I don’t know what’s wrong with you people. Y’all seem to relish seeing my ugly hairs. You know how I can tell? Hairs Thursday tends to get the week’s highest number of hits from the website followers, and the number of Facebook responses are always robust. Get your fill of my horrendous hairs over the next few weeks, folks. They are doomed.
I can’t take it anymore. Even the ties and bow ties are tense about being around my coiffure. I can attest that it is horrifying to even sleep under my hairs. In fact, I noticed Suzanne is sick enough of the mop that she’s put her pruning shears on her nightstand. I think she’s trying to muster the courage to hack my hairs as I sleep. I’m smart enough to know that if she actually does the deed she will act completely innocent and claim she must have been sleep-haircutting. Suzanne’s a wily one, I tell you.
Anyhoo… Mustache Bow Tie o’ the Day got me thinking it’s about time to kinda have a neckwear theme, so I’m going to be wearing my mustache neckwear and accessories for the next week or so.
In one photo here, Bow Tie and I are simply showing you the clinic waiting room. Yeah, it’s not that exciting. I’m guessing there must be some kind of HGTV donation deal with the clinic though, cuz all of the televisions are always on HGTV. Plus, the waiting area has a zillion HGTV magazines. But I say, “Hey, if donations from HGTV help keep a mental health facility going, donate your little channel out.”
The other picture shows me and Bow Tie taking the purse for a walk and some sightseeing outside the Utah State Capitol building. We stopped there on our drive home from treatment this morning. My Diet Coke went along too, but it was too shy to be photographed.
FYI This morning, I completed my 18th TMS session. I have 18 more ahead of me. It feels good to have half of the entire series behind me. 36 seemed like a zillion treatments at first.
After this many treatments, I’m a little discouraged that I am not feeling significant improvement in my mood-leveling. I am still stuck in a tar pit of depression, unable to swim out. Suzanne and I think we are seeing some small changes, but so far they are so tiny that we might just be seeing through our wishful thinking-colored glasses. I talked with my TMS doctor yesterday about my discouragement. He thinks I’m probably about where I should be, mid-TMS, but we decided to lengthen each treatment from 20 minutes of electromagnetic head-pecking to 25 minutes, for the duration of the remaining treatments.
I still have hope.
