive and we had to break the news to Grayson.  

"Super G-man" says his prayers at night for his two friends, and does it with such conviction and passion.  A conviction and passion that only he could have as he has walked through the shadow of death himself.  He shuts his eyes tight and says, "I know you can heal Connor and Cody Lord.....just like you did me." 

So for these two boys, we ask that you join us in prayer for complete healing.

Blessings, Christina
 
 
 
 
 
 
We have a prayer petition for anyone that visits Grayson's blog.  It is for his buddy, Connor, who is in 2nd grade with Grayson and has been battling stomach cancer for over 2 years now.  Below is a short bio and an update from him mom, Joy. 

Joy and her husband Tait were such prayer warriors for us during out crisis with Grayson. They met with us, prayed for us, and were willing and available for questions 24 hours a day.  God certainly used them to bring comfort to us during our greatest time of need. 

My heart is so very heavy for what they are now going through, yet when Grayson prays for him at night he saids it with such ease and confidence; "And Father, just heal Connor."  As if to say, "Hey God, it's no big deal for you to heal him, so go ahead and do it.  Child like faith....so refreshing. 

Please read his story and add this family to your prayer list.  You can stay up with his latest news on www.teamconnor.com

We are asking and believing for a miracle on bended knees.

Blessings, Christina

=============================================================================================================
Connor is eight years old. He loves all Super Heroes,
riding his bike and dueling with toy swords and light
sabers. His favorite color is green. His favorite foods
are pizza, shrimp and s'mores.

Connor is such a good boy! His proud parents are Tait
and Joy Cruse. Connor is little brother to Mackenzie,
age 11, and big brother to Carson, 7 and Mason, 2.

On May 15 2005,  after periodically complaining of a
mild tummy ache for two weeks, Joy took Connor to the
hospital. She was worried Connor might have
appendicitis, since she did as a young girl. After a day
of tests, Joy and Tait were stunned to learn Connor
was very sick. He was diagnosed with Stage 4
Neuroblastoma.

Neuroblastoma is one of the most common solid
tumors of early childhood usually found in
babies or young children. The disease originates in the
adrenal medulla or other sites of nervous tissue. The
most common site is the abdomen (near the adrenal
gland). Most patients, including Connor, have
widespread disease at diagnosis.

Connor is currently undergoing treatment at Children's
of Houston. His current treatment  protocol means he
goes to Houston every six weeks or so for several days.




This small stomach is sure causing problems. He gets full so quickly, and then he gets a
stomach ache and/or throws up a little bit. We are not making much headway in this area.
PLEASE PRAY THAT HIS STOMACH WOULD HEAL, HE WOULD BE ABLE TO TAKE IN MORE
CALORIES AND HE WOULD GAIN WEIGHT. PRAY WE CAN MAKE THIS PROGRESS
WITHOUT THESE STOMACH ACHES. It is very frustrating to deal with this everyday, with
everything else that is going on.

Connor's scans will be February 19 in Houston. We should have a treatment plan by then.
PLEASE PRAY THE SCANS SHOW NO GROWTH WITH THIS NEW AND OLD TUMOR. PRAY
FOR GUIDANCE FOR CONNOR'S TREATMENT(S). We are still investigating alternative
medicine approaches that will complement the conventional therapies. There are so many
different directions that it is overwhelming to me at times. I am asking for WISDOM, as King
Solomon did. PLEASE PRAY FOR WISDOM/DISCERNMENT FOR US.

My friend, Mary Kim Gray, said this story of Daniel in Daniel 2 reminded her of our situation
and our search for wisdom.
Daniel was asked by the king to interpret his dream. If not, he and his friends would be
executed. God answered his prayer and He showed Daniel the meaning of his dream. This is
Daniel's prayer in response to God's faithfulness.
'Praise be to the name of God for ever and ever;
wisdom and power are his.
He changes times and seasons;
he sets up kings and deposes them.
He gives wisdom to the wise
and knowledge to the discerning.

He reveals deep and hidden things;
he knows what lies in darkness,
and light dwells with him.

