Wednesday, May 15, 2013

MOTHER'S DAY

MOM'S DAY RUN 2013

May 16, 2013 by Suellen Lindquist

Mom's DAY RUN 2013

My mom didn't know the legacy she would leave. She did say she wished she could do more to raise awareness and money for VHL.

So after she passed away, I made a promise that I would do this.

The Mom's Day Run was born on May 8, 2011. 48 family and friends showed up to run or walk our little race. We raised $1500.

This year was our 3rd Annual Mom's Day Run and 161 people came and we raised $4990! I walked out to the first turn. I wanted to take Starting Line photos and catch shots of the participants as they passed me by. As I turned towards the Starting Line, my eyes brimmed with tears. "Momma, can you believe this?" "Look, what we've done." My heart was overflowing with pride.

I kept a promise...




 

ROBIN

May 16, 2013 by Suellen Lindquist

My sister Robin with my mom and me.

We lost my sister to a tragic accident on March 21, 2013
You never ever imagine getting "that call", that someone you love has been killed
in a horrible accident.

My sister was walking down the street and was hit by a car that lost control.
An awful accident.

My sister and I had a typical sister relationship. We shared a room growing up, we shared secrets...she was my little sister and I miss her so much.

HERE IS THE SPEECH I READ AT HER MEMORIAL

ROBIN ANNE GARRISON
A box arrived the other day. …it was on the counter when I got home. A little brown box about this big. It just sat there, this little brown box. I knew it was coming…and that this was just one stop along way…

Robin was born on a Wednesday morning in the summer of 1962. Mom didn’t want to wait at the hospital when she could wait out her labor at home. She waited till the last possible moment before going to the hospital. She was taken up to delivery while dad filled out the paperwork downstairs. ….Robin didn’t wait…she was delivered before dad made it upstairs.

Robin came into the world with a yell. This tiny, crying, screaming little being would be my little sister. More than that, she was our baby sister. As older siblings, it’s a given that you look after the younger ones. It’s an unwritten rule. So, I made sure she didn’t eat something she wasn’t supposed to, or stick her finger in the light socket. I walked her to school, and made sure she didn’t dress funny. We shared a room, we shared secrets, we shared hopes and dreams. I enjoyed being Robin’s big sister. I liked to believe that I could look after her, protect her…and keep her safe.

Robin was just 4 feet 11 inches tall, (but she would tell you 4 feet 11 ½ inches tall) . She was loud, but not in a negative way…being the youngest, she just wanted to make sure she was heard. She never let you forget that she was the youngest and she enjoyed all the perks with being the baby of the family…and Mom’s favorite.

Some of you knew my sister as Bobbie. If you did, you were in a select group of people. Shana, the oldest of her nieces and nephews started calling her Bobbie, and it just stuck. All of the nieces and nephews called her Bobbie. Some called her: My Bobbie.

If you were in the “My Bobbie” club, you might have had nick names. Like, Honey Bunch, Sugar Plump and she’d end conversations with “Smooches or Toodles”. With Bobbie, you shared exciting adventures. She was loud, she was funny, she was creative, and fun. It didn’t hurt that she was just a little taller than you were. She would build forts with sheets and pillows. She would have water balloon fights, sometimes food fights. She made popcorn and let you stay up late. She would let you watch shows your parents wouldn’t let you watch. She would bake cookies and tell stories that made you laugh until you cried.

She would often catch the kids trying to measure their own height with hers. If you were taller than Bobbie, you were grown up. No matter how old you were. No matter how tall you were, she would wrestle you to the ground and sit on you, and yell “I’m Queen of the Mountain!”…and she was.

Robin was Queen of the Mountain.

I asked family members to give me one word that would describe Robin. In this list, there is one word that will seem out of place. It isn’t…but you’ll have to ask my Uncle Rob to tell you the story behind it. Here is the list:
  • Endearing
  • Funny
  • Loving
  • Scrappy
  • Fiesty
  • Smart
  • Creative
  • Stubborn
  • Sweet
  • Loyal
  • Boisterous
  • Cowabunga
  • Fun
  • Awesome
  • Fearless

My sister was the youngest and she used that to her benefit. When we were younger and often times bored, we’d always look for something to get into. Robin, always a willing participant would join in on the fun. Mostly mischeavious fun but sometimes “we’re gonna get it kinda fun”. When things would get a little dicey, while we were on one of these adventures, Robin (maybe the smartest one of the three) would make it home before me and Steve to tell on us. Mom would be waiting, hand on her hip, tapping her toe…and Robin with that big old grin hiding behind her. Robin never got into trouble, at least that’s how I remember it. She’d probably tell you different, because she was the good daughter and mom’s favorite. Steve and I teased her merclessly, I guess that’s what siblings do.

