Rest & Recovery

After nearly three months in New York which included major surgery and a daily battle with nausea (radiation side effect) for six straight weeks, Emily was thrilled to board a plane and return home.  However, returning to Los Angeles did not mark the end of recovery.  Rather, as we have learned over the past month, it’s going to be a long road.

Doctors told Emily she would experience fatigue as her body recovered from radiation, but nothing could actually prepare her for the extreme exhaustion.  For the first few weeks home, simple activities like walking from the living room to the kitchen or even moving from one couch cushion to another resulted in five minutes of catching her breath.  Although frustration had a few appearances, Emily managed to remain optimistic and set her sights on recuperation.

Even though she still has a way to go, Emily is starting to regain her energy.  She has provided her body with ample rest – 13 hours of sleep at night is the norm, and while awake she often spends a majority of her time on the couch following through on DVD and TV show recommendations.  She is increasing her lung capacity and activity levels by walking Ginny daily.  Needless to say, Ginny is the most excited of all that they have made it up to four blocks now.  We are encouraged that these effects are radiation related, and not due to the removal of her lung.  She was walking two to three miles at a time in the period between surgery and radiation, so we are confident she’ll be able to get back to that point and beyond.

Celebrating Recovery

A nice night out to celebrate NED and continued recovery progress.

Many of you have asked about the current treatment plan.  At the moment, no traditional treatments are being administered.  Once Emily became NED via surgery and radiation, it was determined that maintenance chemotherapy would not be needed.  We have researched many supplements that have benefits for lung cancer patients (benefits to NK cells, immune system, etc.), so we’ve been playing around with which ones Emily can tolerate, and she is now up to about 20 pills a day.

Although the past month has not been incredibly easy, Emily can state without a doubt that it is all worth it.  This past Tuesday, she had her first CT scan since before her surgery.  The results came back clear.  She is cancer free and NED.   Upon hearing the news, I ran around the house whooping and screaming in celebration.  However, Emily simply remained lying on the couch with a big smile and finally said, “That’s great to hear.  I knew it.”  She may be still regaining her strength physically, but mentally there is no one stronger than Emily.

Next Up:  The next CT scan will be in three months.

Much love.  Live in the moment.

Miles & Emily

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11 thoughts on “Rest & Recovery

  1. Hello you two!!!! That is a beautiful posting, Miles. Hats off to General Ginny, too, for being the “pacesetter dog” that she is !! Continued rest & recuperation, Emily, and you, too, Miles. Our love & steady thoughts are following you through this strong journey together. Much love, Linda, Dave & Elle Hammond

  2. You look beautiful, Emily! Even though you have to go slow for now, you’re still pushing ahead. I know you’re celebrating every step!

  3. Emily and Miles, We continue to be proud of you both and think of you often.To pass along Tom’s words…Breathe This Life…and do it day by day, at your own pace, and you’ll see that each day brings something to be joyful about. Love you!

  4. Emily and Miles: you both continue to amaze me in your wonderful optimistic attitude.I am so happy to hear you have no evidence of disease.I raise my glass to you.

  5. Miles my alternate son (hahaha) and Emily! Happy happy joy joy. Jerry and I send you more good thoughts and wishes.

  6. Wonderful news! We are so happy to hear about your clear CT scan! Sending lots of good wishes for steady improvement, and a big hug for all of you. Love, E&J

  7. Congratulations on every step you take! Thanks for the update and photo of you both looking so
    stunning and ecstatic…I have been waiting this wonderful news. 🙂

  8. Hi my special special people……As someone who lives in the moment too I can’t agree more with you Miles……Each inch that Emily can go is an inch she couldn’t go yesterday…….Funny how everyone around Emily now knows just how much those little things mean. The real gift here is Emily and her family and friends. The perseverance and resolve that you have all shown to stand by her side has given her tremendous strength to do some unimaginable things. You are teaching people just how much can be accomplished with love, loyalty, kindness, strength and just pure WILLPOWER…….I am so happy and honored to be part of Emily’s team of supporters and there is nothing I wouldn’t do for her……… Sending you much love and admiration! C u next week!!! xoxoxo

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