For journal purposes only:
Dear Family and Friends,
I have been dreading writing this email, but it is time that it needs
to be written so here goes. On August 2nd I had a routine mammogram.
I received a message that they would like to do an ultrasound and look
a little more closely. I was scheduled for the follow-up on August
11th. After the ultrasound I was told that I needed an ultrasound
needle biopsy to figure out what was going on. They couldn't get me
in for the biopsy until the 20th here in Santa Rosa. Jon called his
good friends in Las Vegas and I was on a plane that evening (the 11th)
to have the test done the next morning. By 4:30 that afternoon we
knew the lump was malignant. I went and met with a surgeon at 6:00
and he pretty much lined out what would become my life for the next
little while. I stayed over night so I could have an MRI done and
then returned to Santa Rosa on the 13th. We welcomed some new
missionaries on the 16th and that evening I was on a plane again to
Las Vegas for surgery the next morning. The surgery went very well.
I returned to Santa Rosa the next day (18th) and prepared to return to
Las Vegas on Monday the 23rd with my husband to visit with the surgeon
and an oncologist and see what they had to say. Wednesday the 25th we
went to the Stanford Cancer Center to have a consult with a breast
oncologist there. So, I finally have some news to share about what
will be coming up.
My tumor was 1.5cm big (stage 1). The margins were clear. My lymph
nodes were clear. My tumor was estrogen receptive and HR2-HRT (I
don't know) negative. My oncologist at Stanford told me I was cancer
free as she was talking to me, but that we needed to decide what we
should do to give me the best chances at staying cancer free for the
longest amount of time possible. Because I am so young (yes, people
still think I am young)! and pre-menopausal, it is a little
different. The decision was made that I need to have 4-6 treatments
of chemotherapy, 3 weeks apart, followed by radiation therapy,
followed by 5 years of hormone therapy (tamoxifin), followed by
another 5 years of hormone therapy. By doing all of this I have a 5%
chance of having the cancer return. That is all the clinical stuff.
I feel in my heart and in my soul so grateful and so blessed right
now. Many miracles and tender mercies have happened since the 11th of
August. As Jon spoke with Elder Clayton and shared this news with him
he said, "Now you know why you were called to Santa Rosa and not to
Uruguay." I really think we were called to Santa Rosa because "our"
missionaries are serving here with us, but it has also made it
convenient to get great medical care! The doctors that have cared for
me are all outstanding, and I have felt so confident in their
abilities and knowledge. I have felt the Lord's hand all along the
way and I know I will continue to be strengthened and blessed to
endure and overcome this disease. I start my first treatment on the
2nd of September. I should expect to lose my hair before my second
treatment on the 23rd of September. The doctor felt like I should be
able to handle the treatments well, being young (there's that word
again) and healthy. :) We will stay in the mission field. I have
decided if you have to get cancer, you may as well do it while you are
serving a mission. I have the added blessing of the faith and prayers
of 170 full-time missionaries, and people all over the world that pray
for the missionaries. I am hopeful and cautiously confident that
chemotherapy will be tolerable. We will see.
My gratitude and thankfulness must be expressed for my dear sweet
husband and wonderful children. Every single one of them have been
amazingly attentive and helpful and thoughtful over the last two
weeks. Sadie flew back and forth with me when I was getting my
diagnosis so I wouldn't have to be alone. Kristen came to Santa Rosa
to help me for a couple of days and to be with Jon and Hailey while I
was having my surgery. She had to feed the new missionaries on Monday
night and help Jon with the departing missionaries dinner on Tuesday
night (the day of my surgery). Tod and Megan spent the entire day at
my side on Tuesday while I was having surgery and share the news of
what was going on with everyone that knew. Tod has helped with
doctors and results and gathering all of the information needed to
take with us to Stanford. Megan came to be with Hailey while we were
visiting with oncologists this week. Hailey has been smiling, doing
dishes, making dessert for Zone Leader Council today and anything else
that I have needed. But, more than all of those things, I have felt
their constant strength and love and support for me. They have all
been actively caring for their mother. It makes me feel like I
haven't failed them completely (another tender mercy). They are
amazing people and I love them with all of my heart. They give me so
much to live for. :)
Jon is a fighter! He gives US a pep talk every morning while we're
getting ready. Having him by my side makes me strong and faithful and
believing! I am so blessed! I am so thankful!
This has gone on forever long. I apologize. I wish I could call and
talk to each one of you in person, but it has been pretty hard for me
to share the news. Sometimes I am great and sometimes I fall apart.
I never know when the tears will come. I want you to know I am not
afraid, and I know all will be well. I love each one of you! You
wouldn't be receiving this email if you weren't someone special in my
life! Thank you for being someone special! I would appreciate your
prayers as well in our behalf. They give me so much added comfort and
peace.
All my love,
Susan