SCLC: 7 years post treatment

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Hi

Several weeks ago I had my regular 6 monthly check up at The Christie and there is still no sign of the SCLC returning. As I have always said in these half yearly updates, that I have got this far post diagnosis has had very little to do with me but everything to do with the care, expertise and dedication of the medical professionals including initially  my GP and local hospital, and subsequently to date the ever wonderful The Christie hospital.

Those of us who have undertaken this journey and/or who have recently been diagnosed will have probably started with that one question in their minds; "How the hell am I going to get through this?". Unfortunately there is no standard answer as we all need to find a way to deal with it in our own way and on our own terms.  My personal attitude/approach was (and still is);

  • I am a great believer that my health is my responsibility, so therefore I felt it was also my responsibility to understand everything about the SCLC and the treatment plan. My most used words to the medical professionals during the diagnosis and treatment processes were "What, Where, When, Why and How". I am by nature a need to know kind of gal! 
  • Even though  my consultants provided me with full details of the treatment plan and possible side effects, I did Google everything which helped me to gain a broader understanding of what was direct cancer treatment and what was 'wellbeing' treatment (steroids etc).  I believe that by sticking to the reputable and regularly updated sites such as Cancer Research UK etc, it is easy to sort the wheat from the chaff, and there is a lot a chaff out there!
  • A combination of pragmatism and bloody minded stubbornness; I quickly learned which aspects of the treatment I could  control/negotiate and those where I just had to go with the flow.

The above approach will not be for everyone; as I said earlier this was/is my personal attitude/approach.

The main purpose of my 6 monthly updates is to provide a ray of hope for those recently diagnosed with SCLC and to show that it is no longer the automatic death sentence it once was.

Kegsy x

  • FormerMember
    FormerMember in reply to FormerMember

    The drain was the most bloody painful. But give it a few more days. I took arnica to help healing  just do little tiny walks no more than 20 steps at a time  little and often if you can hopefully drain out soon and that will make do much difference to pain levels  xxxxx

  • FormerMember
    FormerMember in reply to FormerMember

    Thanks looking forward to drain out

  • FormerMember
    FormerMember in reply to FormerMember

    Hi all..anyone know if symptoms get worse just before your next chemo is due..feeling pretty rough before tomorrow's cycle..?  

  • FormerMember
    FormerMember in reply to Kegsy

    Hi I would be happy to just don’t know how! Please help 

  • FormerMember
    FormerMember in reply to FormerMember

    Hi how are you haven’t heard from you in a while. 

    Janet 

  • Hi Kegsy,

    You might remember me posting before about my friend. She is limited, chemo and radio with PCI finished last August. Last scanned in Jan, no changes, tumour had shrunk right back after about 3 chemos.

    She has not really had too many days where she feels "well", and the oncologist has always said that it is down to the amount of treatment she had. Not sure if they gave her stronger as she is only 46.

    Of course, every ache pain and twinge is a worry, but just recently she has a pain in her side, near where it all started. She is due another scan in 2 weeks, but I was just wondering do you ever get any pains at the original site or any other unexplained symptoms?

    Thanks a lot

  • Hi 

    Of course I remember your posts.

    Everyone recovers at their own pace, so don't worry too much that her recovery is quite slow. 

    Yes I think we all get the odd twinge or ache at the original site of the cancer. I always put this down to the scar tissue and possible nerve damage/sensitivity left behind by the radiotherapy. Mine is more noticeable if I have been more active than usual.

    The forthcoming scan will hopefully reveal nothing sinister and she can then get on with her recovery. She will have to work at the recovery; it doesn't just happen.

    I hope this helps.

    Kegsy x

    "If you are going through hell, keep going" ; Sir Winston Churchill
    " Cancer may take my life; however it will not become my life" Kegsy August 2011
  • Thank you for your kind words... Her oncologist said that it normally comes back in the first 1-2 years, obviously could be longer.

    She is 14 months in since diagnosis , gets a lot of these pains and aches. Once it was lack of vitamin D, they always tell her its just the treatment. Also she has a 7 year old to look after, so not much resting goes on!

    Still, I'm very very nervous for the next scan and results.

    Hope you're ok

    xx

  • Hi

    Yes I am well.

    Just a thought but perhaps she needs to have a word with her GP about having a bone density scan, especially as she has already had a vitamin D deficiency. The high dose radiotherapy that was part of my treatment weakened my bones, not enough to be classed as Osteoporosis  but its lesser version of Osteopenia.  I now have a bone scan every two years to check my bone density is improving. It was my cancer team who first noticed the bone issue on a CT scan and advised me to request the bone density scan via my GP.

    Fingers crossed for the forthcoming scan.

    Kegsy x

    "If you are going through hell, keep going" ; Sir Winston Churchill
    " Cancer may take my life; however it will not become my life" Kegsy August 2011
  • Sure, i will be going with her to the next appointment so will ask thanks.

    She had blood tests 2 weeks ago and her scan was already booked in for late June. Do you think they would call her in sooner if the bloods showed anything?

    I'm getting so worried...

    xxx