When we were in our teens, Robin was 16 yrs old, she had a credit card, a bank account, she worked two jobs and was going to school. Out of the three of us, I always believed she’d be the most successful. She was determined, ambitious and confident. She held the world I her hand.

So, how do you measure success? Is it a piece of paper on the wall? Is it your bottom line? Is it material things? I think Robin’s success was in the relationships she made. Her nieces and nephews adored her. And she them.

I read somewhere, that when you’re laying on your death bed, you aren’t wishing that you had spent more time at the office, …I believe the things that are most important are the relationships that you’ve built. It’s the hugs, it’s the” I love you’s”…it’s the time spent. Robin gave that time...

I wish I had spent more time with my sister. I wish I had done a better job at being a big sister.

I asked the kids to share a story about Bobbie. I wanted to share more of who she was. But, there are too many storys to mention. The kids all loved hanging out with Bobbie…she had the ability to make a lot of fun out of nothing and they were the best times.

Robin was loved, she was cared about and she had a family who will miss her so much.

A little brown box arrived the other day…and I will take great care of this precious little box, until I carry it to its destination. I will make sure you arrive safely, then release you into the sea. I will visit you at dawn when I run along the shores, I will see you in the sunset as I walk along the sand…and I will miss you every day. I love you Robin and will miss you very much.


My Mom

May 16, 2013 by Suellen Lindquist




My mom was my hero. She lost her sight at the age of 25, she had 3 small children.
I don't remember her not being blind. I was about 5 years old and I don't think I really understood what was going on...but I remember her being brave and strong...and she kept moving forward. To me, she was invincible.

Later, as I grew older, I would think about how hard life was for her. Raising children is hard enough with your vision. We were brats and I know we drove her crazy. We'd laugh about those days later but, when I had children of my own...I imagined the terror she must have experienced. My mom was amazing.

She was kind, she was gracious, she would give you the shirt off of her back, even if she didn't have it to give, she would give.

We learned about VHL when we were kids...and VHL has evolved from being "just an eye disease" to a "cancer syndrome" We were told if we had no symptoms by the time we were 20 years old...we wouldnt "get it". Interesting statement...because you don't "get it". You have it or you don't.

Fast forward to 1994...I worked for Warner Bros at the time. We had just gotten a new insurance and I was browsing through the book and saw a name I recognized. Dr. Bradley Straatsma (you can google him). He was the same doctor that diagnosed my mother back iin 1962. I had just been seen by an opthamologist a few months prior but made the appointment anyways. Not even an hour into the appointment, I found out that I had VHL. We called in the entire family to get scanned. My brother had it too. Dr. Straatsma would arrange the surgery for my brother, since he had not insurance. We will be forever grateful to Dr. Straatsma and all of the work he has done for us and other VHL patients. UCLA has a VHL Clinic now...this has been a lifesaver.

UCLA is a teaching hospital, so when you have a rare disease...all of the residents come in to take a look. I had my first surgery then. There would be 7 more.

It's a strange feeling when you are diagnosed with a disease. I mean, I always new of the possibilitiy but when you get the actual dianosis, it's a totally different deal. I didn't cry, I didn't get mad, I wasn't sad...not until I heard my mother's voice crack when I told her I too have VHL. I think, she felt responsible... I didn't understand the totality of that moment until, my daughter Shana was diagnosed.

There is nothing worse than knowing you've passed something like this onto your child. And nothing can prepare you for the the terror that each surgery brings. We say our prayers, I try so hard to be strong because my children need me to be strong. They look to me for this strength. I cry when I'm alone...I regroup and I keep moving forward.

We've since learned not to worry about what we can not control. We have a thing in our family that: We do; not worry about it until we have something to worry about. This means...that no matter how many scans they do, or how many times they call you back for a redo, or no matter what kind of face the DR makes...we do not worry until we have something to worry about. We are VHL WARRIORS...we fight one battle at a time. That's what we do.

When Shana had her last surgery in April 2011, it was a terrifying thing since we had just lost our mom to the same type of surgery. I prayed that my mother would hold her in her arms, keep her safe and comfort her. When Shana woke up she said: "Grandma was here, she brushed the hair from my face, like she did when I was little".

