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Rachel50
Member
since
29-12-2018
29
Posts
8
Hugs
Thursday
I’m really not sure . I’m waiting for radiologists to give me a date. My oncologist said should know by end of this week and it will happen within a week. I was thinking needle biopsy. I have an extremely sensitive gagging reaction if anything goes near back of my throat so not sure what I’ll do if that’s what they decide. I’ll let you know as soon as I hear x thank you for your reply x
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a week ago
1 Hug
My recent scan has shown 16 lesions in my right lung.... add this to spine and liver mets it’s not been the best eleven months since my denovo diagnosis. Has anybody had a lung biopsy? Just looking for reassurance and any advice thanks
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02-08-2019
07:27
I have mets in my liver the pain is on the in breath shoots up my right side of back and through my shoulder blade. Hope things get easier for you soon x
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02-08-2019
07:14
Hi I am experiencing debilitating joint pain in my hips knees ankles and toes. I have liver mets, bone scan in February was clear. Think it’s a side effect from herceptin/perjeta. Any suggestions what may help? Thanks
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02-08-2019
07:12
1 Hug
Hi I have liver mets and liver pain. Does anyone take any supplements to specifically support their liver function? Thanks
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02-08-2019
07:09
1 Hug
Hopefully this option will be very successful for you. Sending love to you xx
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30-06-2019
01:05
Hi katzygirl I think you refer to mai7 ‘s information to my question. Thanks
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27-06-2019
06:48
Thank you my book arrived today so I’m sure once I get through it I’ll have questions. Think I’m going to research, talk to my oncologist and use both the medical approach I’m on combined with the COC protocol. I have lots to gain and not much too lose x I will look at the blogs thanks
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26-06-2019
09:30
Just keep trying to stop maybe get help from your GP. I’ve vaped since my diagnosis six months ago and have recently reduced the nicotine level. Don’t beat yourself up about it, just keep trying. We all have so much to deal with. Hope your treatment went ok x
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26-06-2019
03:41
Has anyone read Starve your Cancer book written by Jane McLelland. Advising use of prescribed drugs like metformin to starve the pathways cancer uses. I was diagnosed in dec last year then secondaries found two months later. Does anyone follow the protocol or use COC clinic in London thank you
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07-06-2019
06:13
1 Hug
Thank you for your replies. I’ve found them very supportive. I’m meeting with the palliative care consultant soon to discuss further pain strategies. I suppose I’m struggling with not knowing why I’m in pain, the tumours have shrank, my livers not enlarged. My oncologist has said it could be due to toxins with the dramatic reduction of tumours in a short space of time. I hope so with all my heart.
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05-06-2019
10:28
Hi everyone, I was initially diagnosed in dec 2018 with primary breast cancer, two months later I was told they had discovered one very large tumour and over twenty small ones in my liver. I started chemotherapy Fec-T, following my fourth cycle I started having stitch like pain in my liver area. This gradually got worse and I started taking morphine tablets 70mg twice a day and oramorph as top up. Following my fifth cycle I was in hospital with an infection for a fortnight . The decision was taken to stop chemo and continue with targeted therapy every three weeks. I have trastruzumab and pertuzumab. My first scan results were amazing 16 small tumours had vanished and my 55mm tumour has shrunk to 22mm. The scan showed my liver was not enlarged. Unfortunately the pain in my liver area continues, my oncologist doesn’t know why. Has anybody experienced anything like this, it’s a stitch like feeling, but worse. i also seem to be having terrible side effects from my treatment, flu like symptoms and pain so bad in the sacrum area of my back I can’t bend. Its been an overwhelming six months and any information on peoples experiences with liver mets would help x
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17-03-2019
05:40
Thank you
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12-03-2019
07:06
2 Hugs
I feel robbed I was diagnosed with primary breast cancer in December, ten and a half weeks later I’m told I have secondary in my liver. So no mastectomy just treatment every three weeks. Just so overwhelmed
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