Welcome note

When my husband and I set out to find and take pictures of wheelchair accessible waterfalls in every U.S. state, we were excited about the challenge. We gave ourselves no time limit to accomplish our feat; however, we had one mutually agreed upon rule that dictated how long we would stay in any given area. That rule was to never shiver again. Needless to say, adhering to this rule presented a new challenge. The new challenge was to find a waterfall that was actually flowing. Visiting mid-west and eastern states during months that prevented us from shivering are the same months that are hot enough to dry up streams; hence, little or no water flow for waterfalls. The natural scenery and picturesque landscapes warrant a second visit in the early spring right after the snow melts.

Bob and Jan

Bob and Jan
Christmas Eve

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Saturday, August 27, 2011

New focus for What Now Jan blog

For the past two years, I've written about the progression of Bob, who had a ruptured brain aneurysm and brain surgery. He has beat all odds and has survived with little damage. I believe the damage will correct itself over time. The damage is only his short term memory loss. Many times, Bob doesn't remember what we did during the day. He, also, still thinks he's in Iowa. The past five years that he has been in Oregon have been misfiled in his brain. As soon as the file is found, five years will be regained.
This blog will take a new focus. I recently had a procedure done called CCSVI, Chronis Cerebro Spinal Venous Insufficiency. In layman's' terms, my jugular veins weren't working properly. They weren't allowing an adequate amount of oxygen to flow to my lower body; hence, my muscles weren't working properly. The procedure is not a cure for multiple sclerosis, but it is supposed to alleviate many of the symptoms.
I had the procedure two weeks ago. My progress so far is an increase in humph. I'm not as content to sit in my wheelchair. I feel every ache in my butt and legs when I sit too long. I guess that's a good thing; however, since I've sat in a wheelchair for the majority of six years, my legs have atrophy. I have little endurance, so I can't stand long. It's a double-edge sword for now.
Each week, I will post a "week-end" update to journal my progression. Keep your fingers crossed.