Take ’em a Meal

I’ve said it before and I’ll say it again, one of the most difficult things in this whole cancer journey has been learning to be a recipient of people’s generosity. It’s just hard to feel like a sucker–like someone who is just sucking the life of those around you. It’s hard to be humble enough to willingly receive a gift with a simple “thank you”. Very very difficult.

And yet it’s a beautiful journey to be invited into. It’s a journey that I think all of us need to be invited into from different avenues. What I mean is that some of us do not find the challenge in being a grateful recipient because we’ve been in that role for most of our lives and therefore play it well. Some of us need to learn a posture of thankfulness ’cause we’ve gotten used to the receiving. Others need to learn the posture of thankfully receiving because we’ve taken a posture of authority our whole lives. We’ve often even mistakenly placed ourselves as the rider on the white horse who comes to rescue those three feet below us. Some of us are just prideful. Some of us are just lazy. Some of us are both. And I’m sure there’s one or two of you who are neither.

This week, as we’ve been movin’ rooms around, we had many people offer to help. It was wonderfully overwhelming. In the end it was easier to have just one or two people come to do the work, but it was yet another example of our greater community stepping up in a time of need. Thank you.

The tension that it creates, however, is that there is a line. There is a very blurry and often wandering line that Jess and I are always trying to be aware of. The line has very little to do with you and very much to do with our own emotional and mental health. Because there are times that we might need help but we just don’t want it. We don’t want to always feel like we MUST have helped to survive. We don’t always want to feel like our home is overrun with people (a stark change from how we felt before I was sick to be perfectly honest). We don’t always want help…even when we may need it. Sometimes we just want to be a family. Sometimes we want to pretend like we’re normal, like our life isn’t overrun by the cancer narrative. Sometimes we just don’t want to receive.

And the reality, I think, is that those impulses are not bad. They’re not off. They’re not ‘wrong’ (though I hesitate to use that sticky word). It’s a valuable tension to hold, one that, again, is blurry in its definition but important in its usage. It’s very very important that we, at times, create those boundaries and allow both openness to receiving and protection from it to be a part of our story.

So to Blur the Lines a Bit…

I’m asking for a bit of help here. One of the things that has been hugely helpful has been the occasional meals that people have dropped by for our family. They’ve been a non-intrusive way for people to care for us, it provides a huge relief for us amidst the stress of life, and amidst the time crunch of doctors visits that run up until 5pm often days. Here’s what our friend Sherilee, who is graciously managing all of this, briefly said:

For those of you that know and love Ryan and Jessica Woods…here is a organized way to sign up to bring food. To give them time together and not worry about what to make for supper – a small gift that means so much.

She says “supper” because she’s Canadian–and we forgive her for that–but it is a small way that you can bless our family from near or far away (they’ve suggested that you can order food to have it delivered or creative things of that nature). It’s all online so it’s amazingly easier than ever before! Thank you so much for your participation in caring for our family during this really strange and surprising time of sickness. I hope and pray that one day we look back on this time and see how it was shaping us for a future life together. But if the story is different–if the story continues on the same path that it’s gone thus far then we are especially grateful for every moment that you help to create for us to be together as a family and for me to pursue a path of health as much as is humanly possible in this life.

peace.

Here’s the link to take a meal.

How to Help

I have been getting so many kind and sweet emails, Facebook messages, and texts asking how you can help. First off…thank you thank you thank you! Thank you for how you’ve already helped get us thus far, thank you for your willingness to both offer help and many of you who have not offered because your worried about trying to give us adequate space–both are a gift! As I keep saying over and over again: you all are amazing and we would not have the courage to move forward if it were not for the cloud of beautiful people that surround us.

I’m not speaking in hyperbole here when I say that receiving help has been the second hardest part only behind finding out I had cancer. I love helping people but I do not love being helped. I feel vulnerable and…well…helpless. And I don’t like that. So this post is difficult to write, but I know its important. For the sake of my wife, my kids, and myself I realize that I need to write this blog. Letting y’all help our family has been one of the most transformational experiences in my life (again, no hyperbole here) and I’m working hard on not letting my pride ruin it!

