Susan's Blog

Wednesday, May 7, 2008

Ice Cream for the Soul

One of the moms here is pretty sick, and undergoing heavy treatments. I always liked her, because she helped out at the school a lot, and she has two very nice daughters. I didn’t know what to think when I heard how serious her illness was. I just felt scared, and sad, thinking about how she must feel, about how she might be leaving her daughters soon. I have been watching her quietly, secretly, wanting to help somehow, make her feel okay. We aren’t really friends, though, so any overt offers might seem to be out of kilter, or all about the cancer. I don’t want it to be all about the cancer; I am interested in her and how she is getting along, all of which was triggered by the illness, but —

So today I saw her on the bench by the main staircase at pick-up, and I smiled at her and sat down. We talked about the Baby Bellies, which her daughter had tried out. The girls in that grade are having trouble with meanness, and I certainly have noticed this in that group. So her daughter did not really enjoy the class yesterday. I was not surprised to hear that.

I was feeling good talking to her and so I then asked straight out but warmly, “So, how are you doing with everything?” And she knew what I meant. Her face changed for a second, a flicker of something, and then she settled back into her usual warmth and smiles and said, “Okay, just want to get through this part, you know, have it be over.”

I knew. At least, I knew what I could know about this. Then she said, “I mean, what else can I do? Crawl away somewhere and not do anything about it?”

Then I understood. People were often implying that she was strong and somehow doing the right thing by having her treatments, when to her it looked like the only thing she could do. This is the way I feel about Nat. I am not brave, or a great mother, or special, or anything different from anybody else. I told her this, and it felt good that we both had pain to bear that was uniquely our own and yet which we could understand in the other. I do what I have to do. There is no choice. I take care of him. End of story. And I hate it when people ascribe greater strength or ability on my part. It just is. Mother, child.

And for this woman, her work to get well simply was. It was what she had to do. She said, “I was hoping today I could get my girls to just come and have some ice cream with me.”

It was such a hot and sunny day and that image just lifted me right up. I felt envious of her, that she lets herself just eat ice cream and that she has girls to do it with. “Ooh, that sounds good,” I said, and I’m sure I did not convey all that I felt.

But later on, after reading a few things on sites like https://www.dreamscoops.com/tips-and-tricks/troubleshooting-homemade-ice-cream/, I got in my kitchen, I got out the Ben and Jerry’s Peanut Butter Cup and thought about that mom, and hoped she had managed to treat herself. I ate the entire pint and did not feel badly about it this time, because of her.

3 comments

I’m glad you connected with her. My dad was diagnosed with the Big C when I was just in 3rd grade. So many people avoided the subject and I always felt so weird about it. I think my dad did too.

Our thing was watermelon. The last month or so before he died, I would fix each of us a plate with a red, juicy slice on it. We both loved it so much. We also took naps together. Your blog reminded me of those wonderful moments today. Thanks for that.

I feel the same way about the pats on the back. Really, there is no choice. You do the best you can for those you love. End of story…

— added by Judith U. on Thursday, May 8, 2008 at 1:18 pm

I have a good friend who has two sons — one with autism and one with cancer. (The joke is that she’s a “double dipper.”) Incidentally, she says that long-term, the autism is worse than the cancer — at least the doctors have a treatment plan for the leukemia.

Among us autism moms, we are in awe about how she manages. But as the previous poster said, you do what you have to do. I would really hate to have to find out if I’d be capable of handling one more catastrophe. — Cathy in CT

— added by Anonymous on Thursday, May 8, 2008 at 10:28 pm

Jude –
Terrific comment. I love the naps part. Made me weepy.

Cathy in CT –I’m happy to hear about all the support you guys give her! I hope/believe my new friend here will be getting the same kind.

— added by Susan Senator on Friday, May 9, 2008 at 7:42 am