New to the Group

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Morning

I’m new to this group, so not sure how things work! Also not sure how much info to put down!! 

so will just go with this for now and see where we go from hereThumbsupx

  • Hi Trudi, welcome to the group. If you click on my name you can see my biography and what my journey has been like so far. You can let us know what you have been diagnosed with and you can ask questions about it and others who have the same / similar diagnosis can help with their experiences. It’s a scary and worrying time for everyone but we can all support each other to help us get through the journey
    Hugs from cuffcake x x x x x

  • Hi Trudi, welcome to the group. Same for me, my journey is in my bio and you share as much of as little as you like. It’s helpful to hear stories from people in the same boat and post questions no matter how silly you think they are! Good luck with your journey! 

  • Sounds like you’re a little hesitant to jump into the forum; we’re all different and prefer to “vent” in different ways! Just know that we’re all here and will do as much as we can to make this journey a little easier. It’s sometimes difficult to open up to those closest at such a difficult time and that’s where this forum comes in. If you find yourself in a shi**y place log on and say what you feel like saying! All the best to you xxxxx

  • Thank you for your message! I read your biography you’ve been through the mill haven’t youCry I have just finished all treatment but feel out on a limb to be honest! 

    i will figure out how to write up my biography too rather than writing it each time! 

    thank you for reaching outHeart️have you had any further news on yours? 
    xx

  • Hi Mazz

    Thank you for message, it means a lot that people reach out to you! I have a loving supportive family around me but sometimes they just don’t understand plus I don’t want to talk to them about it most of the time! 

    My treatment is now finished but I’m still sore all the time etc etc!! I will go figure out how to write up my biography so people know a bit more about me!

    thanks again

    xx

  • I’m fine now (I hope), I had my last chemo in April and my last radiotherapy in June. I’m now on Anastrazole for the foreseeable and (fingers crossed) I’m doing OK on it, no major side effects. In a way I feel very positive about my experience, it’s certainly given me a more positive outlook in as much as I’m definitely living every day to the fullest whilst I am well and feel well. Because it’s brought it home to me that we’re all going to expire from something someday and I’m just thankful that it’s not my turn yet and I’ll deal with any cr*p that comes my way when it comes and not before. Chin up and try not to overthink things, don’t waste today worrying about things that may never happen. Hugs and good wishes to you xxx