Photo Friday – Pain Week 2017

Pain Week is an annual conference focused on pain for the health care professionals who see patients who have a multitude of disorders and diseases. Doctors, pharmacologists, nurse practitioners, and those who offer complementary and alternative therapies all gather to attend seminars on the latest research in this field.
I was there to represent US Pain Foundation and the INvisible Project. Spending time in the exhibition hall, I had interesting conversations with attendees about what they do in the pain community and how the various projects of US Pain could be a good resource to offer their patients.
During the 5-day conference, topics included ketamine, pain management coaching, regulatory issues, prescribing guidelines, biofeedback, virtual reality for pain management, microbiome, patient-centered practices and addiction. Disease specific seminars included erythromelalgia, arachnoiditis, occipital neuralgia, neuropathy, osteoarthritis and fibromyalgia. For the first time, the American Headache Society hosted an all-day seminar on chronic migraine education. More on that amazing program to come.
On this Photo Friday, I wanted to share pictures of what attendees wrote when asked the question, “What Did You Learn?” The creativity, thoughtfulness and important lessons represented below showed me that those in attendance were walking away with new ideas, skill or knowledge that would then be implemented into their practice when they returned home.
Photo Friday- Fluorescent Lighting=Hell
I found this is a cute little store in Philly. Truer words never spoken. When I was still working in an office, they had to disable the automatic lighting and I brought in lamps. Although everyone with migraine disease has the legal right to ask for workplace accommodations for their condition, not every company is…
Photo Fridays- Georgetown University Hospital
I have a special connection in so many ways to Georgetown University and its Hospital.
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Hot Off the Presses! Welcome to Golden Graine! The name of my blog is a play on my last name and slang for migraine (so don’t forget the “e” at the end of ‘Graine). When I had to stop working at the age of 32 due to intractable chronic migraine disease, I found purpose in…
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Katie,
Sounds like an excellent week! I really like the first response. This person listened and listened well! Living with comorbidities, especially those that are pain related, make living with migraine and treating the other pain conditions a real challenge.
Motion is lotion! Good one!
Hugs,
Roni