I thank and praise you, O God of my fathers:
You have given me wisdom and power,
you have made known to me what we asked of you,
you have made known to us the dream of the king.'"

As Kim is doing, please pray Daniel 2 for us--that God would reveal deep and hidden things
and that the light that dwells with Him would be given to us, so that we can walk in it as we
seek the perfect treatment plan for Connor. Praise God that all wisdom and power are His,
and plead for mercy with us that God will give Connor perfectly restored health.

Still Believing,
Joy Cruse
 
 
 
 
 
 
We have a prayer petition for anyone that visits Grayson's blog.  It is for his buddy, Connor, who is in 2nd grade with Grayson and has been battling stomach cancer for over 2 years now.  Below is a short bio and an update from him mom, Joy. 

Joy and her husband Tait were such prayer warriors for us during out crisis with Grayson. They met with us, prayed for us, and were willing and available for questions 24 hours a day.  God certainly used them to bring comfort to us during our greatest time of need. 

My heart is so very heavy for what they are now going through, yet when Grayson prays for him at night he saids it with such ease and confidence; "And Father, just heal Connor."  As if to say, "Hey God, it's no big deal for you to heal him, so go ahead and do it.  Child like faith....so refreshing. 

Please read his story and add this family to your prayer list.  You can stay up with his latest news on www.teamconnor.com

We are asking and believing for a miracle on bended knees.

Blessings, Christina

=============================================================================================================
Connor is eight years old. He loves all Super Heroes,
riding his bike and dueling with toy swords and light
sabers. His favorite color is green. His favorite foods
are pizza, shrimp and s'mores.

Connor is such a good boy! His proud parents are Tait
and Joy Cruse. Connor is little brother to Mackenzie,
age 11, and big brother to Carson, 7 and Mason, 2.

On May 15 2005,  after periodically complaining of a
mild tummy ache for two weeks, Joy took Connor to the
hospital. She was worried Connor might have
appendicitis, since she did as a young girl. After a day
of tests, Joy and Tait were stunned to learn Connor
was very sick. He was diagnosed with Stage 4
Neuroblastoma.

Neuroblastoma is one of the most common solid
tumors of early childhood usually found in
babies or young children. The disease originates in the
adrenal medulla or other sites of nervous tissue. The
most common site is the abdomen (near the adrenal
gland). Most patients, including Connor, have
widespread disease at diagnosis.

Connor is currently undergoing treatment at Children's
of Houston. His current treatment  protocol means he
goes to Houston every six weeks or so for several days.




This small stomach is sure causing problems. He gets full so quickly, and then he gets a
stomach ache and/or throws up a little bit. We are not making much headway in this area.
PLEASE PRAY THAT HIS STOMACH WOULD HEAL, HE WOULD BE ABLE TO TAKE IN MORE
CALORIES AND HE WOULD GAIN WEIGHT. PRAY WE CAN MAKE THIS PROGRESS
WITHOUT THESE STOMACH ACHES. It is very frustrating to deal with this everyday, with
everything else that is going on.

Connor's scans will be February 19 in Houston. We should have a treatment plan by then.
PLEASE PRAY THE SCANS SHOW NO GROWTH WITH THIS NEW AND OLD TUMOR. PRAY
FOR GUIDANCE FOR CONNOR'S TREATMENT(S). We are still investigating alternative
medicine approaches that will complement the conventional therapies. There are so many
different directions that it is overwhelming to me at times. I am asking for WISDOM, as King
Solomon did. PLEASE PRAY FOR WISDOM/DISCERNMENT FOR US.

My friend, Mary Kim Gray, said this story of Daniel in Daniel 2 reminded her of our situation
and our search for wisdom.
Daniel was asked by the king to interpret his dream. If not, he and his friends would be
executed. God answered his prayer and He showed Daniel the meaning of his dream. This is
Daniel's prayer in response to God's faithfulness.
'Praise be to the name of God for ever and ever;
wisdom and power are his.
He changes times and seasons;
he sets up kings and deposes them.
He gives wisdom to the wise
and knowledge to the discerning.

