Today Doug, his dad, and I summited the 14,259-foot-tall Longs Peak in Rocky Mountain National Park via the classic Keyhole Route. This was an important ascent for me. I had climbed Longs Peak once before in 2007 and had loved the route. When I was hospitalized for 16 days with my final severe UC flare last fall, I would often walk down to a common area that had huge picture windows facing west and gaze at Longs Peak in the distance. I thought back to the day I stood on its summit, and wondered if I would ever be strong enough to be up there again. Today, I answered that question as I successfully hiked 15 miles with about 5000 feet of elevation gain to reach the summit. This peak was different than the others I have done this summer, as it is graded a class 3 climb. This means that the route has some sections that involve scrambling, or using one’s hands to ascend the rock, yet the terrain wasn’t technical enough to require the use of a rope. There are also areas of exposure where a person wouldn’t want to fall. It felt wonderful to move over rock, and the experience made me look forward to the days when I can climb technical routes again. I just want to heal up a bit more first.
Everything with my ostomy went well during the hike and there is not much to report. I once again used closed-end pouches to eliminate the need to take time to dig a cathole and empty my pouch. This helped ensure that we were on the summit before the afternoon lightning storms came. This ended up being an important detail on this trip, as we dealt with one of the largest lightning storms I have ever witnessed in the mountains later in the afternoon. Fortunately, we had just descended to tree-line when the storm reached its peak intensity and avoided being caught out in the open.
The day before our trip, I discovered that our summit attempt would fall on the United Ostomy Association of America’s (UOAA) second annual Ostomy Awareness Day. I was thrilled! UOAA’s call for this special day is to have “Ostomates Unite and Help Others See Ostomies in a Positive Light!” This is a message that is very dear to me and is one of the reasons I created Ostomy Outdoors.
However, I have to admit that I have not always been as open about having ulcerative colitis or an ostomy as I wish I would have been. Truth is, when I was first in the hospital with my severe ulcerative colitis flare last fall, I hardly wanted to tell anyone about it. Sure, I shared the details with my family and closest friends, but I was less open with others. My coworkers were all curious about why I had suddenly disappeared into the hospital. I sent out vague emails to them telling them I had an auto-immune stomach condition. I was too afraid they might look up ulcerative colitis and see what the symptoms were. Once my hospital stay became lengthier, I did fess up and share the name of the condition. Surprisingly, it felt really good to not have to keep everything to myself, and I found that the people in my life were very supportive.
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