My Little Bs Have the Big C

A Breast Cancer Blog For Young Women

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“Bell” Of The Ball

Lymphedema sufferers, this is our time! We need to seize the day! Gone (for now) are the days of sleeves that are too tight; that constrict our already restricted flow. Dare I say, lymphedema fashion is en vogue?  Bell sleeves, slouchy sweaters and kimonos are in! And I just can’t get enough.  Like seriously, I have $2000 worth of clothes in my Anthropologie cart (narrowed down, embarrassingly) that I’m waiting to go on sale. But there’s so much to choose from! I might need to start a GoFundMe for a new wardrobe!!! I just can’t help thinking that I should stock up now before everything gets so skinny and tight again.

I have gathered an array of clothes that I’m just simply in love with that will let our arms breathe and that we will look absolutely adorable/beautiful/sexy in. All of the tops I have chosen all come from stores or websites where there are several styles to choose from, not just one. I tried to represent a range of budgets, from the very affordable to sell your kidney. Whatever you decide, if you end up getting one, send me a picture. I’d love to see it!

To say that I’m obsessed with everything on Anthropologie right now is a gross understatement.  They have so many options for beautiful tops that would be comfortable and forgiving on any lymphie arm. And right now they are having a 20% off sale on all tops and sweaters!

ASOS is an amazing site with too many choices. I find that some of their clothes are a little “out there” and trendy but they also have some wonderful basics and statement pieces. I love this site because they range from very affordable to pricey and carry a range of sizes including petite, tall and plus size lines. In their search bar I put in “bell sleeve” and “kimono” but just a basic search of their sweaters and tops revealed a plentitude of options.

I’m starting to really adore Eileen Fisher. The look is so easy going. I’m obsessed with the velvet wrap dress. All the clothes, though, are very expensive but I’ve heard the quality is great so if you can afford a piece or two, it will probably be a staple in your closet for years. They also have outlet stores so, maybe you can get lucky there.

I recently went into Madewell in Williamsburg, Brooklyn and was really impressed by the style and quality of the clothes. I was so excited to see so many choices in lymphedema friendly styles. I think they’re pretty affordable as well.

Oh Target, how do I love thee? Let me count the ways! I can’t ever leave target without a ton of stuff in my shopping cart. And these days, they have so many choices that fit so well. I just can’t help myself!

Finally, if you type in “bell sleeve top vintage” or “bell sleeve sweater” on etsy, you get an array of amazing and affordable (mostly) items that are one of a kind. Now, of course you don’t get to try anything on this way but oh, my god!!!! It’s so much fun!

So, I think I need one of those closets that Carrie got in the Sex and the City movie in order to get all the stuff I want.  It’s never going to happen but I will get some.  I’ll post when I do.

Where do you shop for clothes that fit your Lymphie arm?

If given the choice, what would you buy from above?

Do you have any great resources to share? Share in the comments below.


The Scare + A Goodbye

I should start this post by saying, I do not have cancer again. (Let me repeat that for my own reassurance.) I do not have cancer again!!! But a few days ago, I wasn’t so sure.

It began last Thursday, when after PT for my lymphedema, I had a pain in my armpit. When I went to feel it, I felt a lump. I asked my PT if she felt it too, and she said she had. I panicked for a second but then convinced myself that it was likely a cyst or ingrown hair. I’ve had them before and they usually go away in a day or two.

But 4 days later, it hadn’t gone away. It didn’t even change size. I mentioned it to my husband, who felt it too and said to call my surgeon right away. I said that I would in a few days if it didn’t go away. But as the day went on, I started to get a pit in my stomach. I started to panic. I began wondering if this was all starting to happen to me again.

I tried to stay calm by reminding myself that I just had a clear MRI a month and a half ago. Surely that would have picked up on a lump that size. I also tried to reassure myself that I would have noticed a lump there before since I’m always stretching out the cords in my axilla.

But what if the lump was hidden underneath one of the cords that just broke. What if the cords have been hiding it and, now that they’re gone, it’s allowing me to feel it.

This thought began to take over. I was doing the dishes and suddenly I was hysterical crying. My husband came to me and asked me what was wrong. “It’s back! I think it’s back!”

It was a Sunday but I immediately wrote to my breast surgeon and oncologist. I didn’t care who wrote me back as long as someone did.

My surgeon got back to me that night, said that it didn’t sound worrisome but to come in anyway to have it checked out. I felt good that I had someone looking out for me but I was terrified that this was all happening to me again. AGAIN!

