New Page

I’ve added a new page.  If you have specific questions you’d like to see addressed, they can be posted in the comments section of that page.  The page is open for discussions by all who wish to participate.


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If you break a bone, or have a heart attack, or are sitting at a stop sign and get struck by a car that was travelling 60mph, it’s really nice to have timely access to a doctor.  When you live a healthy lifestyle and are blessed with luck, you don’t need to think about doctors.

Before I was referred to a rheumatologist, I didn’t often think about doctors or access to health care.  This pretty much sums up how I viewed the topic:

I recently made a comment on AF’s board that generated more private messages than I’ve received in quite a while.  Thank you, all, for the support.  I really appreciate it.

Since then, I’ve been thinking (believe it or not, that happens occasionally).  What if people don’t want to see my A2HC references here, any more than I want to see the topic on AF’s board.

So… Is Access to Health Care an appropriate topic for this blog?  Why do I write?  What makes a good blog?  What’s the purpose of this blog?  Why am I blogging at 3 a.m., instead of sleeping?

Easy questions first:

Much as I would like to do some sewing for my daughters, I try to avoid noisy activities when the rest of the family is asleep.  There aren’t too many things I can do that wouldn’t awaken people, so I sit at my computer and type.  (Only someone without RA would ask why I, too, am not asleep.)

As readers of my blog, you’ll realize that I’m not necessarily qualified to write on the subject of what makes a good blog.  Fortunately, two bloggers that I follow are, and have pretty good posts on this topic.  Read here and here.

Which brings us to my real questions.  The main topic of this blog is living with this *$%@& disease.  I don’t really want to regurgitate medical facts that could be read elsewhere; there are links on my sidebar.  My purpose is more of a, “how does this affect day-to-day life?” and “making the best of things, given a bad situation.”

Access to health care, unfortunately, is one aspect of living with rheumatoid arthritis.  If you have RA, your life will be significantly better if you have healthcare.  “Ignore it and it will go away,” works for minor sniffles.  Home treatments work for nearly everything:  washing cuts and keeping them clean so they can heal without getting infected, rest/liquids for colds, and acetaminophen/ibuprofen for headaches.  Not so with RA.  Ignoring RA, or relying exclusively on home treatments, doesn’t work.  It leads to severe pain, deformity, the inability to walk, and a shortened lifespan.

When I started this post, I thought I would say that there would be no future posts about access to healthcare.  But A2HC is crucial in dealing with RA, so there might be occasional posts on the topic.  I’ll try to keep it focused, I’ll try to be balanced (not political), and I’ll try to remember to issue an ostrich alert.