Hi to all

2 minute read time.

Last April I stood at the end of my son’s hospital bed staring stupidly at the junior doctor trying to figure out why he thought my son seeing an oncology specialist was a good idea, surely he would only want to see cancer patients … ohh!

Stage 4 sacral diffuse large B cell Non Hodgkins Lymphoma with bone marrow involvement. So the rollercoaster began.

At 2 in the morning he underwent an emergency laminectomy to remove pressure on his spinal nerves and prevent paralysis. With the NHL being so aggressive and advanced a regime of fortnightly treatments of R-CHOP was immediately started, even though the UK trial for this shorter cycle wasn’t yet completed. We were told my son couldn’t wait for those results.

A lumbar puncture to administer intrathecal methotrexate was also sandwiched between the R-CHOP treatments to stop the cancer spreading to the brain. Pneumonia and ICU were rough but my son fought for every breath and came back from the brink. After the chemo was finished four weeks of radiotherapy followed.

November 2009 brought the news we’d been hoping for – the cancer is in remission.

So why am I so depressed? Is there something wrong with me? I feel abandoned, resentful and isolated.

Everyone around us is so happy, life can go back to how it was and no one has to think about cancer any more. But life will never be the same for us and cancer is our companion.

My son turned 22 in September. He had to give up his studies and reluctantly move back in with his mum. He is adapting to the loss of feeling in his legs from damage to the nerves in his spine. He accepts waking up every day with a multitude of aches and pains and he copes with the weakness that overwhelms him without warning. Chemo brain and achingly cold feet are just a part of life.

Not once over the last year has he ever complained.

All of the medical staff told us to expect a long road to recovery and to take things as slowly as necessary.

But people around us are getting impatient, it’s almost 3 months since treatment ended and they think my son should be back to ‘normal’. Everyone has an opinion and some unwanted advice. I must make my son do this exercise or see that therapist. I should get him a blood test for this and give him supplements for that. He suffered from depression as a teenager so all his symptoms must be psychological. There are a multitude of websites that I really must visit and a million articles I absolutely have to read.

I am so grateful to everyone here who has shared their stories and experiences. I cannot tell you how much it helps knowing we are not alone and that there is support out there.

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Anonymous
  • FormerMember
    FormerMember

    What a lovely mum you are, he is ever so lucky to have you. Perhaps you feel so flat because you are simply drained and you have not had any chance to think of yourself for so long. Is there anyone who can just worry about you for a while? My mum and I cared for my dad and when we stopped we felt a lot of strange emotions, we are being really kind to ourselves (spa day was a very nice treat!) and we are gradually calming down. I am really pleased your son is recovering and I wish you all the luck for health and happiness in 2010

  • FormerMember
    FormerMember

    So glad to hear your brave son is in remission.  So many of our acquaintances, mostly well meaning, take the same attitude to my husband who is also in remission, in his case, from Mesothelioma.  Those who have never had a loved one suffering from terminal cancer do seem to confuse remission with cure.   After such debilitating treatment, it takes time to recover from the effects of chemo.  Remission also brings uncertainty for the future.  We fear that we will not strong enough to give the support we want to.  Those who truly care for us will try to understand, and support us carers.  The rest well…If nothing else, in this year I have certainly found who our true friends are.  Stay strong for your brave boy, but also try to take some time out for yourself.  You have been on a horrendous journey and you too need time to recover.

    Very best wishes to you and your son

    Daffie

  • FormerMember
    FormerMember

    Your story touched my heart.  My husband has cancer of the tongue, initially thought to have been caught early, but now apparently spread to his lymph nodes.

    Both you and your son sound amazing people - but why should you not feel angry, abandoned or resentful of people offering unwelcome 'advice'?  Whatever you feel is fine, as far as I am concerned.  I believe quite strongly that you can never step in the same river twice - I will never be the same again, though not always in a bad way eg because I had to take over all the long-distance and town driving that I used to leave to my husband, so I am now a much more confident driver than I have ever been before.  You also realise how fragile life is, and that cancer is not 'cured' but is in remission (and we are still a long way from that!).  

    Kindest wishes, and do keep in touch.  Cathy XXX

  • FormerMember
    FormerMember

    Really pleased that your son is in remission, you have both been through so much.  I am in remission from NHL myself, though with less treatment to cope with than your son, and really thankful for that but do find myself trying to find out what 'normal' is for me now, I know it's definitely not what I was before.  Once treatment had finished, after spending so much time at hospital and planning my life around chemo or radio sessions I was finished ... told take things slowly and start building your life again ... kind of felt like I was in limbo.  Close family are great but others around me like you mentioned expect me to be back to normal or my old self by now.  Would just say ignore the expectations of others, both of you take as long as you need and however you feel is OK.

    Love and best wishes,

    Jozzy x

  • FormerMember
    FormerMember

    Thank you so much for your lovely comments. Although I know it already, it is good to be reminded that it's ok however I feel and so good to hear feedback from such kind people who understand what we are dealing with.

    My son and I had the added complication of being made homeless in the middle of his treatment.  We were in temporary accommodation for a while before being told we had to go into a new property or be homeless again. We were given 4 days to move, it was christmas week, there was snow everywhere and my son was poorly. Slightly stressful.

    We now live miles from where we were so I have to find everything new from the GP to the shops and we know absolutely nobody in this area. Still, it feels like a new beginning, so maybe 2010 will be a better time for us.

    With best wishes and sincere gratitude to you all.

    Faith

    x