Monday, July 28, 2014

Soccer Week

Toe and "Little Wheels"
 LCYSA does an amazing soccer camp. Toe had such a great time. Three hours a day for four days (the camp runs five, but we pulled Toe Thursday and rested - he was exhausted!) Toe played games, learned skills, and ran, ran, ran. All of the younger kids warmed up together playing games led by the camp leader, Wheels (all of the counselors had camp names), and then the kids were divided into small groups. The smaller sessions had a balance of learning specific skills in a very structured environment and then had time to play games where they could get in in play right away.

Wednesday's water day was a great way to hit the middle of the week. The kids were having fun, but they were tired. The last 45 minutes, the counselors talked about expectations (outlining the dry zone, talking about safe practices with each other and the sprinklers),  handed out squeeze water bottles, filled with water, and let the kids run and squirt each other. The sprinklers came on as the kids ran out of water and everyone scrambled to either get more wet or to refill their bottles. It was chaos, and the kids had SO MUCH FUN.


A safe view from the "dry zone."

The camp was run by one family. "Camp Mom" had done all of the administrative prep and was on-hand to provide ice packs, snacks, and generally help campers who needed something. "Big Wheels" (the Dad) ran the camp for older kids. "Wheels," (eldest son - finishing college) ran the camp for the younger kids and "Little Wheels" and "Training Wheels" (sons in high school) worked as counselors for the younger kids. SUCH a nice family. They definitely provided the leadership for the rest of the counselors. For a one week session, I was surprised how well they learned the campers' names and personalities. They were all excellent with Toe. The other counselors were great, too, supportive and fun, but all of The Wheels really stood out.

Just about every photo I took of Toe includes a giant smile. He did it all with a smile. And when he checked out and just started spinning or wandered off, he was gently brought back to the task at hand. It was positive, relaxed environment that was perfect for day camp. Toe is already ready for next year.




A friend of Toe's from preschool also took the camp. They had some good times together.

Tuesday, July 15, 2014

Soccer Mom

 It's official. I'm a soccer mom. At least for this week. We have signed Toe up for a week of soccer camp - three hours a day, five days in one week. Because of Toe's CF we had some concerns. We had to make sure that if another child there had CF, he/she was not placed on Toe's team. Toe has a tendency to overheat and dehydration and loss of sodium are two things that are critical issues for people with CF. He also must be given enzymes if he is fed a snack....

I think about those parents who sign their kids up and just show up, drop them off, and leave. So different from our experience. I have to call ahead and clear Toe's attendance, briefly explain cystic fibrosis, describe my concerns, fill out more detailed medical forms including doctors and insurance numbers, identify ourselves at the actual day camp... the list goes on. Everyone has been incredibly understanding and willing to accommodate Toe's needs.

We also try to make it as easy as possible. Either J or I plan to stay at each day camp to feed Toe his enzymes when they have snack, to make sure he gets hydrated, and to watch for overheating. The counselors are great, but each one is responsible for about 8 kids. I can't expect in the course of a week for them to be able to recognize how Toe looks when he overheats.
 Fortunately we live on the coast, so hot weather is unusual. Day one was overcast and 65. Today was still under 70 and sunny. Somewhere in hour two, the kids came in for a drink break and Toe had the telltale signs: flushed cheeks, sweat, slightly glazed eyes. I made him drink and pulled him into the shade with me until he cooled down, then sent him back onto the field for the last twenty minutes of the day. At that point I realized that it would be a good idea for me to continue to be there just to make sure.

The time and energy we put into it as CF parents is completely worth it. Exercise is very important for CF patients as it helps build strong muscles and healthy lungs. And running is supposed to be the best.

The camp is well run - great camp counselors, age appropriate games and drills, a flexible and fun attitude. Today was mismatch/tye-dye day (thus the backwards shirt on the counselor below). Tomorrow is water day. Standing water can also be problematic for kids with CF. We'll see how it goes. I expect to be pretty flexible and shower him afterwards. At least it will keep him cool.

Toe's joy as he plays is palpable.


Sunday, July 13, 2014

Awesome

 
For those of you who don't know, Jason's brother is living with us for a few months before he sets off on some travels. Having grown up in a three parent household, I see this as a very natural thing (My mom, dad, and grandmother all moved in together when I was one, not of necessity, but because we spent so much time together, it seemed a waste to have two houses.). 

Scott (self-proclaimed "Uncle Awesome" - an apt title) makes a wonderful and easy addition to our household.

Three years ago, when Uncle Awesome  returned from over a decade in South Korea, he needed a place to stay and moved in with us for about six months. We had a blast. Toe had a wonderful playmate. Awesome provides a different parent energy than either J or I can offer. He also is the best housemate ever - he shares in most of the domestic tasks and is an amazing cook. He is J's brother, but he his my friend as well - someone with whom I just enjoy spending time. He and J and I have all known each other since we were kids and have grown up together, so there is a real camaraderie/ family feel to the house. 

In similar fashion, he has adopted my family (especially the nieces) as his own.
 



The re-adjustment to having him live with us again took me under three days. I'm having such a good time talking about recipes and food, possibilities for the new house, ideas, plans. And I know first-hand how incredibly magical it can be for kids to live with another family member. This bond that Awesome and Toe are creating will last Toe's entire life. Awesome's plan is to stay through early fall and I am already feeling that it will not be long enough...
Today's lunch: stuffed tomatoes over eggs and hash a la Awesome.


