Our portion of MRI -- a few hundred dollars
Parking fees at 2 different facilities -- $14
Co-pays for 3 different docs -- $90
Finding out your kid will be fine -- priceless
So Chip has been having some issues w/ his eyes. If you know much about brain tumors, you know that eye symptoms freak out parents of BT kids. I was fairly sure that Chip's problems were just w/ his eyes, but it was still hard not to worry.
Long story short, we headed to ATL this week for an MRI, to see Dr. Claire, and to see a neuro-opthamologist. The MRI was normal (thank you, thank you, thank you). After learning that, we headed to Piedmont to see the neuro-opthamologist. She agreed w/ us that he was definitely struggling w/ his vision, but she wasn't sure exactly what was going on. She was great and very thoughtful and called a friend of hers, a peds opth. at Scottish Rite. He was very kind and agreed to work us in that day. We met him and he quickly assessed Chip, put some drops in his eyes and said he'd be right back to let us know what was going on. We were surprised at his quick assessment and the impression he already knew what was going on (we'd already seen a doc here locally who was stumped as well). He stepped out for a couple of minutes. Upon coming back in, he looked in Chip's eyes briefly again and then sat back and told us that Chip was going to be fine. He said he has ocular motor apraxia. Basically, he can't track objects with his eyes. While we wish his eyes worked perfectly, this is SO TOTALLY something that we can handle! The problem will improve as he gets older and we are investigating occupational and/or vision therapies.
We are doing well (esp. now!!) and things continue to clip along at a quick pace. The kids are growing, are doing well at the sitter's while I'm teaching, and are, as always, keeping us on our toes!! We love the normalcy that has invaded our lives and we are grateful for it each and every day.
Please pray for our friends, the Maxeys. Their 1st daughter, Maddy, and Catie were in treatment together. They lost Maddy shortly after her 1st birthday. They are now facing extremely tough times w/ their 3rd child (2nd daughter). Please pray for Kirk, Natalie, and big brother Grant, as they take sweet Annette home. www.maxeyweb.com
Sunday, August 23, 2009
A Good Day
Posted by Jenny at 12:50 PM 6 comments Links to this post
Labels: Chip, prayer requests
Wednesday, July 29, 2009
Wow, It's Been a While!
I cannot believe it's been so long since I've written here! Blame it partly on FaceBook and partly on a really busy summer!
We have had an absolutely AMAZING summer!! The beach, the lake, the beach, the local waterpark... lazy days, busy days... Cousins' Camp, the sprinkler, Bible School. It's just been great! I love the laidback feeling and the later nights w/ kiddos. The no rush to bed and the hang in your pjs after you wake up. We have lots of pics and I'l try to get some up soon. I plan to be better about writing here, b/c I really want to record all the stuff Izzy and Chip are up to, so that I remember it and that they get to hear about.
So... that's it for now. Summer's done and the "real world" has arrived. We've got to be up and at em early in the morning. But... here's to more consistent writing!!
Posted by Jenny at 9:49 PM 4 comments Links to this post
Labels: summer
Thursday, June 18, 2009
Normal
Today was a really great day! A really great, normal, summer day. Chip went to hang out w/ GaGa and Poppy and Iz and I met up w/ some friends and headed to a nearby waterpark. It's a great spot for kids w/ lots of stuff on the sprayground and slides just their size. I loved watching the look of sheer terror on her face as she flew down the slide, and then hearing her beg, "do it again Momma, do it again!" as soon as I pulled her up from the water. She is definitely going to be more of a thrill-seeker than her momma!!
This may sound strange, but there are still times when "normal life" stops me in my tracks. It does not feel "normal" to me yet. I've been a mom for nearly 7 years, but much of that time I haven't been a "normal" mom. Catie was sick for so much of her life and the "rules" we had to play by were so different from those of normal kids. There weren't lots of playdates w/ big groups, long days at the waterpark (she had a hard time w/ heat and most of the time couldn't have made it all day), we weren't able to attend church regularly, she didn't get to go to VBS. All that is OK! We made good w/ what we COULD do and I know she lived full and happy and well... And so, now, w/ Izzy and Chip as we join in on some playdates, spend a huge chunk of the day running through the sprayground and swooshing down waterslides, attending church more regularly, and getting ready for VBS next week... as we live. normal. life. I'm simply shocked and grateful at how wonderful it is. Perfect? Nope, never is... but pretty dad-blamed good!
