October/November/December 2009...
Most of my life I was VERY presumptuous about being healthy, taking my (mostly) GOOD health for granted...
I was committed to annual check-ups for all of us, and so late October 2009, my daughter and I went for our annual and very routine physicals.
Surprise, surprise... my routine blood tests revealed extreme Anemia, significant White and Red Cell issues, low Platelets, and a variety of other CBC red flags! I was (stupidly) not worried when my GP doc left repeated phone messages to contact him, and when we did speak, I (stupidly) requested postponement of his referral appointment to the Hematology Dept until the end of the Fall academic term.
Arriving for my first appointment Dec 14, 2009, I was confronted with the check-in sign that read: "Hematology/Oncology"... What? Nooooo! not me... I must be in the WRONG place! And so my diagnosis journey began with vials and vials of blood drawn "stat", urgent Dr consultations, a surprise and painful Bone Marrow Biopsy, a full body Skeletal Scan, more blood tests stat, and then on 12.30.2009... THE revealing meeting... the "huh-what" moment ... the confirmation diagnosis that I, Julie, have CANCER!!!
Happy New Year to me, I just learned a new vocabulary word:
Multiple Myeloma!!! MM, Multiple Mye-what-loma!!!
January - June 2010
My medical metamorphosis began.
I read, and read, and read and researched and researched MM. I trusted my expert Oncology/Hematology team's plan and began my "New Normal" as a cancer patient.
My treatment plan was developed to include powerful Dexemthesone steroids paired with Revlimid chemotherapy, with the plan to be hospitalized for an Autologous Stem Cell Transplant July 2010.
I began living "one day at a time" like never before.
Jim was a wreck. Alissa and Scott were stunned; family and friends shocked.
Me... Cowgirl Up! I got back in the saddle and knew I was in for the ride of my life!
I did well on my initial pill-form Revlimid Chemo, "roid-rage" Dex Steroids and other supportive meds. I am forever deeply grateful and appreciative for all the love and support from everyone in my personal and professional life! I thank all of you for working along with me, and allowing me to continue to lead a semi "normal" life!
YOU have helped save my life!
My treatment trail ride forks to City of Hope hospital as I will saddle up beginning June 9, 2010 for a new rodeo called an Autologous Stem Cell Transplant!
Ye-Ha, let the adventure begin!
So glad you're getting a few fun days in! I'm not sure what to tell you to expect, physically speaking, at COH. I didn't get sick at all from the chemo until well into my 3 weeks there. The whole COH experience is pretty amazing. They really know what they're doing & do it in a most gratious way, treating the whole family as well as the patient. I look back on my stays there with happy memories for the most part. Keep your posts coming & I'll keep the prayers up too.
ReplyDeleteHugs, Sally
Awesome! Glade to here your feeling good
ReplyDeleteAndrew
COC
Haha ... as always, you got me good! I'm thinking - WOW, she's in HAVASU?!?! OMG! Then I scroll to the bottom and see j/k.
ReplyDeleteYou're too funny, Julie! :) I'm so glad that you are doing so well with what's going on! I told you, you are AMAZING!
Love you tons and tons!
Must say you are a hoot! lol hehe I'm glad that your feeling better and even more so glad you made this page and sent me the link!!!! have to say say you are like numero uno and by far my favorite counselor!Keepin you in prayer
ReplyDelete-Brittany Reimann COC
Julie, Julie, Julie,
ReplyDeleteI think about you everyday! Thank you so much for doing this Blog. You are amazing, your attitude and sense of humor is incredible. Keep up the great attitude.
Love you, Judy
Lets start planning NOW!!! Those pictures are just a reminder of how incredible that lake/river is. You do have such a great attitude! Looking and feeling so good. What a great role model to others and me. XOXO Jan
ReplyDeleteHi Julie,
ReplyDeleteIt's so good to read your post and experience your personality and wonderful humor shining through!
Keep feeling better,
Nairy
Wow, you are dominating the cytoxan! Sending domination your way! -Phil
ReplyDeleteJulie! im so glad i stumbled upon this blog. i knew u were going through some "health issues" per ur auto response on ur email. however, i had no idea. u are such a strong woman and such a wonderful fighter. i loved reading about u and now that ive found it, i will stay tuned. i hope we can meet up soon. love to you and yours. xoxo
ReplyDeleteThank you for doing this for all of us. I love you and send you lots of hugs and encouragement.
ReplyDeleteSo happy you had a chance to get away before your surgery and spend time with your family. Hang in there...we are thinking about you.
ReplyDeleteJamie