Am I the only one on the planet?
Comments
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my husband's treatment.
hello. my husband also had an oligo 2. but there is more to the story than that... it's all on my profile. please have a look and my husband's treatments on our "about me" page and let me know if you have any questions. we are still in the thick of it here. we heard that only 4% of brain tumors are oligodendrogliomas. it's nice to know others are out there.
my name is sydney.0 -
Thanksarkansasbrains said:my husband's treatment.
hello. my husband also had an oligo 2. but there is more to the story than that... it's all on my profile. please have a look and my husband's treatments on our "about me" page and let me know if you have any questions. we are still in the thick of it here. we heard that only 4% of brain tumors are oligodendrogliomas. it's nice to know others are out there.
my name is sydney.
Thanks for sharing your experience with me, I am 38 years old and live in Rochester NY.
Since this is pretty rare, it is nice to know someone out there is livin' and dealin' with this. I am scheduled to have Stereo Tactic radiation on the 24th of this month. (focused beam) and I am starting Chemo this week. Temodar. Lets keep updated. Thanks very much for replying.0 -
You don't hear much about stereotactic radiation around here...kenneuf said:Thanks
Thanks for sharing your experience with me, I am 38 years old and live in Rochester NY.
Since this is pretty rare, it is nice to know someone out there is livin' and dealin' with this. I am scheduled to have Stereo Tactic radiation on the 24th of this month. (focused beam) and I am starting Chemo this week. Temodar. Lets keep updated. Thanks very much for replying.
At least I haven't, and my friend, Sydney, said that you were going for it soon. After reading your message - you will think it is a breeze - can't imagine having an awake craniotomy. I had a craniotomy in August for a Grade II Astrocytoma where half of the tumor was ressected- then stereotactic radiosurgery in December. I am doing fine, not any side effects from the radiation, other than my face being swollen and puffy for about a week afterwards. The radiation is nothing, the halo itself that they used to keep my head still is what was difficult for me. Will they put a halo on you for the radiation?
I've been told by my doctor that we may not see any results from the radiation for at least six months, I was fortunate that my tumor is slow growing at this point, but that also accounts for the slow response to radiation.
Wishing you the best, take care. You will be fine throughout all of this - if I can handle it, anyone can!0
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