And if...that SOMETHING comes up, we gather the troups, we huddle together in prayer, we gain strength from each other and know, that my precious mother is watching over us.

My family is but one...there are so many others out there fighting the fight, no mater what type of cancer it is...no matter what illness. They all need your help.

Please give what you can...every little bit helps.

Thank you xoxo

SIDE NOTE: A few years ago my uncle put a Family DVD together. There were snapshots and video's of our family going back to the 50's. There was one shot, that is seared into my brain forever...a video, of my mother. It was in the 60's, we were small and goofing off for the camera. And then there was this one shot (video) where she was looking into the camera...I've never known what it felt like to have my mother look at me. What a glorious gift...I don't think my Aunt and Uncle even know...but I will treasure that small gift for the rest of my life.
SUELLEN'S FUNDRAISING PAGE

May 15, 2013
KEEPING MY WORD

I promised my mom...that I would do whatever I could to raise money and awareness for Cancer Research. Am I doing enough? I always ask myself that question. Could I do more...? The greatest gift we can give is of ourselves. Our time, our efforts... our help.

My mom passed away on August 2, 2010 from a Cancer Syndrome. Since then, I've helped raise almost $10,000 for Cancer Research. I will keep my promise to do whatever I can to raise money and awareness for Cancer Research.

I am participating in the Team in Training, NIKE Half Marathon in San Francisco. That's 13.1 Miles. I am running to help find a cure. I will run in Memory of my Mom and in Honor of my daughter (who has the same disease).

Did you know that Team in Training has raised over 1.2 Billion dollars for Cancer Research with help from folks like you. You can donate now by clicking the button and donate whatever you can...$5, $10, $20...no amount is too small, because if we all give a little, it will turn into a lot.

Today, I will ask all my friends and family to please donate whatever you can. The need is great, the cause is worthy and someday because of your dollar...we will find a cure!

Thanks in advance for your love and support.

<3 4 Mom

xoxo, Suellen

__________________________________________________
This makes me want to STAND UP and FIGHT!. Fight for those who can not, for those who won't and for those that don't know they have something to fight for....

MAN IN THE ARENA
It is not the critic who counts; not the man who points out how the strong man stumbles, or where the doer of deeds could have done them better. The credit belongs to the man who is actually in the arena, whose face is marred by dust and sweat and blood; who strives valiantly; who errs, who comes short again and again, because there is no effort without error and shortcoming; but who does actually strive to do the deeds; who knows great enthusiasms, the great devotions; who spends himself in a worthy cause; who at the best knows in the end the triumph of high achievement, and who at the worst, if he fails, at least fails while daring greatly, so that his place shall never be with those cold and timid souls who neither know victory nor defeat.


QUOTES ABOUT GIVING

I am only one, but I am one. I cannot do everything, but I can do something. And I will not let what I cannot do interfere with what I can do. ~Edward Everett Hale

Nobody made a greater mistake than he who did nothing because he could only do a little. ~Edmund Burke

Nobody can do everything, but everyone can do something. ~Author Unknown





Sunday, February 3, 2013

Hello, It's Me - February 3, 2013

Mom and Uncle Bill

February 3, 2013

It's been a while since I've posted...and so much has happened.

I think of Mom everyday and miss her so much.  All those feelings come rushing back when I do...I should have been a better daughter, she deserved so much more than she received.

So...till I'm no longer here, I will do whatever I can within my power to raise money and awareness for Cancer Research...and VHL.  Because, I made that promise.

My daughter, Shana and grandson Davonte both have VHL.  I worry everyday, that VHL will rear it's ugly head again...it's difficult knowing it's lurking there.  We are always waiting for whatever comes next.  This past year has been a good year...nothing new has popped up.  I hope it stays that way.

I don't worry for myself as much as I worry for my children.  I know it's there...I'm not afraid, I know I will have to deal with whatever it brings...but, I will worry when I have something to worry about.  That's our family motto as it concerns VHL.  We will worry when we have something to worry about...because worrying isn't going to change anything. 

My last  check...they found 3 new tumors in my right eye.  I'll be having laser surgery soon.  Then...endochronolgy. (sigh)...I'll worry when I have something to worry about.

I'm in MDR Mode now.  I just sent out the SAVE THE DATE!  Mom's Day Run 2013 will be on May 12th.  We are hoping to pass the 200 mark.  That's 200 run/walkers!  I've set up the Registration Link and updated the Facebook Page.  I will start sponsorship solicitation soon.

