Hi girls
While I think of it. Nausea - I was given a script and got it filled for ZOFRAN from my GP in preparation for nausea for my daughters wedding. I did take one the morning of the wedding cause I was feeling a bit queezy (nerves I think) but I haven't had to take them since but I understand they are a bit of a magic pill. They are not cheap........I paid $35.40 for 10 wafers but I didn't care. I just wanted to be able to get through my daughters "High Tea" and Wedding feeling well and I did thank goodness. They were magical days and nights and every time I think of the high tea and wedding now it gives me warm and fuzzies :-) which we need lots of them don't we?
When I think back now I did find the FEC a lot kinder than Taxotere. BUT on saying that I am getting much further into the whole chemo thing and my body is taking a bit belting on the chemo as we all will be going/have gone through. I have had a lot of side effects but I must say FOR ME!!!!! and please remember we are all so very different. That for me a few days with FEC I was comatose (and I not joking when I say that) and then I did improve slowly. With the Taxotere it is a different feeling and a different set of side effects. Some side effects are definitely the same but I do find (and again this is personally) that the nerve pain and bone pain is quite debilitating for a long time of my cycle. I did not find Panadol or Panadol Osteo even touched the sides of my pain (taking it from the start and regularly every four hours as suggested). That is why I have had to bring in the big guns in preparation for this onslaught (should it arise).
I also give myself a Neulasta injection for my low white cell count the next day after chemo and I know that also adds to my pain. I have never bothered to formally have myself diagnosed with arthritis but I am quite sure I do suffer from it and I feel that the pain seems to grab those areas where I feel I have arthritis. My sisters suffer with osteo and rheumatoid arthritis so I know quite a bit about it's problems and symptoms. The pain for me is not in one area of my body it seems to go right through every bone and nerve throughout the day and night making it hard to use a heat pack etc.
All I can suggest is to use the information through this wonderful site from all your pink sisters and also from your medical team and "be prepared" !!!!!!!!!
I really hope that has helped you girls as I know it is the "unknown" that is soooooo scary.
You can often access beanies, hats, scarves etc. through the cancer council, McGrath Foundation (if you have one over there) and wig centres. We have a Wig Service through Cancer Council here in W.A. where you can borrow wigs and all the above things for as long as needed and you just return them washed and in good condition FOR FREE and it is a wonderful wonderful service. We outlay so much through this journey that if we can save a little somewhere it is worth it. I don't like turbans, scarves and beanies on my funny face/head so I tend to wear hats and wigs when I go out. Nothing around the house YET but getting colder now unfortunately and I throw a hat on to answer the door if I need to.
Sending you some warm and fuzzies and healing hugs your way girls. I am lucky that I am having a "good day" so far. Must be the Dex hee hee
Mich xo