Susan Tanner’s tragic death from cancer April 24 and the loving response
on social media and in several publications demonstrates what an effect her
death has precisely because Susan had a greater, loving, professional,
intelligent, funny and more positive effect on us with her life.
Susan was known professionally for working for several major record
labels in New York, Boston and elsewhere, before returning to Buffalo to work
for Righteous Babe Records and Ani DiFranco for many years. I can attest to
Susan’s professionalism, knowledge and respectful treatment of others from my
time writing for several publications, and her industry background and regard
has already been written about well by Donny Kutzbach in The Public and Dale Anderson and Jeff
Miers in the Buffalo News.
Susan was also well known, and in the long run maybe better or with more
reverence, as the hostess with her husband, Marty Boratin, of what is basically
Buffalo’s rock and roll bed and breakfast, their home in Eden. The couple
hosted many house concerts, parties and other events, and gave accommodations
to many touring bands who needed and often could not afford a place to crash.
Regardless their day job responsibilities, Marty and Susan also fed and
entertained the musicians, seeking nothing more than some good music and
friendship in return. There are too many shows to remember, but among the
memorable ones I recall are Peter Case, Jon Langford, Oh Susanna, Gurf Morlix
and a host of local performers. Susan, an accomplished singer in her own right,
even joined Jon Langford (The Mekons, Waco Brothers) reciting poetry during one
of house concerts. Susan and Marty’s Independence Day and Christmas parties are
also legendary, bringing people back to Buffalo who moved away years ago.
There may be no one absolute way to fight and live with cancer, but
Susan certainly found one that worked for her and those around her. With an
intelligent, scientifically trained and educated mind and awareness, she
researched and participated in interviews and discussions about and in actual
treatment trials for her cancer. She frequently traveled out of town for these
treatments and consultations, and was very open about her cancer diagnosis,
status, treatment, how she was feeling and what stage she was in at that
moment. Having cancer was not going to stop Susan from using her mind, body and
spirit to fight this bastard and to live a full life, She openly and repeatedly
acknowledged she received primary health care and her cancer diagnosis from the
medical staff of Planned Parenthood, a group of dedicated professionals who
helped keep Susan alive. Friends and loved ones of hers have made financial
donations in her name to Planned Parenthood, a fantastic idea. During a
memorial celebration for Susan at Babeville, college friend, record industry
and radio colleague Anita West movingly spoke of their friendship, fun together
and their shared fights with cancer, probably sharing more than anyone else
could from that period. West came into that event blazing, wanting people to
know that much more about Susan and her life as well as know about the ups,
downs, loves and fears of living as they did and fighting cancer.
Susan Tanner recites poetry with Jon Langford, 2014. Photo by Barkloud Productions/Val Dunne Photography |
I can write of a bit of familiarity with Susan’s caring and sharing of
hopes and fears of chromic and terminal diseases. My lovely wife, photographer
Val Dunne, was diagnosed with multiple sclerosis 24 years ago, and fights it
every day; indeed, she is currently in an about 3-week episode/flare up of the
disease, and just returned to work. We have been fortunate to be friends with
Marty and Susan for longer than we can remember, more than 30 years (hell, my
sister Heather had Marty’s late father as a high school teacher). Val has been
through many trials, experimental drugs and treatments, even chemotherapy, and
like anyone suffering from chronic or terminal illnesses, a toll is often
taken. For the last several years, every time we see Susan and Marty,
particularly at their home, after a while Susan, Val and several other people
living with chronic and/or terminal health issues will start talking about what
they are going through, sharing information and empathy, offering advice,
solace, support and love. After a moment or so, I will leave these
conversations, because while I may be the spouse and partner of someone in this
situation, I cannot fully know what it is like to live with such diseases, and
I felt like a bit of an intruder; I was never made to feel this by any of the
other people, but I realize that there are experiences I cannot fully understand
without being the person in the crosshairs. Val and other people I’ve spoken
with who were part of these discussions always credit Susan with being
incredibly open, positive and supporting, sharing information about everything
from how to try to avoid nausea and bad tastes in the mouth connected to
chemotherapy and other drugs, which pains reacted to which medications and
other treatments, which medical staffs were more understanding and caring, and
what the best places to stay and best modes of transportation were for people
with health conditions. Oh, and of course, diet was key, along with gardening,
as were appreciation of good music in all its forms, good friends, books and
conversation. According to Val and others I have talked to with these medical
conditions, Susan was never short on warmth, understanding, shoulders to cry on
and a song to cheer them up. I noticed that talking with Susan raised Val’s
spirits, and indeed mine, during periods when her MS was really causing her
trouble. When Val was hospitalized with pneumonia a couple of years ago,
besides family and staff, Susan was her only visitor.
Susan and Marty were/are great people on their own, but made/make an
incredible couple together. Their home was warm, open and inviting, there was
always good food and good music there, beverages of all kinds and an
understanding that love truly conquered all.
Well done. I'm starting to cry right now.
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