Looking for info

Basically, this is about my Dad, who is 67 and was diagnosed with mesothelioma on August 24th 2017. Since then, with the combination of the cancer and now chemo he has lost more or less 4 stone. The chemo is hitting him hard, there have been times where he cant even drink let alone eat and the sickness has been horrendous (they have been back and forth and are trying different anti sickness meds). He has become so weak and tired. There are times just walking from the livingroom to the kitchen tires him. He's just sitting on the sofa all day.

Is there any help at all...or has anyone any suggestions? I know there's not much I can do but watching him go down hill so quickly has been a shock. They never really told how bad it was at the start....he went to Papworth about an op trial they do but they said he wasnt suitable but never actually said why.....it feels like they keep him the dark.

  • Hi samsunguk, 

    I'm sorry to read about the impact your dad's cancer and the chemo is having on him at the moment.

    I know you're looking for advice on how you can help him at this time so I just wanted to put you back in touch with [@jules54]‍ as I think she may be able to help you at this time.

    I wanted to give you our cancer nurses telephone number in case you wanted to chat to them about this as well. Their freephone number is 0808 800 4040 and are available Monday - Friday (except bank holidays) between 9a.m - 5p.m.

    Kind regards, 

    Steph, Cancer Chat Moderator

  • Hi samsunguk

    This is such a difficult journey for you and your Dad plus extended family.  The affects of the chemo can be extremely harsh on the body and my hubby was at his lowest ebb during this treatment too.  Ways to help are sadly somewhat limited and I found it frightening and frustrating that I was somewhat sidelined.  My hubby did not want company, sympathy but merely peace and quiet to let him deal with it as best he could. Inevitably he was restricted to be indoors during the worst of the sickness and like your Dad had tried endless different anti sickness treatments all to no avail.  His body just rebelled against the chemo and half way through his planned course the decision had to be taken to end palliative chemo as it was taking away his quality of life.  We were extremely lucky that his consultant explained everything from the start of his diagnosis and we welcomed the frankness though it is not the news you wish to face.

    Once my hubby was off chemo the sickness abated and though he never regained the weight lost he was able to cope for the remainder of his journey with mesothelioma.  As to the eating and drinking the chemo affected his taste buds and he just did not enjoy all his old favourite foods so we found, by process of elimination, those he could enjoy and stuck to those plus prescription milkshake supplements.  We had a his and hers fridge and he was never without a bowl of chocolates/sweets by his side as  this was his 'heaven' and one he took advantage of. To the  grandchildren (then just 5 and 1) he became the grandad with treats (he had a large wicker tea cup which was filled regularly with fujn size bars and healthy bites).  Looking back I can now be grateful that he was given some extra time with us because of the chemo treatment but watching those down days was heartbreaking and the journey with him declining day by day so sad. 

    I do not know why your Dad was declined for the trial other than perhaps his body could not meet the required criteria but perhaps he could ask at his next consultation.  My hubby never had the offer of other options.

    This forum is a great source of support even if you just want to write your own frustrations down, all of which are perfectly natural.  So many emotions attached to a cancer diagnosis/journey and it affects all the family.  Happy to chat if you wish to post again.  Jules54

  • Thank you Jules - I know this reply has been a long time coming but I thoroughly appreciated the times you have replied to me.

    My Dad kept going down hill and he died in hospital last Sunday morning at 2.45am - he was admitted to hospital via A&E about 23 hours earlier and we all stayed with him till the end.

    There were several things that came out while we were there. They had to find Dad a private room and we ended up on a random ward and one of the doctors on that ward said that after looking at his last CT scan that he had hardly any area left on his left lung to breathe so he was restricted to only his right side. This wrangled me like hell because I was there with my Dad and his wife when his palliative care doctor told us that it had progressed but not once did he tell us that his left side was that bad.

    I realise going on about it isnt going to change the outcome....I'm just pee'd off and feel a bit sceptical about doctors now.

  • Hi

    Just returned from a few days away and would like to extend my condolences after reading your latest post about the recent death of your Dad.  I am sure it is all feeling very raw right now and hope you have support close to hand during the comings weeks/months.  Of course you are correct when  you say nothing can now change the outcome but that does  not stop the hurt and anger bubbling up inside and I am sure many of us would have preferred the hindsight of knowledge during our loved one's illness. My hubby preferred to 'protect us' from everything he found out and it was only my 'badgering him' that  led to my fully understanding and thus accepting his point of view. I was very fortunate that his doctor agreed to talk with my afterwards and help me through my grieving process. 

    Take care of yourself.  Jules