REGISTRATION INFO FOR MDR: http://www.active.com/running/ventura-ca/moms-day-run---2013

PHOTOS FROM MDR 2012: http://www.facebook.com/#!/events/359846527371706/.

MOM'S DAY RUN FACEBOOK PAGE: http://www.facebook.com/#!/events/359846527371706/?fref=ts

I'm currently employeed with The Leukemia & Lymphoma Society.  I work with Team in Training which is one of LLS's fundraising groups.  I've fundraised with them for several events.  And They've been really supportive with our Mom's Day Run.  Hopefully we can grow the MDR and raise even more money this year.  I think, keeping it a Home Town Event is what makes this event so appealing.

I'm also working with VHL to have our very own 5k in September, in Ann Arbor Michigan at Gallup Park.  I'm excited to be a part of this and hoping we can create a buzz...and have a TEAM VHL!!!


Gotta Run,
Suellen

Marianne's Family



Sunday, July 31, 2011

Happy Birthday Mom! ~ July 31, 2011

A year ago today, we spent your birthday together.  You were surrounded by your children, grand children and great grand children.  We never imagined that two days later you'd be gone.



July 31, 2010
  As I look at this photo...I remember.  I remember that I was concerned.  Something was wrong.  I never guessed that VHL had reared it's ugly head.  You were 71 years old and never complained of headaches or dizziness.  It was Aunt Val who mentioned...maybe???

The next day was the beginning of a horrific nightmare.  This week has been difficult for your family.  Not that we haven't been grieving for the last 363 days but because each day takes your farther and farther away.

Remember, way back when...you read a book about Edgar Cayce.  You were intrigued about his life and mission.  I later read the book and we would have discussions about life and the hereafter.  We talked about these things for hours and hours.

Last week, I went onto the ARE website, dedicated to his readings and found one regarding "Coping with the Loss of a Loved One".

It read:

Coping With the Loss of a Loved One

Doves FlyingOf all the helpful information from the Edgar Cayce philosophy, one of the most comforting is the promise that life is continuous; our time on earth is just one aspect of a soul’s journey of growth and transformation through time. Not only will we meet our loved one again beyond the veil we know as physical death, but our relationship with them will continue as well.
Cayce suggests that one of the greatest gifts we can give to someone who has passed on is to pray for them. And most importantly, to pray that they will recognize that they have moved on from earthly life, and now have the opportunity to continue their soul development in a different way. Cayce says that those we love on the other side are actually as close to us as our thoughts, and we can be most helpful to those individuals by focusing on the happy, joyful times together, and releasing – as much as we can – the sadness and grief we feel at their passing.

We went to church today.  Jeff delivered a beautiful Liturgy.  In the prayer he asked for prayers for family members who were struggling with their health.  I cried.  A woman sitting next to me laid her hand on my arm.  That touch meant so much.  Just a touch from a stranger, who doesn't know my story.  It was thoughtful and very nice.

Edgar Cayce learned that we are here on this earth to love one another.  Very simple...and today's sermon was about loving one another despite our differences. 

So today, I'll look forward...knowing you can hear me and try not to be sad.  Mom, go forward, live, love and be joyful.  I know you can see us...

I love you,  see you soon,
Suellen

EDGAR CAYCE
www.edgarcayce.org/

Friday, July 15, 2011

Kennedy's Book

I wrote a book about Kennedy asking "Where's Grandma?"   It was shortly after my mom passed away and she asked her mom, "Where's Grandma?"  It was a sweet and simple conversation by a three year old.


Kennedy, age 4, learns that her great grandmother has passed away and gone to heaven. Follow along as she deals with "grown up" emotions in her own special way.
 






You can purchase by clicking this link:

Support independent publishing: Buy this book on Lulu.

Saturday, May 14, 2011

SHANA'S SURGERY ~ 4/25/2011

Whew!
What a crazy couple of weeks.

It started...end of March.  Shana wasn't feeling very good.  Headaches, dizziness...the words that scare me the most.  She went to the doctors, then you have to wait for a referral that never comes.

On April 15th, she goes to the ER.  Thankfully Tiana (my grand daughter) goes with her....and texts us on the developments.   Then I get a call in the middle of the night...they are keeping her, there is a tumor and cysts that they need to remove.

