A good old friend of mine has been diagnosed with MPNST about 4-5 months ago. He is now after local rxtherapy followed by large resection surgery. Recently, 6 lung metastases were visible on his imaging so he just started chest rxtherapy but is already having blood when coughing.
The prognosis is not good, and I wondered if anybody had had an experience with MPNST, and maybe some insight or contacts
He is suffering and feels miserable, because of the rxterapy, side-effects of the drugs, the cancer itself, and he wants to end it all.
I was thinking to recommend him fasting but wanted to crowdsource some wisdom and strategic information for this good friend of mine.
Does having DBS reduce or eliminate the number of falls compared with before the operation?
Young Italian-Spanish speaker needs support 
Root Canals and PD
My perfect cousin…………..(intestine related)
Still skiing black runs 😎