He reveals deep and hidden things;
he knows what lies in darkness,
and light dwells with him.

I thank and praise you, O God of my fathers:
You have given me wisdom and power,
you have made known to me what we asked of you,
you have made known to us the dream of the king.'"

As Kim is doing, please pray Daniel 2 for us--that God would reveal deep and hidden things
and that the light that dwells with Him would be given to us, so that we can walk in it as we
seek the perfect treatment plan for Connor. Praise God that all wisdom and power are His,
and plead for mercy with us that God will give Connor perfectly restored health.

Still Believing,
Joy Cruse
 
 
 
 
 
 
Lately, so many have come up to us and asked (or commented) on how they bet we are so pleased to see 2008 behind us. 

In some ways, we would say yes.  But in other ways, we'd have to say no.  Truth be known, I don't think we've ever been so close to God the way we have been throughout this crisis.  It brings new meaning to the verse in Isaiah that says;

"For I will pour water on the thirsty land, and streams on the dry ground; I will pour out my Spirit on your offspring, and my blessing on your descendants."  Isaiah 44:3

We were so very thirsty to hear from the Lord.  There and only there was our hope.  And God literally poured out his spirit upon us to get us through it all.  Crisis have a way of doing that.  So be encouraged if you are going through one in your life!  Because with God, you WILL  prevail.  (And by the way, I am speaking of God the fatherThe one and only father that we have personal access through Jesus.  The bible tells us that He is the way, the truth and the life, and that nobody will come to him but through his son.) 

The next verse in Isaiah says:

"They will spring up like grass in a meadow, like poplar trees by flowing streams."  Isaiah 44:4

This past week we have really settled in and are beginning to feel like it's spring outside.  (Being a native Dallas girl, I know all too well that the weather can turn on a dime so I won't get too attatched to it!)  But I am really speaking metaphorically about spring in our lives right now.  It "feels" like a new beginning with new green grass and life all around us.  

And we just so happen to be solidifying our 10 day cabin trip for June in South Dakota.  We can't wait to see beautiful pine trees that will be towering over the flowing stream that runs in front of the Cabin.   

For those of you who do not attend prestonwood and haven't had a chance to see this during service, below is a link to view the Prestonwood Baptist Church 2008 year end video.  And guess who made it in the spotlight for a few POWERFUL seconds?  You got it, our very own "Super G-man!"  He shows up about 3/4's of the way through.  He is holding up a sign that says it all.....literally!  (Taken from Cardboard Testimonies done at church in October.)   

Enjoy ;)  Christina

http://www.prestonwood.org/updates/video_yearend2008.php
 
 
 
 
 
 
It was a long day today at Children's.  Seemed longer than all the other times we had MRI's.  Not sure why, but we are certainly relieved it's over.  

Grayson was so brave and patient yet once again.  At 3pm the surgeon came in and said, "I have good news and bad news. Which do you want to hear first?"  Time froze for Michael and I as we looked at one another with disbelief.  Actually, it was a look of panic on our faces.  My tongue was stuck.  I don't even think we answered her.  All of the sudden she chuckled and said, "Don't worry, the scan of his head is perfect.  The bad news is I will not get to see you guys as often since i will be moving him to have MRI's every 3 months instead of 6 weeks! 

As you can imagine, we both exhaled and "tried" to chuckle with her.  Michael said he had to sit down before he became ill!  She walked us through all the scans from prior months and compared them to today's.  Everything is healing well and surgery swelling is reducing nicely.  The little bit of bleeding showing up from post-op grew a small amount, but it's most likely due to his sledding accident from Christmas.  She said we'd keep an eye on it, but she's not worried about it.  (Michael was kicking himself, yet again for not putting that helmet on Grayson) 

We are so relieved that our Super G-man is still super!  For that, we are eternally grateful.  But he will have to be "super" from the bleachers because she informed Grayson that he cannot play baseball this spring season.  He was bummed for a few minutes, but then got over it.  Mom and dad are completely ok with it and trust her judgment wholeheartedly.  We just happened to mention it and really never even though twice about him not being able to play.  She said she was very thankful we discussed it.  I guess it's difficult to remember that it's only been 12 weeks since that long surgery day and his head must have more time to heal

We are definitely feeling the stress from the day and are exchanging yawns as we sit here on the couch.  I noticed today (I think I was more in touch as opposed to being in shock the times before), that each time we go back there, my mind re-lives all the moments from the surgeries before.  We walk the same halls; see the same personell; take the same elevators; and even feel the same anxiety when you see just how many children are there sick.  It took my breath away today.  It made me realize how little control we really have over anything in this world. 

