Sunday, August 8, 2010
Pain Management
The nurse requested that she stay another night in the hospital because they needed to work out a pain management plan for her that would be appropriate for use at home. Saturday was spent trying a couple of different medications, none of which did anything but make her a complete zombie who could still feel a great deal of pain. She hopes to be released from the hospital on Sunday with a new plan in place to keep her comfortable. I will try to keep the blog updated with new information as it comes to me.
Wednesday, August 4, 2010
My Perspective
As an observer of Emily's ongoing cancer treatment, this has been a particularly difficult couple of weeks. If there were one word to sum up the experience of these past 10 days, it would be pain. Physical pain for Emily and emotional pain for those of us who love her. It is upsetting for me to watch my sister dealing with this adversity and to know there is nothing I can do to ease her burden. Most of you already know that Em has decided to go on medical leave from her job in order to focus solely on her health due to some recent complications. She has been experiencing significant pain in her back and shoulder, which we had initially attributed to fluid in her lungs but after a chest CT, we discovered that the tumor in her lung had grown. Her two primary doctors are divided on her prognosis with one offering dire predictions and the other saying it is her tumor dying and she may feel horrible for a while, but it is part of the healing process. She certainly has been feeling horrible, there is no doubt about that! But through all of this crisis, she remains committed to her recovery and plans to stay the course of treatment that she has chosen. She has managed her cancer up to this point and plans to continue with renewed vigor. If there is one thing she has shown us all during the past 3 years is that she has unbelievable determination and the strength of character to follow through with her choices.
Sunday, March 28, 2010
Start Spreading the News....


Tuesday and Wednesday were packed full of doctor’s appointments. After a couple of years of visiting many different doctors with various specialties, Emily has finally found a doc who “gets it.” When she arrived in Dr. Gonzalez’s office, he already knew all about her history and was well versed on all of her treatments, past and present. He also knew all about the Hippocrates Institute and understood that program in depth. He was happy with all of the choices she has made so far and he was pleased that she was looking to enhance her treatment options. After doing extensive blood testing, he had lots of recommendations for her, including additional changes to her diet, detox and enzyme therapy. He told her numerous times that he has never seen a cancer patient whose overall health is as good as hers and he thinks she will respond well to his program. It is going to take some significant time and effort to put the program into use in her daily life, but she is certainly up for the challenge. She is excited to get started and feels a renewed sense of hope and validation that she has made the right choice in her cancer treatment.
Thursday, February 25, 2010
Emily's Fund

I have been approached by numerous people, asking if there is anything they can do to help Emily as she goes through treatment. Some of our family members created Emily's Fund, which will help finance her unreimbursed medical expenses.
To donate, please visit www.earlsphotos.com and click on Emily's Fund.
Previously on Abreast of the Situation.....
Now the first thing I thought when I heard the news was “uh oh, lung cancer.” As it turns out, it isn’t technically lung cancer. It is breast cancer of the lung – weird, huh? Anyway, after her previous bad experiences with chemo, she had already made up her mind that if any cancer came back, she would not pursue chemo as a course of treatment. She has done extensive research on treatment options and she is working with her Naturopath to find a healthy alternative to the standard protocols. Currently she is doing occasional IV therapy and infrared heat therapy twice a day in an effort to shrink the mass. She will get monthly blood tests and chest x-rays to mark the progress of this therapy.
Through all of her research, she came across a doctor in
If you are interested in reading more about the Gonzalez plan, you can check out his website at www.dr-gonzalez.com/treatment.