Hi friends! Wondering if anyone has supplemented their cancer care with IV VItamin C therapy. I work with an ND oncologist along with my regular one and she suggested it. If you have used or are using it, how often and at what dosage? Did you have any side effects? I'll let you know if I start. Meanwhile I had second round of Faslodex shots today so I'm going for a walk to move the gunk around!
Patty
Patty, there are alot of naturopathic docs who believe that high dose Vit. C is worthwhile with cancer. My onc doesn't agree with any these treatments. But I do. Good luck if you decide. Would be very interested in your results. My onc says Vit. D is important. 1000mg everyday. That's about it!
Hi Patty, Did you decide to go with the IV vitamin C? Just considering it myself... Thanks, Gill
Not yet Gill, I'm waiting for my labs next week. The Xeloda dropped my CA 15-3 a lot the first month and I want to see if that continues before adding another therapy. I'm still debating about IV C. It's quite a commitment of time and money. I do think it can improve energy and quality of life but I'm feeling great right now and would rather not spend another day at a doctor's office!
Re: CA 15-3:
My new ONC only draws one of the two markers as he says they’re the same-?meaning they go up or down together?? Any insight? Also he moved my CT scans to every 4 mos vs 3; which I freaked out about but then thought we’ll only 3 xs/year with my terrible “scan-dirty” that’ll be blessing in disguise...now I just gotta ditch the appt to see him every 2 mos; once with scan/bloodwork the other visit without (which is appt I’d like to ditch); I’d still do bloodwork! Thx for any input!😍
I hear you! Thanks for response. I'm lucky too in that I feel well at the moment and my disease is stable - just contemplating another line of attack!
That's helpful clarification, I wondered why some get the CA 27-29. I didn't have a prior history so have the CA 15-3 and the CEA, which doesn't seem as helpful or accurate as the CA 15-3. Regarding scans, I'd been getting them every 6 months but will probably move to 4 since the liver mets took off last spring.
About scans...I often see friends here referring to PET scans. I've only ever had CT's, and my oncologist said they don't use PET often. I wonder PET scans are more common with early stage or other cancers?
Port fitted & had 1st taxol IV
MRI and Bone Scan update (Stage IV BC)
Recent Metastasic Stage IV Breast Cancer
Anyone who has always eaten right and still got Stage IV?
Big C - taboo subject
