Hello, I am feeling a bit speechless following being told two days ago that my "only very slightly" swollen pelvic lymph node - which an MRI scan a few weeks ago revealed is cancer - is incurable. This is due to the fact that because of the "very aggressive" course of chemo and radiotherapy and brachytherapy I went through last summer 2023 the surgeon has said he would not undertake surgery to the lymph node as it would likely cut into my bowel.
I had been told last month that if not surgery they would be giving me more radiotherapy abut two days ago was told they have now discussed this and the doses of radiotherapy I have already had last year were so high that I cannot have any more as it would be harmful to me. My cancer diagnosis in January 2023 was stage 4 cervical cancer: I was told I had a year to live if I didn't undergo the treatment which they said would be "radical" but the aim was curative. I was told it had also spread to the pelvic lymph nodes. In December 2023 I was told it had all completely cleared. Following several scans this year I was told the pelvic lymph node is showing slightly, only by 2 millimetres - but that it should not be - and finally they have discovered it is cancer.
Two days ago the consultant said they are "going to watch it" and he will see me in 10 weeks time after another MRI scan which will tell them if it has grown or spread. All I know at the moment is that it might have grown a little bit by then - or it could grow a lot. If the latter, he said the plan will be to give me more chemotherapy plus immunotherapy - but that it will not be curative.
It is now hitting me that I have incurable cancer with no idea how long I can expect to live or how ill and in pain or sick and exhausted I will be, whether I will again lose my intellectual faculties as well as how bad I can expect (will it be for ever until I die?) the gastric and bowel effects to be. I wonder if anyone here can relate to this at all - I had hoped to go back to my artwork and writing publicly as well as further study but as I am already 74 this is now looking uncertain if not unlikely.
Hi Minmax
Thank you very much for your words of encouragement and information. What a shock to be told your cancer has spread to your liver and lungs and neck, I cannot imagine it, it makes me feel possibly lucky - but having said that after reading so many testimonies my knowledge is jumping quickly from nil to going up and up the ladder of awareness - so getting prepared for any scenario. Amazing to hear a near impossible operation was carried out 11 years ago and still cancer free. Also encouraging to hear you have not got many side effects at the moment. I am learning that we are all so different and that there are endless variations of diagnoses, treatments and long-term effects and outcomes. So yes I do have hope. I have just booked myself a theatre ticket for Warhorse at end of November - so should be just after seeing the consultant and getting the updated diagnosis and plan - if he keeps to his promised appointment schedule. I booked a really good seat as I have always wanted to see it and I think I have only ever been to the theatre about three times - it is giving me an an enormous boost to look forward to it and is a huge counteraction to everything going on.
Thanks again
Oldsalt
Hello Codfish
Thank you so much for your very helpful reply. I should firstly correct my original statement in that I have remembered my cervical cancer was 3C1, not 4 - so perhaps that makes some difference as to how much it is in the blood. I am very grateful for your explanation about chemo not likely to be as bad as before and about the aim of treatments being to reduce symptoms and maintain quality of life - as I have been more upset at the prospect of feeling dreadful again and unable to function than I have been about dying! Also your encouragement about being able to get back to my artwork and writing as I am experiencing a huge jump in being able to focus and make decisions about going forward in that world.
I m glad to hear the side effects for your recent chemo are less than previously and that you are in remission.
Thank you, your details are very encouraging and hopeful
Oldsalt
Hi Oldsalt, It is a bit of a rollercoaster at first but I am sure you will get your head round it soon. We have all been there and you are right to take things slowly to start with and gather all the information you can before you decide to do anything! Please let us know how you are doing. Take care
Love Annette x
OldSalt It is so easy to jump to unfounded conclusions about treatments etc . The fact of the matter is we are being poisoned and they can only give guidelines on the type of side effects one may get. We are all different and hence react differently and to treatment. I had a weird one where it felt like a had a phone vibrating in different parts of my body. Told it was nothing to do with my treatment then told it was barber chair syndrome , Happy days it went, I was told I had a heart attack and had a stent fitted , Now apparently there is no sign of a heart attack . Tumours are on hold at the moment and I will deal with whatever when it arrives and take any treatment offered. They said to me in February they usually wouldn't offer treatment so I am very grateful . Think positive I say All the Best Minmax
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