4 days post first Taxol session - 1 down, 11 to go

2 minute read time.

I can't deny that since Thursday, it's been awful. Now I know that the diagnosis and the 2 operations were a breeze compared to what is happening now. On Friday I felt high with energy, I believe it was the steroids, soon to wear off. On Saturday I started feeling slightly feverish, sore throat and aching arms, I was so tired. We were taking my husband  out for a lunch and I know if I mentioned I was unwell, he would not have gone. The girls were looking so much to celebrating Father's Day and his birthday, it was a good distraction for everyone. I made it through lunch, they didn't even suspect I was unwell. However, by Sunday evening, I was in A&E as I still had temperature. I didn't think anything of it as it was just flu-like symptoms but apparently it's dangerous as my immunity is very low. I was even quarantined once I arrived at A&E as they didn't want me to catch anything from the other patients. Even though I had my portacath put in, they still had to stick the dreaded cannula in my arm as there was no one trained to use the port in my chest at the local NHS A&E. So I was back on a drip with antibiotics and painkillers. But the bloods were not too bad and no sign of infection so I could go home at 2am with antibiotics for my sore throat/temperature.


Now we have to worry about whether or not we should be cancelling our week away late summer, by then I will be on week 9-10 of treatment but they said that the side affects of the type I am on (Taxol) is sometimes cumulative so there could be a lot worse to come. As well as the 'well known' symptoms (hair loss/thinning, nausea), I'm was warned about the loss of nails and 'bone crushing' pain and neuropathy (numbness). I feel like I would resemble a scene from the Fly where his nail peels off!


The girls would be so disappointed if we cancelled our little week away and technically I would not have to do anything except relax all day and eat! I know it's no exotic holiday and only Europe but it's our first full week away together as a family in 7 years and I am desperately for The holiday to be the highlight of this summer for the girls, not how bad mummy is looking. They've been talking non stop about it since I booked it early February (2.5 months before I got diagnosed). My husband is obviously concerned after last night. We shall see. I hope we won't have to. If we do cancel, I feel like I've given in to cancer but I'm determined not to let it take over my summer. The travel insurance company said I can cancel right up to the day before travel so I still have plenty of time to see. I could be ok, I won't know. Fingers crossed!


I know this is all to stop any further spread of the micromestatasis they found in the lymph nodes and they said they aim to cure and to prevent recurrence, I just hope they're right.

Anonymous
  • FormerMember
    FormerMember

    Hi 

    I was on Taxol… Paclitaxol ( think i have spelt it right ) It was the steroids that caused the biggest problem for me - No sleep and i mean NO SLEEP.  I had it weekly, a wednesday and took the steroids for 3 days after. By the sunday i was like a walking zombie. Oh and constipation but i took Movicol for that and if it got really bad  i would take sennakot too.

    The numbness in the feet and fingers tended to come and go, sometimes worse than others but nothing to complain about. 

    I was told to keep my nails painted as that can help stop any loss of nails, I didn't  loose any of mine and it was a good excuse to treat myself to some new nail polish … we are worth it !!!

    I did loose my hair but I had 3 wigs .. I thought oh well lets try a few new styles and decide each day is it a long hair day or a short one.

    I go to a local support group Breast Friends, and its nice to meet other ladies and chat and its not a depressing cant in fact we have quite a laff. I was recently asked to model ( No I'm not a model ) it was all ladies who are going through treatment who modelled for 2 local boutique and the function helped raise funds of the group. We had fun.

    As for your holiday I wouldn't make any decision yet. If you do decide to go make sure the insurance company will cover you. If they won't but you still want to go then I have recently taken out a policy with Boots ( got my points too ) and although there are a lot of medical questions they cover me while taking chemo. A policy for a week in Cyprus ( came back yesterday so i have holiday blues ) was £46. I am planning on booking another holiday now for around september - now i know I can do it … the world is our oyster so they say. 

    Maybe you could delay one cycle of chemo to be able to take that holiday.

    Hope you get on ok .. stay positive. 

    Janette

  • FormerMember
    FormerMember

    Many thanks Janette.