If I let it, it could make me sad for the things Catie missed... but I also know that she was, at least I think she was, satisfied w/ the pace of our life and the day to day way we lived. I watch little girls who are the age she would be now and I am amazed at how grown she would be. Strangely, being around girls that age is usually a comfort to me... It's the events that get me and that's completely the opposite of how I thought it would be. I confess to being incredibly sad on the last day of school b/c she would have finished kindergarten and gotten her first real taste of summer break after a full year of schedules and routines... and there were tears when she missed what I know would have been her first spend the night party... I guess it's always going to be those "firsts" that get me.... all those "normal" things she would have done. Thankfully they don't come as often as they did that first year.
So, this weekend we will honor her life and try to raise a little more money for research so that kids like her get the chance to try on "normal" life...
Oh sweet girl, I miss ya tonight. You would have loved standing at the bottom of the slide and watching Iz's face as she flew down and you would have cracked up at you brother tasting his peas tonight. I do wonder where you would fit in the mix if you were here... would you be Queen Bee, keeping tabs on everybody (it's a big job w/ that sister of yours) or would you kind of be off doing your own thing and letting the little ones be? I tend to think you'd want to be in charge, but who knows... I DO know that you are now filled w/ far more joy than any of us can even begin to imagine.
Dad and Iz are off on the golf cart making a trash run. I'm hoping they bring a few blueberries back. Izzy loves them as much as you did... she's starting to ask about you from time to time. I like that. It's hard for her to understand where you are though. That will come with time and I'm grateful for the chance to tell her Catie stories. I think I'm going to go relax and curl up w/ the new book I'm reading. Love you sweet girl... Eskimo, butterfly, Daddy, and NikNik kisses to you.
Posted by Jenny at 8:35 PM 6 comments Links to this post
Labels: family, grateful, learning from loss, Midget, Parenting, summer
Thursday, June 4, 2009
Catie's CURE Classic benefitting CURE Childhood Cancer

We're gearing up for our golf tournament for this year and it's coming up quickly. We've taken a couple of years off, but we're back and we're hoping to have a great turnout for the tourney. The tournament will be held on June 20 at Black Creek Golf Club. For details on the tourney, go to http://catiescureclassic.com. This is the first year the tournament will be a memorial tournament, but we do this to honor our sweet Catie and the life she lived. We also do it so that other families won't know the devastating loss that is so often caused by childhood cancer. All proceeds will go directly to CURE Childhood Cancer (http://www.curechildhoodcancer.org/). We are in need of sponsors (levels are: Hole for $100 and Corporate for $500 and $1000), golfers, and door prizes. Each sponsorship comes w/ different perks, so visit our website to check them out (http://catiescureclassic.com/).
Given the lovely economic times we're in, we're taking a bit of a different approach this year. We are still seeking "normal" sponsors (at the levels listed above), but we also realize that smaller donations add up to make big donations. We are seeking folks who might not be able to be a hole sponsor, but could handle giving $25 (or $10 or $50). If we could have 100 people donate $25, that would be $2500 (and the equivalent of 25 hole sponsors)... 200 folks giving $25 would give us $5000, and so forth.
So, here is my challenge to you. (I'm not usually one to issue challenges, but today I'm going for it). If you are able and willing to donate to our cause, please do. You can easily do it through PayPal on our site (http://catiescureclassic.com/) or to Catie's Fund page ( http://www.curechildhoodcancer.org/default.asp?contentID=66). If you donate at Catie's Fund page, please list "Catie's Fund for Golf Tournament" in the comments section. The second part of my challenge is this... PLEASE forward this on to folks on your contact list. If half of the folks who receive this e-mail give a small amount of money and if everyone forwards this on, we could really build a large army and raise a lot of money.
