Thank you for your thoughtful update. I'm sorry that your account was somehow de-activated, but I am grateful that you persevered to re-activate it and share your updated information. I am so glad that you were able to get a brain MRI and that it was clear

I strongly disagree with your UCLA oncologist's attitude that a full body bone scan "isn't necessary since the ASPS is pretty stable to slow growth, and you have no other symptoms to lead him to believe there are mets in your bones". Brittany's tibia met showed up during a period when her lung mets were relatively stable, and she had not experienced any symptomatic pain. You DO NOT want to wait until a met becomes symptomatic because once a met is causing symptoms like pain and/or numbness, it may be too big to successfully resect or treat with ablation or radiosurgery. It is critically important to monitor this unpredictable disease with complete and vigilant scanning of all parts of the body even if it may appear stable in other parts of the body. Unfortunately, too many oncologists are remiss in doing this, and too many ASPS patients suffer the heartbreaking and sometimes tragic consequences of the oncologists' lack of knowledge about the nature of this disease and their inexcusable negligent lack of vigilance in adequately monitoring it with regular scans.
Additionally, I am concerned/perplexed as to why your scheduled chest CT is being done without contrast since contrast is necessary to most accurately determine and measure any possible increased lung met growth. This is an important question for you to ask your oncologist.
My most special thoughts and very best wishes are with you for very good scan results which show stable disease and shrinkage of your lung mets, and I will be anxiously awaiting your update when your time and the situation allow. Take care dear Jen.
With deepest caring, healing wishes, and continued Hope,
Bonni