Guest guest Posted April 13, 2004 Report Share Posted April 13, 2004 Hi - I posted my response to the " Neupogen Side Effects " post before I read your question. Your husband's response to Neupogen sounds like the same thing that happened to me - I detailed it in my message. I had no mets, just plain old muscle spasms, which caused mid-lower back pain that was beyond excrutiating. The worst pain I have every experienced by far. Far worse than surgery. But if your husband is experiencing the same thing that I did, it's not from the cancer it's muscle pain. Here are some things that helped me (drugs didn't help much): 1. Hot baths 2. Acupuncture (helped a lot) 3. Stretching 4. Ativan (this was my doctors idea - it made me relax a little bit which did help the pain some) 5. lidocaine patches - don't help that much, but take the edge off a bit. 6. Putting bags of frozen peas on my back (the freezer burn caused me so much discomfort that it made me forget about the muscle pain. 7. Oxycodone (helped a little but not much) Also, check with your doctor to see if your husband can get the number of shots decreased (for instance 3 instead of 5). Do know that if the pain is muscle-related it will go away once the shots are stopped (within a month). Please give your husband my best. I can certainly empathize with his situation. Regards, Jodi > I need some info and figure this is the best place to get some.Hubby > has been having GMCSF(generic for neupogen, etc...)shots to raise his > white blood count so he can continue the chemo with avastin.Had his > 5th(and last in series)shot this am.Anyway,about the same time he > started the shots he developed severe pains in his lower back.He says > it comes and goes like a spasm but is excruciating even with pain > meds that have been working very well until this.Because of his > spinal cord deficits he normally cannot feel muscle or surface pain > so I'm thinking this has to be tumor or organ related.We've not been > aware of any bone mets but his hematology has been so irratic the > past few weeks,I've been wondering....He thinks it's caused by the > shots because that's when it started but I can't find anything in the > side effects about causing pain and it doesn't make sense to me. I > know some of you on the board have personal experience with this drug > to increase the WBC and I would really appreciate any info you can > share.Also,info on bone mets would be appreciated,just in case. > His next appointment with the onc is 4/22 so I'm trying to gather > info prior. > Thanks!!!! > > (caregiver to Hubby,dx inoperable stage IV cc 7/03,currently on third > chemo regime) Quote Link to comment Share on other sites More sharing options...
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