One thing is for sure, we will rest peacefully tonight knowing he's on the road to recovery.  Thank you for all your prayers this week and we ask you to continue to pray for his complete healing and most importantly, protection from accidents or illnesses.  Oh, and if you get a little extra time, please include all the children that come in and out of those doors at Children's hospital.  Some with hope, but so many with none. 

Peace and Blessings,
The Perrons


 
 
 
 
 
 

It's been a while and I have a lot to tell.  I'll fill you in on Christmas today, and then a couple more blogs this week.  We had one last big lesson to learn before 2008 ended.

The Christmas season was magnificent.  It will be etched in our memories forever.  Everything felt different and looked different.  We worshiped differently, we loved others differently, we "believed" differently.  We are blessed in that we will never be the same after a crisis of this magnitude.   

Christmas morning was fun, to say the least.  At the top of Super G Man's Santa list was a Nerf gun super blaster; Ultimate Band for Nintendo and Wii; and a Havoc Heli laser bug battle-copter.  Santa certainly delivered and even left Super-G a note stating that he had heard of his surgery and his miraculous recovery.  Grayson lit up as he looked at the plate of goodies where the reindeer had taken a few bites of the carrots and noticed there was a HUGE bite taken out of the cookies.  There were crumbs everywhere!  The kid's faces were priceless....Santa marked his territory for sure!! 

We headed to Minnesota that afternoon to spend some much needed time in the frozen tundra where Michael's family lives. We were ready for cold and snow and a white Christmas.  We got that white Christmas.  There was plenty of snow on the ground and all through out dinner the kids had only one thing on their minds......playing in the snow!  Grandma was well prepared with new ski jackets, pants and gloves.  They looked like they were ready for the arctic! 
 

A couple of days later we headed for the "big hill" in Burnsville with Uncle Todd, Aunt Shanny and their cousin, "CC."  And this wasn't some old ordinary hill.  This was and will be remembered as the one that initiated mom into the "crash and burn into the bushes while sledding on a saucer" hill!  Needless to say, that was mom's "one and done" for the day!  But Super G, Isabella, and Dad flew down the hills numerous times before deciding to go in.  I sat there in total amazement of how just 8 weeks prior, Grayson was curled up on that hospital bed not even able to speak.  And here he was laughing and giggling and screaming, having the time of his life.  He got a little over zealous and wanted to go down alone, but that was not allowed!  He begged, pleaded and whined (not for long) until his dad got firm with him and reminded him that his head was still healing. 

The next day came and dad took the kids to a smaller hill down the road from Grandma and Grandpa's house.  I stayed back and caught up on my sleep!  They returned rosy cheeked with smiles from ear to ear.  Another successful sledding day.......or so we thought.

8am Tuesday, Grayson walks into our room and announces, "Mom, dad, the back of my head feels a little wobbly."  I looked at Michael and his face turned grey.  Grayson confessed that when he went down the hill "by himself" the day before, and "without a helmet" he spun out and knocked the back of his head after crashing through some bushes. (None of this had been mentioned to mom the day before.) 

So off we went to the emergency room.  5 hours later they released us.  They took a cat scan of his head to make sure there were no broken bones in the skull.  But they couldn't release us until they spoke to one of the surgeons in Dallas to confirm that the slight movement of the mid-line they were seeing in his cat scan was from his prior surgery and not the incident at hand. 

