My mum's journey so far

Hi I messaged a bit ago this is where we are at at the moment

Hi all I’m new to here,but at my wits end.

im Going to try and keep it  as short as possible,but sorry if I end up babbling.

my mum has copd,you will see why this is relavant.Fo quite some time she was unable to chew any meat ir swallow,had chronic heartburn and a funny shape at the front of her tummy,she is only 67.

my mum was sent for the camera down her throat in September,we waited and waited for results,I phoned hospitals,doctors only to be told no news is good news (WRONG) It has taken 3 months on the 14 December we were told my mum has pre cancerous cells,no one  knows why it took so long for the results.

In the 3 months we waited for results my mum had been admitted to hospital around 5 times for a week or 2 weeks including resus,as her sats were dropping all the time sometimes as low as 74.and that was only because I kept ringing an ambulance,each time she had to go through A&e sometimes on corridors for 12-14 hours,during these admissions she was asked if she has ever been told she had cancer,(ABSOLUTELY NOT) was her reply.

when we got the results in dec (pre cancerous) another biopsy was arranged for the 15th January (again still no results,as they want to send her for a pet scan first) pet  scan done on 2nd February (still no results) when we arrived back at my mums from the pet scan there was a letter there advising my mum that she had missed an appointment for arthritis and they have recently been notified that she has cancer of the oesophagus (SOMETHING WE HAVE NEVER FORMALLY BEEN TOLD) I have got the letter as we were told the pet scan results would be with is by the end of the week (last week) I presume now to see if it had spread anywhere else,my sister have decided not to break the devastating news until we have the pet scan results rather than have to tell her she has cancer of the oesophagus and again if it has spread anywhere else.

we do feel very let down,since the biopsy in September,some of my mums hospital admissions have been for chest infection,pneumonia even ecoli she was discharged from hospital with ecoli,resulting in a nurse calling at her home every day fir a week to put a drip up beside her bed for one hour then go.

Apart from that my mum has seen no doctors no nurses,she is in bed most days eating very little and sleeping a lot,it’s like she’s been forgotten about.

i do believe that the doctors knew this was cancer when they gave her the pre cancerous results in December as he was going off Septembers biopsy,although her discharge papers from hospital in December clearly as Carcinoma of the oesophagus (again this was from Septembers results as she had no other tests until 15th January.

Hopefully we will get answers soon then she can start to receive any treatment she needs.

Hopefully we might get the results from the pet scan tomorrow x

also there is no medical team or doctors or nurses looking after or even seen my mum

  • Hello Jackiem77, 

    Thank you for updating us about your mum's situation. What a stressful time it must be for you. 

    I do hope you get some answers very soon and that the treatment your mum needs can begin very soon. 

    How did the appointment go yesterday and did you get the PET scan results? 

    I hope you get some clarity about all this and that  you will get to chat to others here who may have been in a similar situation.

    Best wishes, 

    Lucie, Cancer Chat Moderator

  • hi we had our appointment with the specialist regarding the pet scan unfortunately he has now confirmed to my mum that it is cancer of the oesophagus,as she is unfit for surgery or chemotherapy,she now has an appointment to talk about starting radiotherapy In March.

    I had asked questions why it took 3 months to get the results obviously he has no idea but said he would definitely look into it,I must say he did say looking at her records there was a mistake,as initially whoever looked at the biopsy results from Septembers biopsy thought it was an infection.(which still doesn’t explain why it took 3 months especially with me calling both the hospital and her doctor to see if results were back)

    i did also ask if these results where given to us in a timely manner,and they had started the radiotherapy when it was at pre cancerous stage,he then stopped me and said we would not be sitting here now.

    this really angers me as my mum should of had a chance of radiotherapy,before this turned to full blown cancer. The main way to diagnose cancer is by biopsy,and the people that look at the tissue are supposed to be specialists in this.

    we will now see what our next journey brings