A New Project

My work space… if I had a clean table, fingerprint-less laptop, and some fancy filter on my phone. AKA- it’s a stock photo.

Happy Wed-Nes-Day! (Any other adults out there who still have to sound this word out before typing besides me?) 😬

I hope that everyone has been mindful about practicing acts of self care since my last post. Or have at least put it on your radar, now that we’re aware of how important self care really is. Remember, we are all worth it!

So, I recently got a wild hair up my ass and decided that I wanted to start my “October Project” early. Like last year, I was planning to interview people in the C community. But this time around, I wanted to interview the peeps who help to support the C community via programs, organizations, etc. and not necessarily just those diagnosed- though I’ve found that these two things often intersect. I had planned to post one interview per day like last year. But as I thought about it more, I realized that I didn’t want to wait until October. Instead, I will be posting interviews from different foundations, programs, non-profits, businesses, organizations, etc. over the next several months. Hell, if I get enough interest, this could become an on-going deal.

Throughout the interviews, you’ll have a chance to meet the people behind the scenes and see just how dedicated and whole hearted they and the programs they represent sincerely are. My hope is that by showcasing each organization, more people will be able to personally find support or will have the information and can help to spread the word of these amazing people and programs.

The individuals I have been working with and gathering information from are truly special. If you find that you feel the same way and want more information or want to see how you can help, contact information will be provided. And if you know of any person or group that you would like to see included in this project and have a contact for me, let me know! I would love to be able to highlight them! Keep an eye out, I plan to post the first interview next week.

And a little note: You may have noticed that the domain name for this blog has changed from jessicafilloon.com to mamasgotthis.blog … This is in anticipation of another project I’ve been hard at work on. Stay tuned!

Grateful As F

Since I was a little kid, I have said the same prayer to myself before going to bed each night. “As I lay me down to sleep, I pray the Lord my soul to keep. If I die before I wake, I pray the Lord my soul to take” followed by all of the things I am grateful for. Even as a small child, I realized the last line was a little ‘much’ but it is what it is.

I learned the prayer from a small card that my mom had, which I eventually took over and would thumbtack above my bed. With my intense anxiety as a kid, this card always made me feel protected when I felt the most vulnerable.

If you read my last post, you know I have been working on simplifying my life and trying to be more present. I am proud of the little steps I’ve made. I’ve even crafted a morning ritual to help me start my day in a peaceful and grateful manner with morning meditation, me time, and self care. It has helped me tremendously with my attitude and patience! But it wasn’t until last night, as I said my prayer, listing the things I am grateful for, and thinking about this post- that I really listened to myself. It’s taken all these years to realize that I create a Gratitude List every night. I am proud of my evening ritual and bookending my day this way really works for me.

To continue with thankful and grateful traditions, I’ve created my annual ABC’s of Gratitude. Quick reminder, these are things I am truly grateful for, no matter how big or small and they seem. Here goes it 💜

A- Audiobooks

B- Braless-ness

C- Crystals and CBD Oil

D- Dance Parties

E- Essential Oils

F- Family and Friends

G- Giggles

H- Our Home

I- Instacart

J- Jobs I Enjoy Showing Up To

K- Kind People

L- Lists

M- Meditation and Meditation Apps

N- Neck Massages

O- Old Memories

P- My Planner

Q- Quiet Time

R- Dinner Reservations

S- Stretchy Pants and Swear Words

T- Team Work

U- Unsubscribe Buttons

V- Vegas

W- Warm Beverages

X- Extra Numbing at the Dentist Office

Y- Yoga

Z- Zero Drama Llamas

Happy Thanksgiving 🍁

My Friend Jamie

I met Jamie via the Kick Ass Cancer Mamas Facebook group.  Here is her story…
Tell us your story / stats:
At 5:30 p.m. on Valentine’s Day in 2007, as a 27-year-old, I should have been getting ready for a romantic dinner with my husband—where we would celebrate my 14-week pregnancy. Instead, I was in a doctor’s office, learning that I had invasive ductal carcinoma. I hadn’t been too worried a few days earlier, when I first felt the lump while taking a bath. I told my husband that this was a glaring omission on the part of the editors of “What to Expect When You’re Expecting.” Instead of dinner, I was listening to an oncologist explain that I had to start chemotherapy right away. Trying not to panic, I immediately asked how I could possibly get chemo while I was pregnant. I’d given up coffee, and now my doctor wanted to pump me full of poisonous chemicals? It seemed crazy. But after seeking out second and third opinions and doing my own fact-finding, we agreed to go forward. At 27 years old and 14 weeks pregnant, I was diagnosed with triple negative breast cancer, a particularly aggressive form, so waiting until I gave birth was not a viable option. Even though I had carefully researched my decision, once the therapy began I was paralyzed by fear that my baby was being harmed by the harsh medication. To bring peace of mind, my healthcare team came up with an innovative solution: weekly ultrasounds of my baby. During a time when I was losing my hair, my toenails, and my fingernails, it was a way for me to see he was okay in there. As long as he was still alive, I told myself everything would work out. I was six months into my ten month chemo regimen when our son, Blake, was born perfectly healthy. I imagine every cancer survivor is changed by the experience—but most of them don’t get the gift of a child at the end.
C aside, tell us about yourself. What makes you, YOU!
I am a mom, a coffee-junkie, a wife, a wanderlust, a friend, a neighbor, a lawyer, Hamilton-obsessed, a professor, a baseball fan, a runner, policy-optimist, and full of hope.
Thoughts on the pink… 
I am so grateful and proud of the work of these small but mighty non-profits, helping people living with and beyond cancer: National Coalition for Cancer Survivorship at http://www.canceradvocacy.org , The Pink Fund at http://www.pinkfund.org , Triage Cancer at http://www.triagecancer.org , Get In Touch at http://www.getintouchfoundation.org .
If you could send a message to yourself from 10 years ago… how would that go?
This is non-responsive to this question but . . . When I was first diagnosed, I would pray to God and ask him for kindergarten. I wanted to be there for Blake’s first day of kindergarten. Today, Blake is 11 years old and in the 5th grade. God is good, science rocks, and I am one lucky lady. The hardest part of joining the sisterhood, especially the sisterhood of young women with cancer, has been the tremendous loss and grief. My life is richer beyond measure for knowing these women and being blessed to call them my sister-friends, but my heart and soul aches for the loss.
What are you passionate about? Is this different than what you were passionate about before dx?
Access to healthcare. Families facing a cancer diagnosis, or any other chronic medical condition, shouldn’t have to wonder whether they can pay their rent or health insurance deductible this month. I am grateful for the work that organizations like the National Coalition for Cancer Survivorship (NCCS), Triage Cancer, and the Pink Fund are doing to reduce the financial toxicity facing too many patients today.
Do you have a favorite quote, mantra, phrase, or curse word?
I absolutely had a C mantra I said to Blake while I was pregnant in treatment. It is not original … I stole it from my favorite movie, Why I Wore Lipstick To My Mastectomy: We are the sky and nothing can touch us … We are the sky and we will remain unchanged.
If people take away anything from your story, it would be…
Hope lives . . . my hope is an 11 year old boy who has stolen my heart. 
*** Jamie kept a personal blog during treatment which may be helpful to other young mothers finding themselves on this journey-  www.pregnantwithcancer.blogspot.com.