Michael felt so bad and I knew it.  No helmet and going down the hill by himself makes for a scary lesson to be learned.  The rest of the trip was spent making snowmen and snow angels....no danger in that!!  When we returned, I immediately took him to the eye doctor.  All was well with his eyes.  A big sigh of relief for us.  Michael called our surgeon and she laughed and called Grayson "a little snow monkey."  All she said was what we already knew to be true....."Next time he MUST have a helmet on!"

Life is about experiences and there are plenty of lessons to be learned along the way.  We realize we can't put him in a bubble for the rest of his life.  We pray that God will give us wisdom on how to live with this situation for the next 10 years.  We don't want to smother him with over protection (mom's tendency) and we don't want to act if everything is fine (Dad's tendency). 

Isn't it amazing how God can continue to teach us things in simple, daily decisions?  Tragedies and crisis are not necessary to learn lessons.  We are grateful that this lesson didn't cause any major damage to Grayson's head.  We believe the angels were certainly protecting Grayson, yet once again.  I would have to say that my verse for the year is this: 
                 "For He will command his angels concerning you guard against you in all your ways."   Psalm 91:11

Happy New Year!  I'll be back with a couple more stories about Grayson; the doors God has opened already in January; and of course an important prayer request for his next MRI, this coming Thursday, Jan. 29th.

 
 
 
 
 
 
"This is as good as it gets."

Those were the words we heard from the mouth of the surgeon on Thursday afternoon as we sat in her office with Grayson, reviewing all 4 of his MRI's taken of his precious head since August 19th.  

The radiology report showed, "no residual tumor remains."  They might as well written on the report, "MERRY CHRISTMAS!"  Talk about keeping "Christ" in Christmas!  Maybe those who still do not "believe" would like to sit as we share THIS miracle story with them?!!  

It's been such a journey.  And we were both apprehensive going into this meeting.  Afterall, it was "right before" Christmas.  What if it had grown?  What if the area wasn't healing well?  Then we'd go right back on the roller coaster, a ride we were not interested in riding again.  

Side bar - It reminded me of when Grayson was 14 months old and we found out we were pregnant.  We were so excited!  It was Christmas and I was about 9 weeks along when we went for the sonogram and there was no heartbeat.  I was devastated.  It was 2 days before Christmas that the DNC was scheduled.  The unfortunate part was that there was "no room in the inn."  The regular hospital surgery rooms that was.  So they told us they would need to do the surgery in one of the delivery rooms.  Well wouldn't you know it, that it was the very same room where Grayson was born about a year earlier.  It was so painful to walk through that.  But I remember thinking to myself, "Christmas is not about me.  It's about Jesus."  That was a new level of faith for me.  That miscarraige was the first of five to come.  3 before Isabella, and 2 after her.  Each of those trials strengthening me to lean more on God and not myself.  Looking back, it was for a reason......it was preparation for a huge trial, one that was already in the mind of God.  And in no way to we believe it's just "coincidence" that the news we received yesterday was news that would be reported "right before Christmas."   

After reviewing and reviewing and reviewing the MRI with her, I kept saying, "So there's nothing left?"  She answered, "Looks that way.  We'll just keep an eye on this area and most likely after a couple more 6 week MRI's, hopefully we'll find that it's boring and I'll move him to do them every 3 months."  Michael looked at me and said, "Babe, you can breath....take a breath.  She said that there's nothing there!"  

Off we went to Starbucks for an extra large chocolate chip cookie for Grayson and a seat for mom while she gathered her thoughts and  tried to keep from getting sick!  Grayson talked to his Grandma on the phone and said, "Hi grandma, mom is about to throw up!"  I guess the anxiety took it's toll ;)  

MERRY CHRISTMAS to each and everyone of you and ALWAYS "Believe" that God has the power to do whatever he chooses to do.  May not always be how "we" would do it, but then again our ways are not HIS ways.  It is God, the creator of the moon and the stars and the one that sets the earth on its axis, who is in control and is able to "trump and stump" everything and everyone.......including initial medical reports that said, "The entire tumor cannot be removed from your son's head."  

Love and Blessings,
Michael, Christina, Grayson and Isabella  

   

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