I started to make plans in my head. What would I do if I had to go through this all again. NO! I could not do it all over again; the surgeries, the chemo, radiation, all of the appointments… I don’t have it in me. But what if I don’t have a choice? What if it’s more than a lump? What if it’s all over my body? What if this is it and I find out that I won’t, in fact, get to see my son grow up? What happens then?

It’s all I could think about. Having to tell Oliver that the cancer was back. That I was going to be sick. And that, one day, who knows when, I wouldn’t be around anymore.

I was paralyzed by my emotions and fear.

My appointment with my surgeon was for Tuesday right before 1:00. My aunt came with me for moral support but we were both climbing out of our skins. I couldn’t believe that this was happening to me again. I tried to have some perspective but, when you have been through a trauma and it happens again, there is no perspective. Just tunnel vision and all I could see was cancer, cancer, cancer.

I was called into the office an hour late (they had squeezed me in). My surgeon came in to feel the lump. She felt it but said it felt like it was in the skin.

“No! It’s deep,” I said!! “It goes down deep!”

“No,” she said. “That’s not deep. That’s not a lymph node. It feels more like a cyst. But we are going to do a biopsy and a sonogram just in case. We can do it right upstairs. For peace of mind. Is that ok?”

I had known and prepared myself for this. I figured she’d want a biopsy. But now that she was actually saying it, I started to shake. But I agreed. I needed peace of mind.

My surgeon is on the 4th floor of my hospital and the biopsy is done on the 10th. So I hopped the elevator and there was no one in the waiting room. “Carrie Ellman-Larsen?” They were ready for me whether I was ready or not. My aunt had to stay in the waiting room and I had to go in alone.

So much of what we have to do with cancer is alone. I always knew that but it felt more vulnerable this time.

I entered the room where I was going to have my biopsy. I nice, small woman came in and began to search for the lump. First, she thought it was my scar. I redirected her finger to where the lump was. “I feel that. Ok.”

She turned on the sonogram machine and began looking around. “It’s mobile,” she said. “It’s hard to pin down.”

“Is that good?”

She found a smaller tool for the sonogram. When she found it, she pointed to the screen. “There it is.”

“There what is? What is it?” I didn’t dare ask out loud.  But there was something to be seen.

She then went to get the needle. She said that the needle would be even thinner than the ones we use to take blood. She said that she would stick the needle in, leave it in for about ten seconds to get a sample and then repeat the process.

My shaking suddenly stopped. Self preservation?

The needle pinched when going in, then there was an achy feeling while collecting the sample. But, thank goodness, it did not hurt.

When she was done, she took each sample and put them in between two slides. Then she said, “I’ll be right back.” The lab was literally in the next room. I would know within two minutes if I had cancer again or not.

The shaking began again.

I texted everyone to keep busy but also to let them know that the biopsy was done and that I was just waiting. I really needed the time to fly by. And it did.

A doctor walked in. “Oh, shit,” I thought!

“Well, it’s completely benign. It’s what we call ‘fat necrosis.’ It can happen after breast cancer surgery. It’s very common.”

I let out a huge sigh of relief and began to cry. It was over and I was ok. I didn’t have cancer. The fear just swept out of my body as if taken by a huge wind and was replaced by huge relief.

I went back down to see my surgeon who was happy as well but had a feeling that it was nothing. I go back to see her in six weeks for a follow-up, just in case. But already, the lump has shrunk in size significantly, although I still feel for it several times a day.

This experience has reminded me that we are never done with cancer, even if we technically are. We are imprisoned by our fear of recurrence. We know it can come at any time. We see it happen to our friends just as much as we see lifelong remission. We’re standing on a ledge and we don’t know which way we will tip. For now, my feet are still on the ground.

Which brings me to the goodbye portion of this post. As many of you know, Beth Caldwell passed away this week. I only knew her through her blog posts. I commented on hers, she may have commented once or twice on mine. But that was the extent of the relationship.

But I knew her best as a fierce advocate for Stave IV breast cancer. Despite her own pain, she co-founded Met-Up and testified for more research for Stage IV. She was an educator, a leader, a wife and a mother. Her daughter is in Kindergarten, just like Oliver.

I know she didn’t want to leave her family. She loved them so much. And when we see another one of our sisters pass, we see ourselves in them. We know that one day it can be us.

So, what are we going to do about it? Advocate. Demand money go to research for Stage IV. Donate. Hug our children. Do the things we love in life. Smile more. Take risks.

These are the things we can do to honor those like Beth.

Beth, thank you for all you have done. You will not be forgotten.

Fuck Cancer!!!!!!