Cyberknife treatment question

Discussions about the illness, treatments, doctors, etc.

Cyberknife treatment question

Postby Futhey4 » Fri Dec 22, 2017 7:30 pm

Hi, my name is Kim F, from Anthony, Ks,
I will begin Cyberknife treatments on 12/27 to 3
Cavernomas that have had a recent bleeds, one is in my PONS.Has anyone had these treatments and what should I expect regarding side effects besides the ones the Doctors have told me about like, nausea, fatigue?
Posts: 1
Joined: Mon Mar 20, 2017 6:50 pm

Re: Cyberknife treatment question

Postby Elizabeth » Sat Dec 23, 2017 6:04 pm


Wishing you all the best!
Diagnosed September '09 with one CM centered in the right insular cortex/basal ganglia. Saw many, many doctors and had surgery 12/10/10 with Dr. Spetzler. I am thrilled to have this bleeding thing out of my head even though I suffered a stroke during surgery. Have had/ continue to make an amazing recovery.
Posts: 1676
Joined: Mon Sep 27, 2010 6:49 pm
Location: Los Angeles

Re: Cyberknife treatment question

Postby Michelle2000 » Thu Dec 28, 2017 6:58 pm

Best wishes, Kim.

Please come back and share your experiences with us.

18 year old son with brainstem CM resected in March 2010, CM at C2-C3,
CCM2 mutation; DH & BIL with multiples in brain and spine; (MIL - deceased spine & brain)
Posts: 720
Joined: Thu Dec 02, 2010 7:40 pm

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