Yes. I was just diagnosed with this about 3 weeks ago. Actually on my post op from getting my right upper lobe of my lung removed due to lung cancer. I go for my post op only to learn I now have lymphoma. So I'm getting info and planning treatment as I write this. What is your story?
Hi, I was diagnosed in March 2014, just 6 weeks after my husband was diagnosed with Motor Neurone Disease. A double whammy to say the least.
Mine is in the lining of the abdomen so they couldn't operate. I've been having chemo RCVP since then. It started every 3 weeks, then I now have it every 8 weeks. It's now by a slow injection in my stomach, which they're trialling.
I got very tired about 3 days after with my first ones but now it just seems to last all the time. I think I've been very lucky but I am v v down at the moment. Doc says it's the reaction finally hitting me, because all the attention has been towards my husband and his condition and mine seems to have been sidelined. I've had to carry on and deal with all his stuff as well as my own. I think I've got 3 more sessions and the Doc seems quite happy but I just wonder when it will come back.
