Morning ladies This is my first post but have found the forum really useful in the build up to having treatment. So thank you! I had lumpectomy and node biopsy a month ago, found to be invasive ductal grade 3 negative to all hormones but no spread to lymph nodes. I had my first FEC of x6 FEC-T on 1st August and so far have survived!! Then it's radiotherapy (80mile round trip everyday for 4 weeks) The treatment itself went fine, was in the department for 3 hours, was offered lunch whilst there. The other patients seemed quite happy too. I took my 21year old daughter for company which was a good idea. I had decided beforehand not to try the cold cap as my hair is very short and I have just prepared myself for losing it now. I have bought some nice head wear in readiness and have an appointment to see the hairdresser at the chemo unit next time I go to look at wigs, get some advice etc. The afternoon I got home The nausea kicked in and I took the metachlorpromide regularly that day. Was awake by 2am pounding headache and nausea so not much sleep had. Yesterday started the steroids 2mg x3 times a day and have got to say helped the nausea. Started feeling flushed in the face late afternoon and it is still the same this morning. Don't feel unwell though. Was awake again at 3am last night but did eventually get back to sleep. Appetite not been too good for a few days(no bad thing as need it to come off, not gain) just drinking lots of fluids to flush toxins through. Pee is less pink today!! Need to eat when take steroid so things like rice cake, banana, yogurt was managed yesterday. I am lucky to have lots of friends and family support around me and for that I am grateful. good luck to all you ladies out there going through it as well. Be brave, strong and take what the hell they throw at us next!!! 🌻🌻🌻🌻🌻🌻
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