Showing posts with label Leukemia. Show all posts
Showing posts with label Leukemia. Show all posts

Thursday, September 23, 2010

Will You Join The Fight?




2 More Days left until the LIGHT The NIGHT

Will you be joining us?

Come on out tonight for yummy food, great people, and good times.

TEAM GRIFFIN'S KICK OFF PARTY

Thursday September 23, 2010

HOULIHAN'S RESTAURANT
550 W. Touhy
Park Ridge, IL
847.692.6505

6PM-9PM


There will be free appetizers for our bunch

20% of dinner receipts will be donated to TEAM GRIFFIN

Fundraising continues with T-Shirt sales...get them while they are hot!

Come on out and meet GODZILLA he is hungry for your donations.

Raffle prizes a plenty.

Catch Griffin and his family here and the first round of Root Beer is on me!

Make a donation and find Godzilla at the event or link to TEAM GRIFFIN



(GODZILLA creation c/o Wayne Rizal-president CALAMBA ASSOCIATION of ILLINOIS)




The Maks family house is brimming with last minute details for the walk coming up this Saturday. Gretchen and Jon continue their efforts to raise funds for the walk as well as quell any tantrums inevitable among the Maks siblings.

Last night Griffin busy playing hide-n-seek with his cousins and made out to be a very good hider and seeker.

Want to find out more about this little dude?

Meet him tonight and JOIN the Fight!

See you there!

Monday, September 13, 2010

2010 Light the Night Walk *Team Griffin*

I remember the day when I was a kid playing endlessly at the park, climbing the monkey bars, spinning in the tire swing, and jumping on the teeter-totter. I played until the park lights started to flicker on and the setting sun cast it's last rays.







Over the weekend, Griffin (my 4 year old nephew), took a break from playing in the park to capture a few smiling images. We had walked a few steps around the jungle gym to find a spot for him to show off his cheeky smile and he said to me,

"I can't walk far because my legs hurt."

I proceeded to find out more about the discomfort that afflicted Griffin, and asked him my cadre of questions to find cause for his pain. Griffin answered my what, where, when, why, and how framework of questions. Griffin described his legs were hurting because he was playing in the park. He confirmed that he did not get bumped at the playground by his rambunctious siblings-Everest, Hudson, nor Kailey. He did not fall off the jungle gym, and he had not been play fighting Tai kwon do with his cousins (my rambunctious kids). Later on, my sister, Gretchen, told me the chemotherapy medication Griffin received made him tired and caused pain to his legs. Griffin left the park not too long after the images were taken and just prior to the debut of the evening sky making it's appearance.



I did not understand Griffin's pain because growing up as a kid I did not have the same experiences that Griffin has to endure. I have stopped asking myself the why about Griffin's Leukemia and find myself asking what can be done.
"What can I do to help my nephew not experience the physical pains after performing activities that children inevitably do growing up?"



On Saturday, September 25, 2010, Griffin and his family plan to attend The Leukemia & Lymphoma Society's (LLS's) Light the Night Walk.





Joining TEAM GRIFFIN will be family and friends helping to raise funds for lifesaving cancer research. I join the fight to find a cure for Leukemia. A disease, in my opinion, that steals away the fundamental right of growing up as a child. I invite you to join Griffin.



Special mention who have and are still helping Griffin Maks and his family, including the Elizabeth Meyer School --Griffin's preschool. On behalf of Gretchen and Jon Maks: A huge Thank You for your efforts. We look forward to a good turnout in support of leukemia research!






Saturday, July 24, 2010

Rah*Rah*Sis*Boom*Bah



Whether I cheer on the sidelines with pom poms in hand, or I scream and shout from the bleachers, I am showing my support for my team. I know that I can be overzealous shouting out my encouragement to the players on the court. I may stamp my feet and clap my hands. I have been known to stand up from my seat and call out to the referee. I do this to channel the energy that I have, to both inspire and maybe even give that extra "edge" to the players so that a victory will be won. I am preparing to watch my son's basketball game tomorrow morning. My son and my nephew (Everest) play basketball together. Everest is Griffin's older brother.

I plan to cheer for the basketball players tomorrow as I do for my nephew, Griffin. I cheer for Griffin everyday. My cheers for Griffin ride along with my thoughts and beliefs of my faith. I pray to God to keep Griffin well, healthy, and happy. There are other participants on the field who also deserve encouragement. These first string players need no introduction from me. You know them by a first name basis. Jon, Gretchen, Everest, Kailey, and Hudson.



The playing field is set in a number of different places. The fourth floor clinic at Children's Memorial, the house at 60076, and even the car ride to the emergency room. I am shouting out encouragement to

"...keep cool, relax, continue to do what you are doing..."

I am encouraging the players to endure, to sacrifice, and to overcome what may seem to be the hardest hurdle yet to be faced.




The current situation sets the players at different places. Everest is with me for a very early game in the morning. Hudson and Kailey are snug in their bed with grand-parental supervision. Jon, Gretchen, and Griffin are on the way to Children's Memorial. Griffin's white blood cell count has been trending on a downward slope. This situation challenges Griffin's body and makes it hard to fight off infections. Griffin had been monitored by the Md's for the past week plus a few days. Gretchen and Jon were given instruction to come to the hospital if Griffin developed a fever.
I had talked to Gretchen over the phone on Saturday evening (I can not change the time entered/displayed for this post). She spoke to me with tears and told me her "mother's instinct" and interpreted her gut feelings. She was preparing and packing in case Griffin did indeed show more objective signs of fever. I received the call Saturday night (before midnight) they were in fact on their way to the hospital.

Griffin has one more year of treatment and must face every challenge with strength courage, and faith. As I sit here in front of my monitor I invite you, reader, to join me on the sidelines and Cheer your heart out for the Home team. We can do a virtual wave, we can whirl a dervish dance, we can scream from the rooftops, we can send our positive energies, we can pray. However you choose to cheer, encourage, uplift and/or inspire...let us all tip the scale in Griffin's favor. 1-0.