As I hang up the phone, a dark cloud comes over me.  Remembering my mother's surgery last summer.  Dread.  Fear.  Sadness.  ...and worry for my daughter.  What she must me going through right now.  VHL Sucks!

I never get back to sleep.  I go downstairs and wait for the sun to come up.  I pack and leave for the hospital.  My husband is so very understanding, I kiss him good bye... 

Mama Bear takes over.

The drive is about 1 1/2 hours...I pick up my grand daughter and meet at my other daughter's house.  We are all nervously quiet.

Loma Linda University Medical Center is in Loma Linda, California.  San Bernardino County...about 100 miles from my home. 

We get to the hospital and Shana is worried.  She had been crying.  My heart breaks...  She tells us what the doctors have said and surgery is scheduled for Monday.  (it's Saturday).  I ask the doctors and nurses about testing for a Pheo (pheochromocytoma).  I believe this is why my mother passed away during her surgery.  The doctor orders a 24-hour urine test.

I've packed for a few days, knowing that I would stay with the kids.  It's hard being away from my husband but it would be harder not being here.  We go through the motions and prepare for Monday.

Monday comes and we don't have a definate time.  We are all waiting in the waiting room.  Shana can only have two visitors at a time.  We rotate.  Her children, her siblings, her parents...all there.

I've been asking about the test results.  No one seems to have an answer.  I tell the nurses, "I will not allow surgery to happen without those test results".

Eight hours have passed...

Finally at 6pm, the surgeons come in.  They are ready to take her to surgery.  I ask about the tests and they say they are taking her without the results.  I ask "why did you order a 24-hour urine test, if you weren't going to wait for those results" ?  I tell them, they can not do the surgery without those results.  I explain that if she is in surgery and the Pheo "fires off"...she could have a crisis on the table.  I CAN NOT LET THEM DO THE SURGERY.  The surgeons then get on the phone...later I find out they are speaking with endochronologists.  ...and they decide they need further testing.  CT Scans follow, blood tests...and we wait for the urine test.  I find out later that they had to send that test to an outside lab and it could take a few days.  I also notice the nurse running into Shana's room to get her urine out of the refrigerator.  24 hours were up at noon on Monday.  They  never had any intention on using the urine tests to decide.  UGH!

I get so frustrated with doctors sometimes.  Some listen, others placate, most ignore me.  But after experiencing my mother's surgery.  I will NEVER not ask question with out a satisfactory answer.  I only have one Shana.

This surgeon is experienced in vascular neurosurgery.  Which is a good thing.  Hemangioblastoma's are highly vascular.  But he only does surgery's on Monday and Thursday.  So we hope surgery will happen on Thursday.  

....it doesn't.  Test results are not back yet.  The CT Scan shows an abnormality on her adrenal gland though.

Waiting for surgery


Shana is getting restless...it's hard being in the hospital, away from home and your kids.  Even though we visit every day.  She wants it to be over with.

Pastor Kenny comes by...he is an awesome presence.  He is sweet, gentle and kind.  He listens and then prays with us and for Shana. There is a light in the room...I feel my mother there.

Shana's surgery is now scheduled for Monday afternoon (April 25th).  That morning, I get up with the kids...the plan is to take them to school, I will pick them up as soon as I'm given the surgery time (they can't afford to miss much school, especially so close to year end) and get to the hospital directly after.  So we get up...I walk the dog, as soon as I get inside, Tiana is at the bottom of the stairs: "they are taking mom into surgery now".  Ack!  I tell them to get up and ready, we need to leave ASAP!!  I call my other daughter, who happens to be on her way to work and right around the corner from the hospital.  I ask her to make them wait till we get there.

We're 20-30 minutes away...and it's rush hour!

When my mother had her surgery...I knew she would be having surgery but I never imagined it would be immediately.  When I got to the hospital...she was sedated and tied to the bed.  They said she was fiddling with the IV's. My mother was blind, I knew that this is the way my mother saw.  Through her fingers...she wasn't fiddling...she was looking.  She was sedated.  I hope she knew we were there.  I kissed her and told her I'd be "right there" waiting for her to come back.   ....I never saw her again.

I couldn't let this happen with Shana!  Neysi would hold them off at all costs...and she did!  She told the nurses...that they COULD NOT take Shana without her family seeing her. Trying to explain what happened with her grandmother.  She was in tears and the anesthesiologist told her they would wait.  Thank Goodness!  Because I broke speed limits to get there.  So did her father and brothers.  We all got there at the same time and were able to see Shana before her surgery.

