Our most precious Valentine's treat came five days late with the thankfully VERY GOOD!! scan results


Brittany's wonderful, very caring and supportive, and extremely knowledgeable Clinical Trial oncologist Dr. Sawyer told us that approval for Cediranib as a prescription drug for ovarian? (I think) cancer is being pursued in Europe, so that means that the continued production and availability of Cediranib should now VERY relievingly and gratefully be assured

Some of Brittany's Cediranib side effects seem to be somewhat dissipating such as her severe mouth sensitivity, but she continues to have headaches, fatigue, and abdominal issues with nausea, vomiting, and chronic diarrhea. However, her severe vomiting episodes requiring emergency hospitalization have thankfully been almost completely alleviated by her preventative bi monthly IV rehydration which I would strongly recommend to anyone on a systemic treatment who is suffering chronic severe nausea and vomiting.
We are very interested and encouraged by all of the new advancements being made in cancer research and treatments including the several new promising immunotherapy PDL and PDL-1 type drugs, and will be closely following them, but we of course will continue with Brittany's Cediranib treatment as long as she continues to have a successful response to it, she is able to tolerate it, and it is available to her. We are deeply grateful beyond words that Cediranib has now provided Brittany with the precious gift of Life and continued Living for the past almost seven years which was being devastatingly threatened in 2009 by her unresectable/untreatable met at the head of her pancreas and her rapidly progressing widely disseminated disease. Brittany is very happily married and continues to try to Live Life to the fullest with great passion, undeterred determination, and her usual invincible positive attitude, most recently returning to actively skiing which she had been unable to do for most of the past 14 and a half years since her ASPS diagnosis due to the immense demands and challenges of her incredibly courageous battle and the physical limitations of her debilitating surgeries and treatment effects.
Truly none of us know what tomorrow will bring, especially with this unpredictable and insidious disease, but for now we move forward on this very long difficult ASPS journey continuing to aggressively research, actively network and communicate with other ASPS patients/family members, share information, and letting the bright light of Hope lead us through each day.
With a very happy heart filled with great relief and joy, special caring thoughts and healing wishes for all of the ASPS Community patients, and continued Hope,
Bonni
