Oncologist appointment tomorrow - what questions should I ask?

After being diagnosed on 18th January and going through all the various test, I finally get to see the oncologist tomorrow. Would like to hear from anyone who has any suggestions about what questions would be good to ask. 

Also what are your experiences of how long it took for treatment to start after first oncology appointment. As my breast cancer is grade 3 and fast growing, I'm worried about it spreading, before my treatment even gets started. 

Was it suggested you have a PICC line or port?

  • Thank you so much for you reassuring words Jolamine. I will give the breast care nurse a ring, they may well be able to give me some reassurance over the phone. As you say it's just a blip, I definitely need to get back to my walking. I'm also wondering if the new tablets could be affecting me a bit. I'm not sleeping so well, due to the hot flushes returning, since starting letrazole. I feel better already, now that I've decided to make the phone call, so thank you for that. Xx

  • Hi Pippin,

    I hope that the nurse may be able to put your mind to rest. I'm glad to hear that deciding to phone has already made you feel a little better. 

    I'm sorry to hear about the poor sleeping and flushes. This sounds like the side-effects of Letrozole. It took about 4 weeks before I began to feel the effects.

    Regards,

    Jolamine xx

  • I've been on the letrazole for about 4 weeks now. Did you find that the side effects improved over time? When I was first diagnosed I had to come off HRT, so GP gave me venlafaxine to help with the flushes. I could up the dose if necessary, but wonder if things might settle down over time. Xx

  • Hi Pippin,

    Many people find that the side-effects do settle with time, but sadly, this didn't happen in my case. I take Venlafaxine too and started taking this the year before I started Letrozole. At the time, I was taking Tamoxifen and I found that this really affected my emotions, whereas Letrozole caused me a lot of pain in my joints. Most of the hormone therapies have similar side-effects.

    I hope that you are one of the lucky ones and that you'll find the side-effects begin to settle given time.

    Regards,

    Jolamine xx

  • Hi Ladies,

    Sorry for radio silence again!..I am still here and still reading all your messages.

      Good luck with you radio today...not that you'll need it. Honestly i think it will be a walk in the park for you. Do take rest if and when you need...for me though radio was the easiest part by a mile and actually didn't have any side effects...so i really hope this is the case with you. Keeping eveything crossed for you. I can't remember how many sessions you're having?

    So happy to hear that you're not hosting Christmas this year, that will be a lovely break for you and i hope you get to put your feet up and be spoilt a little! Glad to hear you scar is healing too - hopefully you can get out for your walks soon.

    Sorry you're feeling a little anxious at the moment though,i think that's totally normal and i can HARD relate! I'm finding this part so tricky to deal with, all the homones etc affecting sleep too but also my moods, feeling pretty low and teary at the moment which is not me at all. It's scary...but i'm hoping my body will adjust to the drugs in time (my oncologist said 6-9 months!!!!!) but as long as i know they will, that is helping. I am feeling a little better this week...just so teary and i'm starting to bore myself!!..let alone my friends!!!!! But i'll get there i'm sure...think it's processing everything that's happened in the past year, looking at what the future looks like, worry of recurrence and then also dealing with my hormones being plumemted into menopause....oh and my husbands redundancy!...i've also got two poorly kids who were sent home from school!!....just cold/temp etc so hoping they'll be back in soon but it's just a lot...espeically this time of year...still need to finish off the xmas shopping!.....BUT one day at a time!!!

       How are you doing at the moment? I know your tilt test isn't too far away...how are you feeling otherwise? Have you manged to get all your shopping done?

      How are you? Hows the chemo going? Hope you're hanging on in there!

      ANy newsx your end?

    So sorry for sporadic responses i am still here!!!!

    Good luck today Pippin - you got this!!

    Take care ladies! xx

  • Hi Greeny80, I am having 15 sessions of radiotherapy and can now tick off number one. It all went smoothly, just the 3 hour round trip a bit of a pain. 

    Sorry to hear that you are also struggling a bit at the moment, with sleep and feeling emotional. As you say the change in hormones can have a big effect. Also you are right about trying to process everything over the past few months. I seemed so positive while going through chemo and surgery. Now I'm told cancer has gone, I seem anxious and worried, seems so strange. 

    I'm sorry you have the added stress of your husband's redundancy and 2 poorly children. I hope they both feel better soon. 

    I hope you start to feel better soon, just know you're not on your own. Always here for a chat, if you're feeling down. Xx

  • Hi Jolamine, it's such a shame that your side effects didn't settle over time, will have to see how it goes for me. If you don't mind me asking, what dose of venlafaxine do you take? When I came off HRT they said I could take 37.5mg for 2 weeks then up it to 75mg after that. At the time I chose to stay on the 37.5mg, as I new I would be going on hormone blockers, so would then have the option to up the dose at that time. I've certainly had an increase in hot flushes since starting the letrazole, which affects my sleep. Can't decide whether to increase the dosage or not. I have left a message for the breast care nurse to phone me today, feel a chat would be good for me. Realised I had a couple of things on my mind. I'm sure I'll feel better after discussing with someone. Xx

  • Hi Pippin,

    I take 150MG of Venlafaxine, but I understand that dosage can be up to 375MG in severe cases. I am glad to hear that you have left a message with the nurse and hope that she got back to you today. How did your first radiotherapy session go?

    Jolamine xx

  • HI Greeny,

    I am so sorry that you are having bother with your emotions and night sweats, on top of everything else. Unfortunately, this is not uncommon, but you will soon be back to your normal positive self. What a pity that you have two poorly children at home - hopefully, they'll soon be hale and hearty again. Hubby had a biopsy of his cheek on Monday, so we have an anxious 6 weeks of waiting for results, for a suspected Squamous Cell Carcinoma.

    I am just keen to get my tilt test out of the way and then to hopefully get some answers. Yes, I've got my Christmas shopping finished, but still have the wrapping to do. I'll need to post many of them this year, as we moved down south from Scotland earlier in the year - another additional expense! I hope that you manage to finish yours soon.

    Kind regards,

    Jolamine xx

  • Hi Jolamine, only just saw your reply, didn't seem to get a notification. I did speak to the breast care nurse, who was lovely. She said to ask tomorrow when I go for wound check in plastics department, to get a dr to check it for me as it's a reconstruction. She said if I can't get it checked there, they'll fit me into breast clinic for a follow up. She did also reassure me it's unlikely to be anything to worry about. With regards to venlafaxine, I have talked to receptionist at Dr's, who said someone will give me a call. I'm only on 37.5mg at the moment and want to increase it to 75mg, so hopefully they'll agree to that. Thanks for sharing your dosage, makes me think I won't have a problem. Radiotherapy therapy going well, just the journey is a bit of a pain, 3 1/2 hour round trip today, for a 15 minute appointment. Tomorrow I have to go for another wound check at a different hospital in the afternoon, so a tiring day. Hope you are feeling OK, your tilt test must be coming up soon isn't it?  Xx