The last week of Arthritis Awareness Month had me writing about advocacy in two different spectrums (spectra??).
First, the Patients' Access to Treatments Act.This is an important bipartisan initiative to limit insurance companies from charging more in co-pays for Biologics than for other drugs:
"When you have rheumatoid arthritis, medication can be an essential part
of controlling the disease and managing symptoms. This is the moment
where those who are insured breathe a deep, relieved breath. At least
they won't have to worry about medication cost. Or will they?"
The rest of that post is here.
Also this week, I had the privilege of profiling ten amazing people in the inflammatory arthritis community, talking about what they do to advocate and raise awareness:
"Many people who live with rheumatoid arthritis are engaged in advocacy
and raising awareness in one way or another. Many more want to get
involved, but have limited energy or don’t know what to do. As part of
our celebration of Arthritis Awareness Month, we wanted to profile a
number of people who have found various ways, big and small, to spread
the word. We hope that these stories might inspire you by showing that
there is a range of activities you can do to advocate and raise
awareness, depending on your health, energy and time. All of the people
profiled do this is a labor of love by donating their time to the cause."
You can read the rest of that post here.
And now: weekend. I hope yours is wonderful.
1 comment:
I am very thankful for the coverage that my job provides, however by taking a biologic I have to abide by the schedule of the nearest IV infusion center. Orencia was great with the nurse able to come to my home but its exreamly hard to work with the Infusion centers restricted hours. I know I should be happy to be able to work, but sometimes I think the health care system would be much happier if I didn't work and could be at there beck and call for appointments... Sigh.... sorry for the rant :(
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