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A Case of Mistaken Identity

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Look at me, I’m bald!

With 10 years of life as a bald woman behind me, I’ve experienced my share of head turns, inquiring comments, unwanted stares, and assumptions that my hair loss is chemotherapy related.  The attention used to stress me out big time.  Alopecia is sudden so requires instant adjustments.  As an Alopecian, I’m not physically sick, I just lack hair.

Early on as a bald woman, I was easily traumatized by the negative attention, but  as time passed, I became immune to the comments and questions regarding which type of cancer I was battling.  I came to realize that curiosity and its hopeful root, genuine concern, is just a part of human nature.  I’m no longer bothered by people wanting to reach out to me with kind words and prayers and am okay with being asked to go to the front of a long line or other acts of kindness based upon wrong assumptions about my health status.Ah, but how life’s chapters can chip at those hard-earned layers of emotional wisdom.

Recently, my mother was diagnosed with Lymphoma and is receiving chemotherapy.  I am both her advocate and caretaker during this difficult journey.   I take her to her oncology visits and her infusion sessions.  As much as I thought I was finally comfortable in my own hairless skin (and head scarf), walking into an oncology practice  as a bald person feels a bit like a time capsule trip back to day 30 as a bald woman.

http://static.howstuffworks.com/gif/destroy-cancer-cells-1.jpg

As I sit, stand, walk at my mom’s side, I am repeatedly asked “Which doctor are you here to see?” or “What time is your appointment?” or “Are you here for the doctor or the lab?”.  I’m having trouble ignoring the sympathetic looks from other patients as well.  I want to shout, “I don’t have cancer!” but how inappropriate would that be with a waiting room full of cancer patients?

It seems it only takes a new back-drop like this for my “bald sensitivity barometer” to sky-rocket once again.  I thought about wearing one of my “Understanding Alopecia” t-shirts, but Alopecia is so poorly understood and such a publicly unknown disease, my t-shirt would probably just prolong the stares as they wondered what is this terrible (possibly contagious?) condition I suffer from.

http://www.cancernet.co.uk/images/woman-chemo-very-small.jpg

For me it’s baldness, but you’ve undoubtedly experienced similar unwanted cases of mistaken identity or episodes of public attention for physical attributes you’d erase in a minute if you had the power.  How do you handle such situations?  Mom is only 1 chemo session into her treatment, so I have a whole lot more episodes ahead.  Any advice?

Susan Beausang, 4Women.com

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strawberrytech 5 pts

I have experienced moments like this though totally different at the same time, being diagnosed with multiple sclerosis about 10 years ago when I was 20 years old people thought I was drunk!

I remember having trouble standing/balancing yet not being able to get a seat because I 'looked' so young and healthy.

I imagine that having people think you are sick and then meeting you is inspirational to people, to be so vibrant and healthy would crush both their communicated and silent assumptions/judgements and to then interact with you would help open their minds to realizing we're all different.

Alopecia is something that I have heard of, both considered autoimmune conditions I have spoken on panels with people who have Alopecia. One of the things I learned on this panel is that one in five of us has an autoimmune condition...that is a big percentage of the population and if you count obesity as the epidemic I think it is the numbers go waaay up.

My point being that I think it's good you are able to stir peoples expectations and break the norm to open their eyes a bit. I appreciate you accepting and being proud of yourself.

:-)

Kristin
--
KristinBennett.com ( http://www.KristinBennett.com ) :: Where it all comes together...

Emsxiety 5 pts

I have Alopecia areata and lose it in spots around my head. I am lucky in that I can use my hair to cover up the spots.

I like the idea of using the Im with her shirt.

Jagged Edge of Em's Anxiety ( http://emsxiety.blogspot.com/ )

kyooty 5 pts

One of my son's friends has this too. She's beautiful with or without her wigs and hats.

ModaMama 5 pts

I'm actually not bald but I cover my hair for religious reasons, frequently with a headscarf. When I travel this is often mistaken for covering baldness and of course illness. I am embarrassed that I've drawn this attention and usually after only a short time I make the effort to find a hat or some other way to not be noticed with misdirected sympathy. Where I live, my scarf is entirely commonplace so it doesn't attract the unwanted stares.

At the same time, my mother-in-law has survived many onslaughts of cancer and I have close relatives and friends who've lost their hair in their own battles with cancer and its treatments so this misconception (even if it is only for a brief instant) makes me feel especially guilty.

So I don't know what it is like to be you, or not be able to pull off the scarf to say "see not sick" but I recognize this mistaken identity issue.

My suggestion, invest in an "I'm with her->" shirt and eventually the staff around the clinic will be able to tell that you're the support and not there for treatment.

www.SaraInAkko.blogspot.com ( http://www.SaraInAkko.blogspot.com )

Life in the Middle East, with craft and spice