August 2019
1 Kudo
Hi debbru, Let your doc know about the rash. Make sure to moisturise your skin & wear sun protection. Here is a link to a web site that gives alot of info on Herceptin. It might be useful to you. https://www.cancerresearchuk.org/about-cancer/cancer-in-general/treatment/cancer-drugs/drugs/trastuzumab Budgie
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August 2019
2 Kudos
Hi there Cat, I understand exactly what you mean. You do tend to feel that way with some oncologists. When I was going to Peter Mac, they even have a machine where you scan your letter with your appointment date & time, it spits out a ticket for you which tells you where to go. Then you sit & wait till your number lights up & you can go to the doctors room. No personal contact at all. Then to have an onc that just doesn't care is like adding insult to injury. I hated that place, it just felt like an abattoir. Alot of people don't know that your GP can refer you to a radiation onc as well. My GP in Canberra did just that for me, as my onc was playing the "wait & see" game, & I wasn't happy with that. He'd played that game with me once before & I ended up with a fast growing bone met in my jaw which left me with a nice big hole in it. So don't be afraid to use your GP. If the radio onc doesn't think you need any treatment from them, then at least you have it straight from the horse's mouth. Budgie
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August 2019
2 Kudos
Hi Claire, So sorry for my late reply. I've just had an absolutely mad weekend with a full house. One of my daughters & her family, plus one of my sons came to visit. My daughter has 4 children, so it was a very loud, hectic house - absolutely fabulous! How have you been lately? Healing up nicely, I hope. I am trying to make a wedding gift for my other son & his wife out of the quilling, but it's taking so much longer than I had hoped. I'm a bit of a perfectionist, so if I'm not happy with something I have to do it again, but this is taking so long to get right. Anyway, I'll get there, eventually. My attempts at flower making so far I was in awe of my mother when she would knit. It was amazing to watch her reading a book or watch TV while she knitted a jumper or something. Fabulous. Cheers Budgie
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August 2019
2 Kudos
Hi trish57, Don't be sad. It doesn't help anything being sad. Your family may not know what to say to you without upsetting you. I used to update my siblings with progress reports every now & then, but I stopped doing it because I was getting no response from them. It's not because they don't care - I know they care. They just don't want to think about me dying. They don't know how to talk about it. It's a good thing that you met with a counsellor, & certainly nothing to be ashamed of. Everyone needs someone to talk to. I don't know anything about Non Hodgkins Lymphoma. Would you mind telling me what it is? Budgie
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August 2019
1 Kudo
Hi JR, It sounds like your husband is feeling very sorry for himself & taking it out on you. Or, he might think he'll be protecting you from the hurt if he pushes you away. Then again, from what I've read from other caregivers, it could be a side effect of the chemo he is on. If that's the case, he may not realise just how badly he is treating you. Whatever the reason for his behaviour, it should be stopped. Maybe he will need a threat of you leaving him to jolt him out of his abusive ways. Would he be open to counseling? I'm sorry I can't help you JR. It's a horrible situation to be in. Budgie
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August 2019
2 Kudos
Good morning Claire, The drug I'm on now is the only one left for me to try as I've been thru all the others for kidney cancer. So when this one stops working things will just progress naturally. I'm fine with that, I've had a happy life, with a wonderful family I'm very proud of. I'm happy talking about it. Death is a part of the whole cycle of things. We move around alot as my hubby is in the defence force, so I have quite a few acquaintances, but I too, like being alone. My day entails doing what house chores I can, then im either doing puzzles or cross stitch. Lately, I've been trying my hand at paper quilling, with rather limited success. Practice makes perfect though, right? And while I've still got time, I'll keep trying. Have a good day. Budgie
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August 2019
1 Kudo
Hi Claire, Not rude at all 😊. I know how small comments can get lost in a thread very easily. My nickname isn't very exciting, just a play on my maiden name, which I'd rather not say 😉. I was diagnosed with stage 4 kidney cancer back in Aug 2012, on oral chemo (6 different drugs so far - the current one being the last available treatment for me) ever since. Just plodding along, taking each day as it comes. I hope you are feeling well after your surgery. Budgie @Lehiatus wrote: Hi Budgie, I realised I haven’t reached out and said hi! How rude! The banter here is a great surprise to me too, I wasn’t sure what I’d find when I signed up but it’s been endless relief to find people battling similar issues and just knowing I’m not going mad. Tell me a bit about yourself- where did your nickname come from? Cheers Claire
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August 2019
2 Kudos
Hi trish57, Welcome aboard. Do you mind if I ask what you've been diagnosed with? Cancer is an awful illness, & would be absolutely horrible to go thru it alone. I am very sorry you have no one physically with you to share this burden, but you will have plenty of people on this site who can offer advice & a cheery word. 😊 Budgie
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August 2019
2 Kudos
I'm already nuts, & it's driving me insane! It's called chemo brain. I tell you, it's so frustrating when you're trying to think of the word you want to say & it just won't come. Or the words just come out completely the wrong way around. Mind you, what eventually comes out can be quite funny .
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August 2019
3 Kudos
Hi Claire, I am sorry for hijacking your thread 😉. I must say that I have been thoroughly enjoying the banter between you all. Keep it up. I hope you are recovering well. All the best. Budgie
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