Very Sensitive
keepnthefaith
Member Posts: 36
I was wondering if anyone else had had a problem with Folfox causing severe bone marrow depression. Oncologist said he had only had one other patient as sensitive to the drugs as I am. I started Chemo on July 1st and to date I have only had 3 treatments due to very low White blood counts each time. I am on my 3rd round of Neupogen which cause lots of bone pain. Oncologist has decreased the chemo dosages twice and now I am beginning to worry that I am not going to be able to handle a therapeutic dose. The crazy part is that beyond feeling very tired, I am not having any other bad side-effects from the chemo (I know this is a blessing).
Background: I was dx with Stage IIIa rectal cancer in May 2008. Had resection then 25 radiation txs and the chemo. I am very frustrated with all this as I am a person that likes to be able to plan ahead - guess that may be the lesson that I bring away from all this - "life cannot be planned"....my husband would probably love me to learn that one. By the way, he is wonderful.
Thanks,
Felicia
Background: I was dx with Stage IIIa rectal cancer in May 2008. Had resection then 25 radiation txs and the chemo. I am very frustrated with all this as I am a person that likes to be able to plan ahead - guess that may be the lesson that I bring away from all this - "life cannot be planned"....my husband would probably love me to learn that one. By the way, he is wonderful.
Thanks,
Felicia
0
Comments
-
Bone problems
Felicia, i'm there with you. I have severe osteoporosis, and soft bones from my treatments. My other doctors say it's from all of the radiation.
I just found out today that this is a rare event. I don't know if my problems are the same as yours; no one has said anything about bone marrow, but i think it's just plain rare to have any bone involvement at all.
I'm frustrated too because i just finished my treatments, and i also had big plans for my life. Now everything has to be put on hold indefinitely. I have an insufficiency fracture in my tailbone, so Disneyland is out again this year.
I figure i can't realistically complain; i don't have metastasis, i can walk, so be it short distances, and i'm alive! But i truly do know how you feel.
They have put me on fossamax to prevent any further bone loss. I would ask your onc about that.
Many hugs,
Krista0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.7K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 308 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 395 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.3K Kidney Cancer
- 670 Leukemia
- 792 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 236 Multiple Myeloma
- 7.1K Ovarian Cancer
- 59 Pancreatic Cancer
- 486 Peritoneal Cancer
- 5.4K Prostate Cancer
- 1.2K Rare and Other Cancers
- 537 Sarcoma
- 727 Skin Cancer
- 652 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards