Hello, everyone......the last couple of weeks with no chemo has been a pleasant respite. We got to have some Halloween fun with The Cat in the Hat, a Princess and a Dinosaur....Melrose Halloween parade and Trick or Treating in West Roxbury. Alan made a special "cocktail" for the adult trick or treat companions called "The Nightmare". I did not have one...stuck to cider and candy.
We took three days last week and went to the Berkshires for our "getaway". It was a nice change of scene; the foliage was shades of gold as it faded into November. By Thursday when we left in the pouring rain, most of the leaves were gone. We stayed at our timeshare at Bentley Brook at Jiminy Peak ski area which is midpoint between Williamstown/North Adams and Lee/Stockbridge/Lenox. So we spent some time in Williamstown at one of our favorite museums, The Clark. The next day we spent in Stockbridge at the Norman Rockwell Museum, another favorite.
We arrived home in time to get gussied up for Sarah's 30th birthday party which was a fabulous event hosted by her husband Matt, who really knows how to throw a party. It was in the pentouse suite at the new Liberty Hotel ( formerly the Charles St. jail) which overlooks the Charles River. Can't believe our "baby" is 30. And even better that Carrie & Paul and Brooke and Alan were there, too.
So, we'll gloss over the rest of the week-end and the horrendous Pats/Browns game. My Patriots earrings, which have brought them good luck this year, will have to be replaced with a different pair for next week.
So, today, Monday, November 8 was the first day at Boston Medical Center and starting the new clinical trial. It seems like a long haul (and it is! Could be up to a year...), but I'm glad to get started. One day at a time! From my totally unscientific and non-medical background, it seems that the Melphalan and Revlimid (chemo drugs) are both attacking the bad plasma cells...one from the inside and one from the outside. Not sure what the steriod (Dexamethosone) is supposed to do, but I found during the last trial that it did help my energy level and appetite. Unfortunately, it also wreaks havoc with my fluid levels, especially around my lungs and heart, and legs, so the doctors need to keep a close on on the lab reports, weight gain, etc. I will also be more susceptible to blood clots and a lower immune system, so will need to skip the flying and will also need to be careful who is around me, especially this winter with flu, colds, etc. Air hugs for all!!!
I was so good at the doctors today that "Daddy Steve" got me a treat on the way home from the hospital....a vegetarian burrito from Chipotle!!!! mmmmm....I ate the whole thing! Don't know when I'll be able to eat one of those babies again! But I"ll have the memory........ :)
So, that's it from me tonight. As my friend Lisa told me, this is the "new step of my recovery" which I thought was a great way to look at it!
Thank you again for "following" this blog, keeping us in your prayers and thoughts, your cards, meals, visits and LOVE!
xxxxxxx
Cilla
Exactly...new step towards full recovery! But since when do you call Dad "Daddy Steve"??? :-)xoxo
ReplyDeleteWe will keep praying for good results from this trial. I am sure your up beat attitude will help.
ReplyDeleteLynn
Quite frankly Cilla, I miss Steve's description of your stools. So glad the new chapter has begun. We look forward to seeing you in a couple of weeks.
ReplyDeletexo
Kathy and Jeff
Kathy- We all know more about Cilla than we ever thought we would! And we still love her!!
ReplyDeleteGlad you and Steve had a nice mini getaway and that you were able to enjoy Sarah's big day. Happy Birthday Sarah!!
Lisa
Cilla-
ReplyDeleteMy thoughts and prayers are with you as you enter this new phase of treatment! Love you and I'll call soon to check in!
Carroll Anne
Good update. Keep on pluggin.
ReplyDeleteJackie and Steve
Keep up the Good Fight... We're all pulling and praying for you!
ReplyDeleteBob Starr
Cilla:
ReplyDeleteHugs from Atlanta! We can't wait to see you in a few weeks. We love you and think of you often.
Brooke & Jonathan
Cilla and Steve:
ReplyDeleteNew beginning are good. And this new beginning will be great for you. Keep the amazing spirit you have. This disease picked the wrong person.
Love ya,
Pat
Cilla and Steve,
ReplyDeleteGlad you had a nice week off to enjoy time together. Sounds like your baby's 30th was a great time and Halloween with your grandchildren was excellent therapy for you both!
Now you are back to the medicine and new trail with renewed spirit and strength!
Love to you both, Linda Tucker
We love you, Cilla!!
ReplyDeleteThe Fellows Maine-iacs
Hi Cilla...You are sooo headed in the right direction! Sounds like you are doing well and you have such a great attitude! Keep thinking positive thoughts...your body is listening. Slowly but surely those silly amyloid proteins will get the message. They are dealing with the wrong woman! I'm still praying for you!
ReplyDeleteCheryl Kurtz
Hi Cilla,
ReplyDeleteMy prayers and thoughts are always with you. You will get through this. You are strong and have a positive attitude. Miss you!
Love Maggie
Hey Cilla,
ReplyDeleteSending you a ball of energy to tackle another buritto soon. We miss you at Church.
Love, Monica
Cilla,
ReplyDeleteI have been following your blog and have tried to post comments. I think this time may work. If not I will have to get some help. You have been in my thoughts and prayers all along.
Love, Dorothy