Wednesday, September 24, 2008

Have you been waiting?





Hi Folks! Yes, we are still here. A lot has been happening for Griffin and family. The Maks' are busy acclimating to their jam-packed schedule. Markings on the calendar indicate the start of school for Griffin and his siblings. There are also reminders for soccer practice and games, violin lessons, Tae Kwon Do practice, and hospital visits and procedures.

Since the last posting Griffin has had treatments that follow the planned schedule. Not to say that the events that have passed are not important to note here on the blog, but Gretchen and Jon are super busy.

Griffin has been attending classes at the local park district Monday through Wednesday for two hours each time. He enjoys the playtime with his siblings and playing with the tool set play area. He especially enjoys the different art projects, playdoh playtime, and floam.





Griffin has continued his involvement with all of his therapies. Gretchen stated,
"All the outside daily stimulation/ socialization helps keep a constant state of order." Griffin and his siblings are not only learning the valuable lessons of play, but also understanding the concept of rules and continuing an established routine.

The blog has not been updated for a long while and we Thank you for being extra patient. On Thursday, September 25, Griffin will be on his 29Th day of the Standard Delayed Intensification Phase. This is the 4th phase of Griffin's treatment.

Tomorrow Gretchen and Jon will be at the hospital for Griffin's procedure. The first part of day Griffin will have to undergo yet another lumbar puncture (LP) also called a spinal tap. This LP will be done without general anesthesia. Usually this procedure with the anesthesia takes about 2 hours, but Griffin has to undergo a new chemotherapy regimen. The medication that Griffin will have to receive is called Cyclophosphamide (Cytoxan). The infusion time for this medication is planned to take 6 to 8 hours.

In addition to this medication, Griffin will also be receiving a slew of other medications. They include:

Thiogiane (sp?)via the port-a-cath.

Cytarabine via intravenously and then continue daily at home as a deep muscle injection for 5 days.

Griffin may have to stay overnight at the hospital depending on the outcome of all the procedures.

On a side note, Griffin's hair is beginning to show signs of thinning. His hair may look disheveled and unruly covering his eyes, but Gretchen and Jon are nixing the idea of giving Griffin a trim or cut. They are keeping his hair until it starts to fall out.





Gretchen and Jon are very thankful for all the e-mails, cards, and phone calls. They are also thankful for the gifts of toys, books, photo albums, and food.

The Maks Family ask for continued prayers and positive energies.

5 comments:

Jenny said...

If anyone would like to volunteer meals please contact me:

Jenny Ore
e: jen_ore@yahoo.com
c: 847-804-4777

michele said...

Stay positive... Praying for Griffin's recovery from today's procedure...

ghamer said...

I absolutely love the new photos. Griffin and all of the other siblings are just adorable. You have a very beautiful family. My entire Sunday School class prays for your family every week. And YES! there is power in prayer. God is Jehovah Rapha - The Lord who heals!!!!

Big Hugs!!!!

Love - Angel Genevieve

Unknown said...

Hi Gretchen and Jon,

I love the new pics! YOur kids are so adorable, Hudson is so handsome! Kai is so lovely, she looks very much like you Gretchen.

I am grateful to know you, you are so mabait people. I pray for Griffin and your family everyday. Keep the faith and try to live one day at a time. God is so good.

I am praying that your family and mine will meet someday.

I love you.

www.caringbridge.org/visit/elishalacson

Lourdeline
Pasig City, Philippines

Lalulove said...

Jon and Gretchen,
We Pray for your whole family everyday. God is Love , and only He knows what the plans are for you . You will be rewarded . We love you , God loves you very much .
Tito Tim & Tita Marylou