She seemed ok with it.  She wasn't scared.  She was calm.  The anesthesiologist prayed with us.  I kissed her cheek and reminded her what grandma told her in Shana's dream.  "Everything will be ok".  Then they took her off to surgery.

My other daughter and I went to the chapel...we prayed.  I asked for God to be with her.  To guide the surgeons, to please bring her back to us...  I also asked my mother to hold her hand, cradle her in her arms and keep her safe.

The thing I really like about his hospital is they text you as surgery progresses.  So while in the waiting room, they texted when the surgery began.  When they started the incision, when they were working on the mass...and then, 5 minutes after they started on the mass...we get a text saying the surgeon wanted to speak with us.  AAAAAWKKK!  I've seen it on TV many times, but never experienced them calling us into a special room?!!!  Neysi is trying to keep me calm.  I'm starting to panic...I'm brimming over with tears.  The stress of the last 10 days, is just too much.  I've tried to stay strong for my family....

The surgeon comes in...I can barely talk but I ask him "Is she ok?"...he says "Yes".  I ask "Yes"????   My ears hear it but...I'm barely processing any verbage.  But she is ok.  The other surgeons are closing.  He said, everything went as planned.  I ask him if I can hug him...I do.  And I say: "God Bless your hands".  A relief sweeps over me...but I know I still need to be strong...recovery takes months.

We go back into the waiting room.  My grand daughter is standing at the edge of the waiting room. looking so frightened and concerned.  I tell her everything is ok.  A big sigh comes out of all of us.  We wait till she goes to recovery in ICU.  Saying our prayers and thanking God for this blessing. 

I have this thing with Shana.  I KNOW she is ok when I look into her eyes.  She knows this...no words need be spoken.  I just know.  As soon as I see her...no matter how many tubes and wires are in and around her...her eyes, tell me she is ok.  She is ok.  She is tired, weak and needs rest, so we limit the visit to just minutes.  All the other family members come and see her, two by two.  We leave her to rest...and will be back in the morning.

I feel like I've been at the "starting line" of a race for the passed 10 days.  I cry in the shower...not wanting the kids to see me crumble.  I try to be strong.  I say my prayers everyday!!

The next day Shana has already been out of bed...doing laps around the nurses station.  She only spent 12 hours in ICU.  She is so strong...she amazes me!

She gets to go home on Thursday...13 days in the hospital, 4 days after surgery. 

One evening, as I sat on the edge of her bed...she tells me, "I saw grandma", "I felt her hand on my face, brushing the hair from my eyes"...like she used to do when I was little.  "She cradled me in her arms".  Tears spill down my face.  I knew my mother would be there.  She and Shana were so very close.  There is a calm and peace about  my daughter now.  Something we've never experienced before. 

Not long after my mother passed away, Shana had a dream about my mother.  In the dream, my mother was mad. "damned VHL!"...my mother rarely cussed, if ever.  She also told my daughter that "Everything is gonna be alright".  We hold on to those words.  I reminded Shana about her dream, just before she went into surgery.  They give us all peace.


Our family at the Mom's Day Run.  Shana is in the wheel chair.

We planned a Mom's Day Run in memory of my mother and in honor of Shana.  Shana was determined to be there...and she was (13 days after surgery).  We had a good turn out despite the the previous month (I wasn't able to advertise as planned).  We raised $1,500 for VHL!!!


Shana at the Mom's Day Run ~ VHL Sucks shirts

The Start

My sister's tee-shirt
A Moment with Mom

The participants, mostly family and friends, sprinkled with a few strangers...were all so kind to come out on Mother's Day and run along the beach with us.  Some spoke to my daughter, giving praise and commenting on her remarkable spirit.  Hugs, words of inspiration and encouragement...it was a beautiful day.

After the Run, we went to the sand (we had spread my mother's ashes at sea) and had a moment with my mom.  We miss her so much...and know she is proud of us today.  We will honor her memory every day...especially Mother's Day with the Mom's Day Run, raising money and awareness for VHL in her name!

SIDE NOTE: Up until this surgery, Shana's medical team has been watching five other brain tumors.  Watching for any new development or change.  After her surgery, they did a MRI...and to our amazement, there are no other tumors in her brain.  I can't explain it... and I don't think I need to. 

Prayer works! 

We are so greatful, today! 
We know that with VHL...you have to be "on guard"...because it's always lurking there...but today, we are "thankful"...we are "greatful" to have one more day.