Mums secondary brain cancer

Hello , I'm new here and just needed somewhere to express the sadness and hurt I'm feeling. 
My mum was treated for lung cancer a year and half ago - by removing a large part of her lung . It was a big operation and took a long recovery to get somewhat back to herself again , however it was a success and a big relief for us all. Her mother died of lung cancer at a similar age so the original diagnosis seemed like an instant death sentence. So to have had the cancer removed successfully, without chemo or radiation  - Was just amazing news . 

However , mum started to get ill again and was due to have her chest re scanned to check anyway to check the cancer had not come back . Unfortunately they found it had developed in the lymph node in her chest. She was put on an intense course of radiation/chemo and this was with intent to cure . It made her so very poorly and weak . She became even more bed bound, and with COVID restrictions I had been unable to see her or support her . Its just her and dad . 

She had another scan recently and the follow up from that was good news , they had shrunk it enough and we're just going to monitor her over the coming months. 
 A sigh of relief again for us as a family ! Although she is still weak and unwell and not herself

Fast forward a couple more weeks and she has a big fall, as she explain her legs gave way . It happened a couple of times and she did a lot of damage to her back and hip (she has osteoporosis) so much so she is now unable to stand up or do anything for herself.  Taken into hospital and scans on her brain show lesions which is what's causing her unsteadyness. 
 

It's clear she has lost her battle, she is 58. I am 30 with a new baby and I'm just so devastated for her and me and my family . I'm currently waiting for the prognosis of this , but we already know it's not good. The idea of being given a time frame of life when so much has already been spent fighting already, I just feel so sad. I have missed being able to be there for her , and even now I can't be and it's so painful . We had so many plans to do the things she loved "once she wins her battle again " I just can't imagine her being gone. 
 

I'm in shock , we all are . I wish I could take her pain away . 

Any advice on dealing with such news ? And in a situation where I can't physically be there for her :( I'm already grieving and she's not gone yet . I think I'm grieving the loss of the independent strong mum I've known and the loss of memories we can no longer make.


 

  • Hi Eagleb

    I am so sorry to hear about your mum's news, the love you have for her really shows through your message. I completely understand that added covid restrictions and not being able to be there for her adds another level of devastation to this already horrible, horrible time.

    My mum was given a few days to live, and I already started grieving her whilst she was here with me, but the couple of pieces of advice I would give you are please wait for the prognosis from the consultants, otherwise your mind takes you to really dark places and this won't help you as everyones case is so, so different. There could well be other things to try but until you actually speak to them,  you don't know for sure. 

    The second part is that try to make the most of the time you have with your beautiful mum. My mum was taken into a hospice a few days ago, we all had a covid test and we have been able to spend those moments with her, managed to say everything we have to say to her and it brings very little positive news to what we will face without her being here, but at least we are able to do that. 

    I wish you lots of strength waiting for the full prognosis, and I genuinely hope they are able to help your mum. Take care of yourself XX

     

  • Thank you [@Newlife101]‍ 

    i am sorry you was only given days :( it's so cruel. It's nice to hear you was able to spend her last bit of time by her side . Every family deserves to be able to say goodbye . I'm so sorry for your loss. 
     

    The docs had spoken to mum and dad yesterday and said they can't say how many months she may get but there's a chance a heart attack could happen before. My dad had to sign a do not resuscitate yesterday as mums body wouldn't cope. It's so unnerving thinking at anytime she could be gone but at the same time she could be here a little while yet . I hold hope I can spend time with her when restrictions ease. I am grateful for being able to FaceTime daily , she's still very much my mum and she is brave , braver than all of us. 
     

    My fear is for her to deteriorate before us all and we lose her before we actually lose her if that makes sense . But at the same time I want her with us as long as possible . 
     

    she has the consultant tomorrow with a plan for going forward, not sure they may offer some radiation. I just don't want her to have added pain if it isn't likely to make much difference. 
     

