Hi there, are there any other NK T Cell non Hodgkins lymphoma people out there? I am the very rare patient to match my rare diagnosis: a 35 year old very white female.
When my diagnosis was finally reached (after many hospital stays and procedures and thanks to a brilliant doctor at City of Hope) I was told they had to call a university in Asia to get help on my treatment plan.
I'm 5 years in remission currently and dealing with the chaos that cancer left behind. I'm glad to be here but I don't know where I kind of stand...in....life