Forwarding is a HUGE part of this effort because it allows us to reach a large number of people.
Thanks for taking the time to read this and thanks for forwarding this on and donating if you are able. These donations (which need to be made by June 26) fund research that is literally life-giving.
Posted by Jenny at 12:13 PM 0 comments Links to this post
Labels: Charities, events, Midget, Research Funding
Tuesday, June 2, 2009
Conversations
This morning at breakfast, Izzy was eating the first blueberries and blackberries from our yard this year when out of the blue, she looked at me and asked, "Momma, Catie like blueberries?" It's the first time she's ever asked me about something Catie liked or didn't like. I told her that yes, Catie liked blueberries (and strawberries) a lot, kind of like she did. Then she pointed to her bowl of cereal, "Catie like cereal, Momma?" And I told her that yes, Catie liked cereal, but she liked it dry in a cup, not w/ milk in a bowl like she did. She seemed satisfied, and I appreciated that she had asked, so we went on with our morning. A little later, as we were riding in the car, she said, "Momma, I want to go to Catie's house." In my mind, I was thinking, "me too baby, me too." But, out loud I said, "Well, Iz, who does Catie live with?" "Jesus." "And where does Catie live?" "In Heaven." So I told her about how Heaven is way up high in the sky above the clouds and that loving Jesus means we go to live there when we die. I told her that Catie was little when she died, so she's gone there before us. And I told her that we would go to see her sister later when it was our time to go to Heaven. Again she said, "I wanna go to Catie's house." So we talked a bit more... Time and space and living and dying are hard enough to understand when you're grown, much less when you are two. But I confess to loving that she's opening the door for conversations about Catie and about Heaven.
I worry that she will be scared of dying b/c Catie died young. Today was the first time I've used the word "die" with her and a couple of weeks ago I used the word "cancer" w/ her for the first time(the child life folks say to be sure to call diseases by their real names and to not say, "Catie was sick and she died" b/c then they'll be scared the next time they get sick.) I wish she didn't have to know that kids could die. I pray that God will give Tre' and I wisdom to guide her (and Chip) in all things, esp. important stuff like we talked about today. I sure do wish I could see in her mind to see how she's making sense of things.
Posted by Jenny at 4:15 PM 3 comments Links to this post
Labels: hope, learning from loss, memories, Midget, Moonpie, Parenting, toddlers
Sunday, May 17, 2009
Living Gratefully
In college, my roommate and I had a book called 10,000 Things to be Happy About. It was a smallish, but chunky book that simply listed things that the author was grateful for... things that made her happy. For a while, Alice and I would take turns reading through the book and highlighting the things that made us happy as well... Then we started our own "Happy Journal." I still have it and on occasion (though it's been far, far, far too long) whoever has it will pull it out, write in it and then mail it to the other one. I don't think that I've written in it since Catie died, not because I'm not grateful, but b/c sometimes I think some of the things I'm thankful for might sound strange once I write them down... For instance, how can you be happy about a melancholy evening b/c it makes you feel closer to the daughter you've lost?
But the other night I walked out of CVS w/ Chip snuggled against me (there's something for the pages of our book) and the mugginess of the air hit me... it was the first breath of a hot summer night I've felt this year... and honestly, the first time I really remember noticing it since she died. I know I've felt it, but I haven't noticed it. That muggy breath of air took me back to bike-riding down a hill like I did many a night in the neighborhood I grew up in... and playing kick the can at my Granny's house w/ the other kids in the neighborhood... nights at the ballpark...
It's strange how I'm suddenly able to notice more things in recent months... things that I've experienced in the last 2 years, but have somehow missed. I still miss Catie, in fact, I've really missed her even more the last couple of weeks... but somehow, some of the fog seems to be lifting a bit. A fog that I don't even know that I knew was there.
I think I might have to take to writing in that old journal again, even if some of the things I write seem a little odd.
Posted by Jenny at 9:29 PM 3 comments Links to this post
Labels: family, grateful, hope, learning from loss
Saturday, May 16, 2009
And Because I Can Never Ge Tired of This...
Posted by Jenny at 11:03 PM 3 comments Links to this post