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Amy Stockwell Mercer

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Amy Stockwell Mercer

Tag Archives: empathy

Body Image from a man’s point of view…

22 Thursday Dec 2011

Posted by alsmercer in diabetes

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Chronic Illness, diabetes self management, empathy, inspiration, living well with illness, self acceptance, type 1 diabetes

This is a great essay about body image by Eric Lagergren of Diabetes Self-Management:

Show Me Your Sites :: Diabetes Self-Management.

He writes,

This is all a roundabout way of saying that I’ve gotten over most of my insecurities about body issues as time passes. I attribute this to age, of course. When I made my triumphant and committed return to the gym about a year and a half ago, I pushed through the anxiousness of undressing and showering in a locker room for the first time since my undergraduate days. That’s a long time away from being used to standing naked in front of a bunch of men. Perhaps it’s something you don’t give a second thought to, but being back in the world of the locker room initially made me hesitant, self-conscious. I was 14 again and just waiting for someone to say something that would ruin my life.

I know, right? Do we ever really grow up?

I have to admit that I love reading about a guy having body image issues. His honest description of feeling self-conscious about his body at the doctor’s office spoke to me. It reminded me that we all struggle to love and accept ourselves, pump and injection site scars and all, and that it is the sharing of stories that can give us a more accurate depiction of beauty.

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Picture Perfect Night…

12 Monday Sep 2011

Posted by alsmercer in Uncategorized

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Chronic Illness, diabetes, empathy, insulin, type 1 diabetes, women's health

I took the boys to my mom’s house yesterday afternoon so they could swim in the pool and I could sit at the edge of the water and chat with my mom. I invited friends to join us because it was a beautiful September afternoon, but still warm here in the lowcountry, and I knew they would enjoy getting out of the heat and into the water. And when we got there, it was one of those days when I don’t ever want to live anywhere else. A breeze blew across the river, keeping the bugs away, and my boys jumped and swam and splashed with sheer happiness. Even Reid, thick in the midst of the terrible twos, was having a good time.

When my husband finished work he joined us by the pool and had the brilliant idea of going out to dinner (I hadn’t been to the grocery store all weekend) on our way home. Even better, my mom and step-dad offered to take the kids to the marina restaurant in the boat. Dale and I got there ahead of the boaters, and sat at a picnic table with a view of the intracoastal and a glass of wine as the sun lit up the sky. It really was picture perfect.

By the time everyone arrived, they were windblown and hungry. We quickly placed our orders and leaned back in our chairs to admire the view, and as I reached for my ‘shot bag’ to test my blood sugar before dinner, I realized I didn’t have any insulin. It was one of those stomach punches of living with diabetes. Shit. There was no one to blame but myself. I hadn’t brought insulin to the pool because I figured we’d go home for dinner. And here we were with this perfect view on this perfect night, and I couldn’t eat. I asked for a to-go box and ordered another glass of wine. Thankfully I wasn’t very hungry, and the food didn’t look mouthwatering, otherwise it would have been worse.

It felt ridiculous though to sit there at the table with friends and family as the sun dipped out of sight on one side, and the full moon rose on the other, and not be able to eat. I was determined not to let it bother me, but today, as I sit here at the computer, I’m frustrated and weary. I’m inspired by people who say what doesn’t kill us makes us stronger, and I want to have that kind of attitude, but sometimes I am just so tired of having to think like  a Type A all the time. But I don’t have a choice. So I’ll do my best to roll with the punches, have a glass of wine, enjoy the view and wait to get home to eat.

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it could be worse…

13 Wednesday Feb 2008

Posted by alsmercer in diabetes, posted by Amy S. Mercer

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diabetes, empathy, worries

I remember my Grandmother telling me when I was sick that it could be worse, that there was always someone worse off than me, and so instead of feeling sorry for myself, I tried to imagine the children from Africa I’d seen on TV with their bloated stomachs and the flies buzzing around their faces and I knew she was right. Diabetes wasn’t as bad as that, right? But I didn’t know what it was like to be starving and living in a country where as a child, my life was vulnerable, and compromised, so really, how could I relate to their pain? I understood that Grammie was saying to toughen up, that things could be worse.

And sometimes in the summer at the lake in Maine, when Grammie wore a bathing-suit, I would steal a glance at her chest and the raised slash mark from her open heart surgery, and I knew that she was tough.

My parents are of the same mind, when things get bad, when someone is sick, we just soldier on, we will get through this, this is not as bad as it could be. Dad used to tell me when I had a cold, to visualize polar bears as my white blood cells (my parents were hippies) coursing through my veins, fighting the sickness. It never worked. After I was diagnosed with type 1, I remember Mom telling me to stop crying, crying wasn’t going to change anything. She cringes when I remind her of this and I wish I could just let it go. Maybe Mom and Dad are that way because they have 2 daughters with a chronic illness, or maybe they are that way because they grew up with parents who lived through the Depression and had seen bad times, who believed that it was a waste of time to feel sorry for yourself, who believed in being tough and so I never cried again about having diabetes.

But now that I am a mother, when I see my children in trouble, I am caught between wanting to wrap them in my arms and never let go, to make their trouble disappear through the power of my love and yet I also struggle not to tell them to stop crying and toughen up, that things could be worse. When my son is hysterical crying and hyperventilating because he is too scared to go to school at 6 years old, things couldn’t get any worse. I’m not thinking about the children with cancer or the poor children who are suffering in their individual, horrible ways, I am thinking about my son and that he is overwhelmed by his anxiety. And I would like for someone to acknowledge how hard this is. I would like for no one to tell me things could be worse, because right now, they couldn’t.

I think my parents put up a tough front about diabetes because they didn’t want my sister or I to be held back from a normal life, they wanted us to follow our dreams and not be defined by this disease and as a mother, I understand that desire.

But I wonder if things would be different if someone had taken me in their arms when I was diagnosed and said, yes, this is really terrible, this is awful and just let me cry as long as I needed. I wonder if someone had acknowledged how hard this disease is, if it might have lightened my load? So as I work through my son’s anxiety, I will do my best to hold him close and acknowledge his pain, I will tell him that I know he is hurting, I see his pain, and that it must be really awful. I will tell him that we will be there to help him.

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