
Just this morning I submitted my third patient support ticket to the Dignicap folks inquring what I can expect as I’ve been diligently wearing their cold cap during treatments. Certain they’re sick of me, sick of all the questions, like a child incessantly asking, “Are we there yet?” But I need answers and their experience to settle me down. Seems I’ve lost at least 50% of my hair at this point, with most of the shedding occurring last weekend. Even though their literature warns this will happen, with only half of my treatments behind me, if the shedding continues at this clip, I can’t imagine I’ll have a head of hair left by my final chemo blast February 28. It’s uniform at least and has thinned out symmetrically, though I find myself stepping lightly so as not to loosen any more strands. Shhh, don’t wake the hair! Crazy how obsessed I’ve become. My doctor thinks since I still have hair at this point that it will remain, and despite his words, I’m not completely sure.
Shhh, don’t wake the hair!
I don’t think I appreciated what I had
These days, I pull my hands around my hair and realize the scant covering I now have, an oily few strands deep extending over my scalp which plays peek-a-boo when a little wind or head tilt reveal the sparsity. I know this is temporary and I know these drugs are doing what they’re supposed to do. They attack fast dividing cells, which are both the malignant ones and the ones affecting your hair, and digestion, too. It all makes such sense on an intellectual level, but I feel self-conscious even going to the grocery store at this point, though thankful that the weather is cold and I can wear a hat indoors. I bought a second bucket hat, camel corduroy, another option for ducking in and out of stores, hopefully unnoticed.
