Biking my way through radiation
I also started back at work part time at the Sierra Club. That has been good, but it’s hard that right as I’m catching up on things and making plans I have to be out again for surgery, scheduled for Nov 8.
One of the pelvic tumors was growing the first 2 weeks of radiation, but now it has stopped and my doc expects it to stay that way until surgery. I’ll also likely start a new chemo as close as 2 weeks after surgery. Not sure about what type yet but should know after my next appt Oct 26.
Fiona started kindergarten, and it’s going great. She is at a Spanish immersion school, which is part of Columbus public schools. She is making friends, counting to 100 in Spanish (with some help from her dad), and copying all the words she sees around the house. She says her favorite part is riding the bus home! She even won the Buen Gaucho citizenship award in Sept for being responsible. :) We got to attend the assembly and also showed off our LL Bean modeling skills. π
Nora is doing great at daycare. There are a few babies in her classroom now, and she loves helping to feed them and take care of them. She also likes to pretend to be a baby when she's at home. Holding onto her youth!
We've been enjoying the cooler weather the past few weeks. Tessa and Brooklyn visited, and we got to pick pumpkins and go to the zoo! We all had a fabulous time, and the cousins loved partying together.
Ali and Julie came to visit the weekend before, and we went apple picking, tried out coffee shops, ate the best South Indian food from Dosa Corner, and rode bikes to radiation.
In September, we participated in Steps for Sarcoma, one of the largest single fundraisers for sarcoma research in the country. Liam's parents, Janice and Mike, joined us along with our Cbus friends the Ferrell Schotters. I got to meet other survivors I know from an online group. And we had waffles, hot chocolate, and face painting! The girls insisted on princess dresses for the 1 mile walk, of course.
Our friends from Tacoma, Adela and Chris, visited right before my radiation started! We had some wonderful adventures, including Friday night wrestle fest.
We've also enjoyed time with Cbus friends :)
Those August scan results were difficult to take, but we've still been able to enjoy the past two months, especially due to all the love and support from our friends and family. I tend to focus on the positive in these posts, but I will admit how hard things feel sometimes. My own grief and anger and fear come in waves. The other day I was shopping with Fiona for her school clothes, and we were waiting in line behind an adult woman who was thanking her older mother for getting her pajamas. I thought about the possibility that I might not get to spend time with Fiona and Nora when they are adults, and I felt engulfed by a wave of sadness. I try to let myself feel these emotions and not hold back. Other times, the grief/anger/fear is just lapping at my ankles. Always there, but not enveloping. I heard this metaphor for grief on the radio, and it really resonated.
We are coming up on the 1 year anniversary of the diagnosis on Nov 5th, so I'll post again around then.
Sending so much gratitude and love to all of you.
xoxox
Molly
I’m so happy to see you absorbing and navigating the totality of this experience, and so appreciate the metaphor. Big hugs and love for ALL of it. Here cheering you on from California. Just keep π♀️. πππ
ReplyDeleteSo great you can bike again! Hugs.
ReplyDeleteThank you for sharing, Molly! Fi and Nora are taking after you and Liam in all of the unsurprising ways: model citizens, taking care of others, and so knowledgable about the world! :) Thank you for sharing about your grief and emotions; your approach to feeling them out is such an inspiration for living a full life of all the dimensions. Love you girlin
ReplyDeleteLove you always, Gina. Your words are inspiring and real, and I'm glad you're navigating those mixed and sad emotions. Seeing your precious kids and all the fun activities with your awesome friends in these pics is a pretty amazing reminder to live life. Keep spreading that love and light you do so bountifully. Xoxoxoxo, Libba.
ReplyDeleteAndrea and I are holding you in our hearts.
ReplyDeleteThanks so much for all the lovely pictures and the updates. Most of all, we appreciate your honesty about your feelings and your incredible strength. Much of that, I'm sure, comes from the lovely and supportive family you have with you. We still miss you in Pgh but you brighten our lives even all the way from Columbus. Stay in touch, keep us posted and know that you are in our thoughts daily. This is from both Emily and Mel.
ReplyDeleteAbove is only anonymous because Mel is a dope at this stuff.
DeleteSending all my love to you, Liam, and the girls. Praying daily for you.
ReplyDeleteThank you for these updates, Molly! How wonderful that you are biking. You have such a beautiful family. Robin and I are thinking of you and sending you love and light from Pittsburgh.
ReplyDeleteMolly, thank you for sharing your journey and the wonderful photos. XO
ReplyDeleteMolly, thank you for sharing these colorful daily moments as well as the difficult details of your treatment. 25 sessions, I had no idea that radiation could go on like that! Molly Nichols gladiator. Your girls must bring Liam and you a steam train of curiosities and laughter, great to see Tessa and Brooklyn as well. Love from the McCords and thinking of you always. La bicicletta in full effect!
ReplyDeleteYour spirit is magnificent and filled with light ❤️
ReplyDeleteThank you for sharing your journey, Molly. You are a model and inspiration in so many ways. You and your brairΓ² family are in our hearts here in Italy. Sending love and strength. - Cara U
ReplyDelete“Beautiful family” :)
DeleteI love these pics of biking on the trail! And your matching flannels for Fiona’s buen gaucho award, you all are adorable :) I like the metaphor of grief coming in waves, and it lapping at your ankles. I am here for you when the waves come to listen, or whatever helps the way through. You are such a great mom! We all had such a good time on your walk! It’s good to hear the radiation started to do it’s job, and we will be thinking of you during your surgery next week!!!
ReplyDeleteThis was me Molly F by the way!
DeleteMolly, We've followed your journey this past year and do wish you all the best for your surgery next week. Love the pics of you, Liam and your beautiful princesses.
ReplyDelete