Oesophageal, spread to liver, metastasis

Vicky

i know how scary it seems and that word Caner means a death sentence. do you have a team with you yet or had your MTD meeting 

Chemo can be very scary I know I broke down when mine started but the nurses are there to help you and give you good advice  . Your family will be a great support to you don't be afraid to talk to them all the way on this journey . They will be on this ride with you and of course use this forum a lot of people been through the same and very journay is and will be different.

i know its hard now STAY STRONG  XX  

Every journey 

I know how your feeling  x I'm just on my for my first chemo session  x   keep your chin up .x 

Hi Vicky

I'm so sorry you're on this journey thst really no one wants to be on. I had my first round of FLOT at thend of September 2022 and all I felt was highly anxious. The treatment was not easy but my son was my guiding light. I focused on him and watching him grow up that got me through the darkest of days. What is your treatment plan? There are a number of supports out there- various charities around cancer and of course Macmillan.  This forum certainly provides support for all of us. 

Take care

Yes it’s all moving fast

within 2 weeks the Mtd meeting 

diagnosis last Wednesday, oncology app yesterday and chemo and blood transfusion Friday 

thank you for Your words Nic nac 

Chemo and blood transfusions Friday 

6months of chemo 

and tablets 2x a day 

I hope it goes well 

Thank you.  Not a good start though  my appointment  letter says 10 o'clock  but on there list it's 11.30  . These things happen  x 

All the best Vicky.

I'm 40 with the same diagnosis including mets to liver. I finished 6 cycles of CAPOX in April.

If you are on the same regimen, then it is tough but focus on the extra time its hopefully giving you. That and my 5 and 1 year old kept me going.

Ahhh bless you, sending positive energy