So after racking my brain for a bit here, if you’d like to be a part of helping our family, at this point in time here is how I best know you can do that:

  • Meals. I did not think that having meals brought to our house would be as big of a deal as it has been. But its been huge! By the time we get to dinner all of us are exhausted, stressed, and on edge so to have a meal prepared is an amazing gift. If you’d like to help, our wonderful friend Erika Albright has volunteered to coordinate this. Go through her ’cause she makes everything easier and keeps my clouded brain from messing up all the scheduling! Find her on my facebook friends (http://www.facebook.com/#!/profile.php?id=688805708) or email her at: ealbright2k3 AT gmail DOT com
  • Texting. For the last two months we’ve been flying by the seat of our pants. We don’t very well know what we’re doing tomorrow or what we’ll be up for doing the day after that. Because of this iIt’s been the little surprise and random things that have brought some great joys. We’ve found that some of the greatest and most subtle gifts are from those who randomly text things like “can I grab you a coffee right now” or “can we get you anything tonight” or “do you want us to stop by at all today”. Text messages like this allow us to easily say “No, we’re good” or ” No, we want to just be alone right now” OR “yes, please, we’re dying for Krispe Kreme!” or “Please come play with my children before I kill them.” We don’t do scheduling well these days, but we do SOS texting quite effectively. (if you do not have my number and want it, email or facebook me. ryan@renovatus.com)
  • Finances. I have to be honest and say that we have absolutely no idea what lies ahead for us financially. There’s obviously going to be mounds of medical bills–but even beyond that we have two difficult realities that we’re working with. First off Jess is not working right now both because her job as a teacher limits Summer job opportunities and because of the nature of what we’re going through she does not really have time to work! Secondly, my job, my role, my calling is in starting a new Jesus movement here in the downtown Vancouver community. The Grassroots Conspiracy (as we’re calling it) is just taking root…and yet I do not know what lies ahead for me and therefore for my leadership of this movement. Financially speaking it was at this exact moment right now that I had been planning on solidifying Grassroots Conspiracy’s financial future through continued fundraising and possibly a part time job on Main Street…and now all this. We are beginning dialog with some respected people trying to figure out what all this looks like, but until then, and in response to people’s question regarding financial need–here are ways you can help financially:
    • Come to the July 14th fund raiser hosted at Pop Culture! It should be a blast and I think they’ve got some great music and stuff planned. It’s from 7-9 and all ages are welcome! (you can find its facebook page titled “Fundraiser for Ryan Woods!”)
    • Online gifts. Due to my role as a church planter (another way of saying we’re starting a Jesus movement) we’re able to receive both special gifts and reoccurring gifts through this website. It safe, secure, and fairly simple. http://su.pr/1VwRyQ Again, while we’re uncertain what, how, or if we should continue the fund raising process for our work, if you would like to be a part of getting us through this, this is one easy way.
    • Snail Mail. Similar to above, if you would like to send a check to help our family with medical expenses or whatever you can do so by sending PO Box 873575 Vancouver, WA 98687 written to “Renovatus” and marked for Ryan Woods.
    • Columbia Credit Union. Our local bank was kind enough to offer to setup a donation account. If you live in the ‘Couve and it is easier, you can go into any Columbia Credit Union and say my name or give them this number #444289 and donate directly into the setup account.
  • Garden. This one may seem a little out of left field…but I love my garden…and yet I’m kind of helpless to take care of it as I should! I tried and succeeded one day in watering my front and back garden areas only to realize that it about killed my body for the rest of the day. If you ever want to help water my garden in the morning, or help tie up my growing sugar snap peas, etc. I’d love the help! The best way would be the texting approach, to drop a text offering to come over and water would be easy and would allow me to say “yes please!” or “No, my mom is here and is taking care of it”…now if we could only get some sun up here in the NW!
  • So much more. I realize there is so much more I could write. I have tried to focus on the immediate practical needs–but at this point much of my time is spent in prayer, in research, in learning about clinical trials, in learning about what resources are available to us a part of the spinal cancer family, etc. Many of you are praying, many of you have shared information regarding research, and many of you know resources. I know there are many ways here that y’all can help and I’m wide open to receive it.

Thank you all for your love, your care, your support, and your prayer. You are making love more and more tangible in my life and I cannot say thank you enough.