Archive for August, 2009

Many things

First off, the service for Michael in Tampa was great.  Is great the right word for a funeral for a  2 1 /2 year old.  Probably not.. Let me rephrase.  Rachel did a great job of making a beautiful memorial for her son.  We miss you Michael.   I have other pictures but here is one that I thought would be appropriate to share.

Elmo for Michael

Elmo for Micahel. Elmo is wearing his ribbon for Michael. It is gold (for pediatric cancer) and red for Elmo!

I have to say while I was gone I missed my kids like crazy!  I must have kissed them a million times.

Angie Natalie Mary Ann Rachel

Angie Natalie Mary Ann Rachel

**After the service we went to Clearwater Beach to have supper together.  It was nice to hang with my girls and have supper over the sunset.  ****

Taea started 4th grade on Wednesday.  So far she likes it.  I think her favorite part actually is riding the school bus. I never allowed her to ride the school bus before in St. Petersburg.  I just thought the drive on the bus was too long and too dangerous.  Well seeing as how the school is a whopping 5 mins from our house and there is a small amount of people here I figured I would let her ride it.  

My 4th grade girl!

My 4th grade girl!

 

We took the boys to the barber shop.  I have to say I think they cut Jarek’s hair a little short but he looks like a little man, don’t you think?  Where did my baby go?

Little Man

Little Man

 We are preparing to move again.  We can move in on the 1st so I have been busy trying to get ready for that also.  I had to go to Rapid today and get curtains, and baby gates.  There are 2 sets of stairs and so I had to get something to TRY and keep my little monkeys off the stairs!  We will see if that works.

That covers a couple of things right now.. I’ll update more whenever I can.. For those 2 of you who are reading.

Don’t forget to wear a GOLD ribbon in September to show your support for Pediatric Cancer!

Rest in Peace sweet angel

Today heaven received another angel.  Michael Jaden Perez went home to be with Jesus today at 7:50am est. 

He put up a long hard fight from ATRT ( a rare form of brain tumors) .  Please keep Rachel (mom) and Jade (sister) in your prayers.  They are in need to be lifted up.

Feel free to visit.  www.carepages.com   page name  (PassthePrayer)

Good Counts-Jellied out

Just a quick update… Micah’s counts were great yesterday!  I also had them run a panel to check for celiac disease and for his thyroid.  Those won’t be back for probably about a week.  I will post about those later.

I have been so busy! WOW.. I have been working (at A Step Ahead) trying to get ready to open, teaching Zumba at night, and oo did I mention.  I just canned 31 jars of choke cherry and apple jelly?  OO yeah, go ahead feel free to call me Miss Suzie Freakin’ Homemaker!

Somewhere along here I am suppose to move…hmmm,……

Bill Of Rights

SO THERE

SO THERE

BILL OF RIGHTS for parents of children with special needs

* We have the right to expect our kids to be seen for who they are as individuals, not as labels or diagnoses.
* We have a right to trust our instincts about our kids and realize that experts don’t always know best.
* We have a right to ignore the remarks, questions and stares and not give explanations or excuses for why our children are the way they are.
* We have a right to choose alternative therapies for our kids.
* We have a right to roll our eyes straight out of our heads when we encounter certain mothers who brag nonstop that their kids are the smartest students/best athletes ever.
* We have a right to wonder “What if…” every so often.
* We have a right to play aimlessly with our children. Not for therapeutic or educational purposes—just for fun.
* We have a right to blast Bruce Springsteen/Tom Petty/Any Rocker, down a glass of Pinot Grigio, get a pedicure, go out with the girls or do all of the aforementioned at once if that’s what it takes to avoid burnout.
* We have a right to react to people’s ignorance in whatever way we feel necessary.
* We have a right to not always have our child be the poster child for his/her disability and some days be just a child.
* We have a right to go through the grieving process and realize we may never quite be “over it.”
* We have the right to give our kids chores. Even better if they can learn to make breakfast in bed for us.
* We have a right to stretch the truth when we fail to do the exercises the therapist asked us to do this week because we were too darn tired or overwhelmed.
* We have a right to have yet more Pinot Grigio.
* We have a right to fire any doctor or therapist who’s negative, unsupportive or who generally says suck-y things.
* We have a right to tell family and friends that everything may not be OK—at least not how they mean it, anyway.
* We have a right to hope for an empty playground so we don’t have to look into another child’s eyes and answer the question, “What’s wrong with him?”
* We have a right to bawl on the way back from the playground, the birthday party, the mall or anyplace where our children’s challenges become glaringly obvious in the face of all the other kids doing their typical-development things.
* We have the right to give our children consequences for their behavior. They may be “special” but they can still be a royal pain in the butt.
* We have a right to take a break from Googling therapies, procedures, medicine and treatments for our kids to research upcoming concerts, exotic teas or anything not related to our children’s disabilities.
* We have a right to talk about how great our kids are when people don’t get it.
* We have the right to not always behave as inspirational icons who never complain or gripe about the sometimes awful realities of raising a child with special needs.
* We have a right to expect quality services for our children not just when they’re infants, preschoolers and elementary school age, but when they’re in older grades and adults, too.
* We have a right to adequate funding for those services and to not have to kick, scream or endure a wait for them.
* We have a right to get tired of people saying, as they give that sympathy stare, “I don’t know how you do it.”
* We have a right to wish that sometimes things could be easier.
* We have a right to cheer like crazy anytime our children amaze us—or weep like lunatics.
* We have a right to push, push and push some more to make sure our children are treated fairly by the world.

(Compiled by Ellen in honor of her little boy, Max, and all of our beautiful children, on June 17, 2009.)

 

 

*** Thanks Renee for this, it was so great I had to steal it and post it on here! *****(www.myspecialks.com)

August 11th 2009

August 11th is the day.

August 11th will be 3 mths since Micah has had blood work.

August 11th marks 3 mths that we have tried to NOT think about cancer.

August 11th will be a truth telling day.

August 11th will be nerve racking.

August 11th will be another day we need a lot of prayers.

We would appreciate a few prayers that Micah’s blood work comes back A-ok!

***Side Note***

Please pray for 2 of my dear friends.   Dawn, her son is having a major surgery on August 11th

Rachel, her son Michael has ATRT (brain tumors) that will inevitably take him home to be with Jesus, please pray for her, Jade and Michael make it though this very difficult time.  If you want to read more about Michael check out her carepage.   www.carepages.com   PAGE NAME  PassthePrayer

Movin’… again

Yeah folks you have heard it here.  We are moving again. 

I put my notice in that we can’t run the motel anymore.  We are staying here until the end of the month.  The we will be moving into a townhouse not too far from here.

The Lord has answered our prayers.  I have been praying for the decision about the motel for a while now.  The Lord has answered our prayers. 

This week is the Sturgis Rally.  So needless to say I have been pretty busy. 

It’s just the first day of the rally and the bikes are everywhere.  It’s pretty cool.  I think we are gonna go to Sturgis to see Korn on Monday night.   That should be fun.

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