Wednesday, April 23, 2014

Spring Surprises

 Whoever lived here previously was a savvy gardener - or perhaps there was a series of savvy gardeners here. This property just keeps amazing us. In the winter, it looked like a pretty plain yard; as spring marches through, we keep being surprised by pops of color, blooming flowers, visual delights in every corner.

We have an "orchard" with four fruit trees and, presumably, a lilac tree...


Under our laurel hedge/tree we have these: 





And this: Wisteria?? grows nearby

 The front has lithodora, heather, salal, and I don't know what else....




Like the rest of the house, it does not photograph well as a whole, but the experience is amazing. I can tell already that it has been planted with early, middle, and late blooming plants, so we will enjoy new surprises throughout the year... 

And we have just discovered that a surplus of cherry/plum/apple blossoms can, indeed, clog your gutters. Amazing.

Saturday, April 12, 2014

Art Outside

 We are also encouraging Toe to try some art outdoors while I work on the yard/ in the garden. Hopefully this will involve drawing and painting, but we started with photography.  While I mowed the lawn, I gave Toe the camera and let him shoot around the yard. These photos are all his. As a six year old, he especially loves taking photos of people's bottoms. I have spared you those.




Toby vs. the Yard


We are working to figure out ways that Toe can help in the yard without "gardening." I still need to talk to our nurse at OHSU, but I am pretty sure that the things we need to avoid are contact with soil (digging and weeding) and standing water (watering, water features). Ben said Toe could mow the lawn and pick cherries, apples, and some veggies (although I'd guess pulling carrots is out)..

So far we have tried mowing, pruning, and clipping. Toe love shears and was a *great* help cutting back one of our trees and then cutting the branches into pieces. Fortunately we have some unwanted bamboo in the back that will keep him busy for summers to come (bamboo is pretty invasive and keeps coming back, quickly). 


Toe and the saw

A different angle shows that Mom is a little cautious....
 The lawn is a triple challenge. Pushing a mower is difficult when you are four feet tall. Getting used to a mower with a cord is also trick. In addition, our lawn is sloped and very uneven. There are lots of pits to navigate and/or muscle through, made even more difficult by the angle at which you push the mower. However, Toe is game. We have a deal. He mows as much as he wants, and then I will  do the rest.


 This makes for much hilarity. I try not to laugh as he works, because he is so determined and wants this so badly. Sometimes we mow together, which means he holds down the button that keeps the mower on and I mow one-handed. Have I mentioned that my arms are getting quite a work out?

We will see how the spring develops....

Thursday, April 3, 2014

CF Update

Doctor Toe asks his father, "How do you feel?"
Some visits to the CF clinic are easier than others. Sometimes we go and they take the necessary measurements, ask us how we are, take a throat culture, and send us home. Sometimes we go and discover that Toe is sick and we need to add yet another medicine or protocol to the treatment regime. Some fall somewhere in between - they are not necessarily bad visits, but some piece of information or part of the experience catches us off-guard and we leave the place feeling slightly nauseous.

Our March clinic (early March) was one of those in-between visits. Let me say first, Toe's sputum culture came back negative for Pseudomonas aeruginosa a week later and we are incredibly grateful we were able to get rid of it, even temporarily. But that was later. This was the clinic.

New protocols for bacteria cross-contamination among those with CF now mean that Toe will have to get a mask when he enters the building and leave it on everywhere except in the exam room. No biggie. They also have new recommendations for households. We will be told details later, but the big two were 1) NO hot tubs (which we knew) and 2) NO gardening. The second one came as a shock to us. Toe burst into tears when they told us.

Let me back up a minute to explain our situation: We live in a rural area in a small town. Until this year we have rented houses, but Toe's entire life we have planted tomatoes and peas in pots in the spring. It is incredibly important to us as a family to have outdoor experiences and we have always believed that starts with your own yard. Toe has regularly helped with weeding and been allowed to dig in the dirt in the big pots where we planted tomatoes in the off seasons. We have avoided standing water because of P. aeruginosa and we have known it grows in the dirt, but we believed that if it were a true problem, the doctors would let us know. We just bought a house and were planning on growing many vegetables together in the back yard... We're not huge gardeners, but we had big aspirations.

So, back to the clinic --- Ben (our nurse) says, ".... so no hot tubs, and no gardening." Toe bursts into tears. Ben looks shocked. Toe sobs, "I was just pulling ivy yesterday!!!!" (which is true). Ben turns to his intern and says, "I hate this sometimes, having to tell families things like this." Ben tries to assuage Toe by telling him he can do some yard work - he can mow the lawn, he can pick apples from the trees in our back yard. We get the kid calmed down. But the damage has been done. A huge chunk of our lives has just fallen away. I don't know how to explain this. In the scheme of things, this is little, but to us at the time, it felt catastrophic.

Toe's height/weight ratio is also down. He is still growing. Like a weed. A skinny weed. Too tall and not fat enough. He has genetics to thank for that.

The doctor also discovers "trace clubbing" on Toe's fingers. People with CF sometimes get clubbed fingers and toes, but we have not noticed anything with Toe. It is only a slight swelling around his cuticles, but noteworthy as it can indicate lung inflammation. The doctor had Toe get a chest X-ray (this happens once a year and it was time). Toe's X ray went smoothly and the results are that things are pretty similar to last year's X-ray. There is some mild airway thickening .

Overall, it was a fine visit. Toe's chronic cough has gone away. He was cheerful and even took the throat culture with no tears. But we left feeling unhappy... a strange discombobulation. My kid can't garden with me. His height/weight ratio is off again. He has beginning indications that CF is affecting his body... None of this should have been surprising; but I have been unable to write about it until now.... Yeah. That's all I really have to say about that.