It was a long ride to Buckley’s Mountainside Canoe. While I was excited about floating the river, all that kept coming to mind were the “what if” questions: “What if I can’t get in the river?” “What if I have to go to the bathroom?” “What if I get stuck on a rock?” “What if I flip over?” “What if Dan and I get separated?” And, God forbid, “What if I drown?”
Just as that last one really sunk in, Peggy jumped into our van.
“Hi, are you ready,” she asked.
Well, no I thought. I can’t fully use my legs and left arm (damn MS) and you only need 4 inches of water to drown. So no, I thought, I’m not ready. Isn’t it funny? Sometimes you think MS has made your life so crummy, but you soon find yourself realizing you sure would hate to lose your so-called crummy life?
“Ready as I’ll ever be!” I told her confidently. I knew that these wonderful friends of mine put a great deal of effort into planning the perfect trip down the river, which was exactly what I wanted. So I put my faith in them (and God). I let it go. I trusted them all.
We left Buckley’s after getting our group together and drove to the perfect spot where I could transfer from my wheelchair onto the tube and then into the river. This spot was a private residence Sue had staked out.
We all were impressed, “Gee Sue how’d you get this perfect spot? I mean, what did you have to do to get permission to get on the river here?”
“Oh, I just asked.” she said with a smile.
Dan stood me up from my wheelchair. A nice employee from Buckley’s put the tube behind my back and together he and Dan, with some help from the group gathered there gently plopped me in the tube.
I was giddy! I couldn’t stop giggling and kicking my feet. “Oh my goodness, I’m really going to do this!”
One strong, deliberate push down a little embankment andSPLASH, I’m in the river. The water felt a little cold, brisk and so refreshing. Sue used a rope to tie my tube to her kayak; she was towing me down the river. The rest of our bunch got into their kayaks. I was the only one being towed and getting to float. Pretty nice, huh? And now, do you understand why I felt like royalty?
And I floated.
It was beautiful! Calm, cool water. Warm sun shining down on me. And strong healthy, vibrant green trees lining the shore. And it was so peaceful, gloriously quiet and peaceful. A feeling of just me and nature. Of course, I was with my friends and Dan but in those few quiet moments when I wasn’t shrieking, “I’m doing it! I’m really on the river,” it was me and Mother Nature. It was so comforting.
For those 45 minutes that I floated the Chippewa River, I was normal. My having Multiple Sclerosis played almost no part in my floating fun. For that glorious sunny Sunday afternoon, I was on a level playing field, so to speak. My disability wasn’t apparent. There wasn’t a wheelchair in the water letting people in on the fact that I no longer walk. I appeared to be just as able-bodied as anyone else; I had sort of forgotten what it’s like to kind of blend in. Well as blendable as a woman shouting “I’m floating, oh wow, I’m floating!!” can be.
That afternoon was the highlight of my summer and no matter how many “thank yous” I say, they’ll never be enough to thank Buckley’s and my church family – The Can-Do Bunch (Sue, Gary, Peggy, Charlie, Sue, Dave and Dan) – enough!
And it really was one of the last nice days of the summer 🙂
You are amazing, awesome and inspiring. You personify “Yes we can” and are proof that we can continue to particippate in so much that life has to offer. Thank you for being all that yu are.
Michael
Jennifer,
That is great! It sounds like you had a lot of fun out there on the river. I bet you can’t wait until next summer now.
Jennifer, I have so much to learn from you. You go out and enjoy life and see it through a lens that so many of us take for granted. You find beauty and excitement in things that I go too fast to appreciate. Thank you for sharing your experiences and I hope to someday appreciate what God has given me automatically – without thinking something could be better. You are a true gift to me and I haven’t seen you in years. Take care. Angel