    She's always such a positive and mellow person , If there's one thing I can learn from her and this , is to take things as they come and make the most of how precious life is. I feel sad my son won't know her at all but I am grateful she was able to meet him a couple of times before lockdown. 
     

    thank you for your advice. I will continue to phone her regularly and make every conversation count xx

  • I'm so sorry to hear about the most recent update, it's so hard to hear. Hopefully with the update tomorrow they can give some positive news to you and your family.

    Your mum sounds like a fighter, so even though she's unwell, people have an unexpected way of rallieying themselves when they still have things to live for. I'm sure your mum cannot wait until she's allowed to be with you again. 

    Keepinf everything I have crossed for your mum's update tomorrow, let me know how you get on.

    Sending so much love to you xx

     

  • Thank you [@kate2021]‍ for your kind reply. I have spoken to my dad and it looks like she will need a hospital bed at home and lots of adjustments being made at home ready for her to be discharged hopefully by the weekend. 

    I have started receiving messages from close family and friends, with the love and sorrys. It makes it a lot more daunting all of a sudden. 
     

    I find it very helpful to have come across this forum. It seems to be a common thing to have the sadness come in waves. One minute I'm positive and the next I'm a nervous wreck , I feel a sense of panic that I can only describe as being a child and losing your mum in a crowd or supermarket. Except now I'm an adult and the fear is so much worse. Times in life when I'm sad or worried I always have my mum to speak to except now I can't burden her with all this emotion. 

    Hopefully they can have some suggestion tomorrow to help her - without too much side effects. It's a hard one. I don't want her to waste any time she has feeling more rough. 

    Thanks again for reading and replying. It's nice to be able to just type away sometimes. 
    xx
     

     

     

  • A tip for you with equipment at home, make sure that your dad asks the occupational therapist who is issuing it, to run through everything before her discharge. My mum was unfortunately In a similar position and my dad was left a little overwhelmed of what to use, when etc. A good OT should do this anyway!

    I agree it is nice to chat to people here, it feels like you're in a group that understand what you're going through, which unless you have experienced it, it can sometimes be hard to offer support.

    I really hope the consultants have some good suggestions too. Take care of yourself too, I know the appointment waiting can feel a bit overwhelming with all the emotions running everywhere xxx

     

     

     

  • Thank you for your advice - everything has been arranged for her discharge (which is now today). She has had everything put in place by the OT, including a hospital bed. 
     

    The lastest is that it's just about her end of life care now they don't want to put her through radiotherapy, and I think the selfish part of me is slightly angry about it but as I'm coming to terms with things I am more concerned with her quality of life now and I agree it's in her interest. 

    She is in good spirits , I have got her a photo memory blanket made (got the idea from these forums) and I don't want her days to be filled with seeing us sad . We do not know how many days /weeks/months we have , so every day is a blessing. 
     

    Id do anything to go back and have one more holiday with her to our favourite place . I am so grateful I have many videos and photos as memories.

    xx

  • I'm happy to hear your mum is being discharged today, I hope you manage to spend some quality time with her v.soon! 

    You sound very brave, and she will be so, so proud of you for that. I think the last thing my mum wanted to see was us crying around her, she wanted to enjoy every precious moment we had together. ️

    If you need to chat about anything, I'm here, anytime xxx

  • It's the worst pain isnt it. It almost doesn't feel real. It's actually 12 years this year I lost my mum to small cell lung cancer. She beat breast cancer , only for the lung cancer took her life. I'm actually back in the night mare , this time it's my big sister, she had breast cancer , it spread too her brain. She has many tumours and nothing can be done.  She has a hospital bed at home and is receiving hospice palliative care. She was the most positive person I know up until a few weeks ago. Until they said theres nothing can be done. She has 3 kids has a baby granddaughter.  It's so sad. And too everyone who's going through similar stories , lots of hugs to you all. Just take a day at a time. Sometimes just an hour at a time