I was thinking the other day about how much rheumatoid arthritis is part of who I am. During and after my diagnosis I worked to accept that I had this and even embrace it.
But it's often a secret part of who I am. I can't go around having everyone feeling sorry for me. I don't want pity. When other parents see me lugging twins around it might look to them like a lot of work but they don't know about the pain that comes with it. When I look tired they don't know about the fatigue that I'd have anyway. Even when I do tell people, I tend to minimize what it means to my daily life.
I can't think of anything else that is such a big part of my life that is mostly hidden from others. I feel like some epiphany should come from this realization and I was going to post about it, if only I could come up with a point to make. Then yesterday I checked my arthritismom email and found out that National Invisible Chronic Illness Awareness Week is coming up soon. Oh heck, that's right, I'm not alone!
This year National Invisible Chronic Illness Awareness week is September 8-14. They have a website and a blog where you can read more about it. It's not just for the couple million of us with rheumatoid arthritis, but those with depression, diabetes, eating disorders and other chronic illnesses as well. They have some good articles about invisible illnesses and the issues you face when people don't know you are battling something every day of your life.
Mostly I think it's fun to say. National Invisible Chronic Illness Awareness week. It's a mouthful, but catchy.
Today it's not so invisible. My right foot is swollen and painful, my 11 year old stepson just informed me I am walking with a limp, just in case I didn't realize. I did realize. Hopefully I can get back to being the invisible arthritismom tomorrow.
Posted by
Jennie
on
August 23, 2008 at 11:03 AM
Categories:
Invisible Illness
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3 comments:
I loved your post. I think I will love them all. Twins! Oh my…
For some reason my feet are DOUBLE the size right now too--flaring badly in general... but my feet are deformed anywayplus I have ugly hammer toes… awful! I mean, I didn't even put on shoes yesterday and my ankles had "fat roles" (and no, I generally don't have fat ankles at least!) My son (5) said “I wish my toes curled way up like yours! I said, “no you don’t…” He said, "Yeah, it's funny."
oh, joy...
Lisa
I'm working on a post about Arthritis Feet. I need to get a good picture of my mom's feet if she's willing.
Hi Jennie, I recently found your blog. Been enjoying reading your posts and added you to my blog roll. I'm a newbie blogger, so it has been really great connecting with people.
I'm 36 and have had RA for 11 years. It is a funny thing that we work so hard to accept and embrace our diagnosis, learn to make different choices or live with more limited choices, but at the end of the day, it is often a very secret part of who we are -- even when we confide in (non-arthritic) folks about what we are going through.
It's a strange "idea" to balance and make sense of, especially when it is such a huge part of our lives.
Thanks for a thought-provoking post.
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