Brain cancer

[RichardSpencer]

Has anyone had brain cancer ?

[maddie86]

i havent but ive read a lot about it... i know its pretty bad, but i also know that people have recoverd from it... do u have it yourself?

[Smiley]

Re: Gbm grade 4 brain tumour My husband ,aged 47 was diagnosed with a GBM grade 4 in April 2010. He awoke with a stiff/sore leg, which progressively became weaker - 36 hours later we received the diagnosis of a brain tumor . He has had surgery, rehabilitation, radiation, chemotherapy & also stereotactic radiation. The initial tumor was on his right side , the second tumor presented below the original site 3 months after April surgery. We were advised that surgery was too risky on the second so continued with chemotherapy & 5 months later had the stereotactic procedure. My husbands left side movement is effected (has been since April surgery) and seems to be gradually deteriorating - he obviously cannot drive but continues to work as this is an important positive in this world of which he now feels he has little control. We have an amazing team of specialists caring for us and our oncologist and GP support us enormously - in that we are so fortunate. That being said though I hate it - I hate that this tumor has taken over control of our lives & changed the man I married. I feel so selfish sharing this because I know my husband hates it too - my greatest fear is what will happen & how. On the outside I am trying to remain positive & I haven't given up hope - but my husband and I are both realistic and understand that this is what will claim him - when is a anyones guess . I am not scared of being on my own but I am terrified of how this may effect our two amazing teenage sons. I seem to have garbled on but it does feel better & reading your posts have inspired me to contribute so for that I thank you

[Tash77]

My son is 18 and has primary central nervous system lymphoma and has one large tumour in his left hemisphere. He is a transplant recipient of a kidney at age 2 so the PCNSL is a direct result of long term immunosuppression. he is about to have his 1st scan after 3 doses of chemo to see is its working. we have been told that if its not working we don't have any more options for treatment and will be looking at end of life palliative care....very nervous to get the scan done and results.

[Tash77]

My son is 18 and has primary central nervous system lymphoma and has one large tumour in his left hemisphere. He is a transplant recipient of a kidney at age 2 so the PCNSL is a direct result of long term immunosuppression. he is about to have his 1st scan after 3 doses of chemo to see is its working. we have been told that if its not working we don't have any more options for treatment and will be looking at end of life palliative care....very nervous to get the scan done and results.