Life after a SCT - A Survivor's Guide

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Let's see if we can collect some helpful information and real life experience that we can signpost folks to after they have come home from their Stem Cell Transplant.

A couple of useful things I found were:

My Consultant told me that going through treatments like these was like doing a boxing match and a marathon every day over the months of treatments and this was done without any training.

Think doing the London Marathon without any training and you had to finish it as your life depended on it……. this is the journey you have been on so it most likely will take much longer than you would think to get back to some normality - it took me a good 2 years and I was 60 at the start of my recuperation.

Yes some folks bounce back quickly post treatment but more than often folks take a considerable amount of time to recover.  6 months is the average recovery time…… at 3 months post my second SCT I was just out of my wheelchair and able to do a few steps with my walking sticks…. I was not able to feed myself due to my bad Peripheral Neuropathy and even then I was not eating much……. Your body has been through far more then you imagine so be kind to yourself, give yourself a break as you are doing good and honestly this will pass.

My consultant also gave me this basic scale for classifying where I was on the recover journey.

50% = when in the hospital going through the transplant process.

60% = significant medical/physical issues that do not allow any physical activity apart from a shower and short walk and not able to prepaid food. Reliant of others for preparation of food.

70% = Significant medical/physical issues that do not allow any specific physical activity (not including a shower) but short walks and making a pot of soup. Will nap after the task.

80% = Physical issues that limits you to one activity per day. (not including shower) Able to prepare some food for a couple of people but most likely still taking a nap after activities.

90% = Some physical issues remaining (weak legs etc) but able to do a few tasks and may not be fully fit for permanent work but could do part time work. May have to .take a nap after doing tasks or work.

100% = No physical after effects and able to do multiple tasks including being back to work.

She also said on average the recovery is about 6 months with your recovery improving about 10% per month post SCT

A web page by the Anthony Nolan Trust - The First year post SCT (link)

A web document by Dr Peter Harvey - Life after Treatment (link)

  • Good morning everyone.

    Just had some great news this morning, my 6 month post transplant biopsy shows all good and I am still in remission .

    A perfect start to Christmas xx

  • Great news Mark - great news........... I will have a wee dram tonight to celebrate I think.

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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  • 6 years ago today I had just received my very first bag of chemo starting my Magical Mystery Tour that would include 750 hours of chemo, 40 radiotherapy sessions and two Allo Stem Cell Transplants........ it was a long and bumpy road but I am now 3 Years 3 Months in remission from a condition that in 1999 I was told I would never see remission from....... keep pushing if you are just starting the SCT journey and if you are out the other end of SCT it’s not a sprint but a gentle recovery.

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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  • Hey guys. 
    Congratulations Parkrun Mark on the all clear at 6 months, perfect present to enable you to enjoy Christmas hopefully stress free. And Mike, 6 years ago when started chemo did you honestly for one minute think you’d be giving people advice on a forum now. Just shows why you should never stop believing. 

    Merry Christmas to all and may 2020 be a happy and healthy year for all of us. 
    Regards

    Mark x

  • So happy to see both Marks posting!

    a very Happy Christmas to all, and may 2020 be much better for each and every one.

    hugs xxx

    Moomy

  • Hi all and a Happy New Year. 
    daughter had a message from Lymphoma Action to say that her BBC Radio 4 Appeal broadcast raised £7,000 for the charity!

    hugs xxx

    Moomy

  • Hi Moomy,

    Thats great news and for a great cause, she must be pleased. 
    Hope everyone has had a good Christmas and New Year? 

    Regards

    Mark x

  • Daughter found it impossible to continue her solo tour of the USA, sadly; she totally lost her voice! She managed all her programme in Washington DC but had to cancel her other gigs, clinics and masterclasses and buy a new flight home. Thankfully her cold seems to be improving with plenty of rest, she has just about got her voice back, a delayed recovery as she simply had to continue trying to talk! She’s carefully taking her temp of course, always safe rather than sorry, even this far post allo.

    I was reminded by Facebook that it’s 4 years ago she and I sorted flights and somewhere to stay in Berlin to meet Thomas, her SC donor. That was truly one of the most emotional times of my whole life.

    Hugs xxx

    Moomy

  • Pants moomy, and as we often say, SCT the gift that keeps on giving. I do wish her a quick recovery.

    I have been surrounded by bugs for the past three months with ALL the family having something...... I have often thought I was coming down with something and looked at my emergency box of antibiotics but so far so good.

    I just got a letter in the week for my ‘Late Effects Clinic’ with my team.

    So lots of blood tests etc, the results are sent to Glasgow and the Late Effects Specialist Nurse will do a FaceTime with me........ four years post Allo number 2 ..... where is time going?

    There are parts of the SCT journey that will most likely never ever leave us and some things continue to mould our on going life xx

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

    Community Champion Badge

  • Hi Guys. 

    I can imagine just how emotional meeting your donor is as I sometimes get emotional just speaking about this person I know nothing about. 
    With regards to donors my sister-in-law was told last week she’s matched as a potential donor. She joined the register as a result of my situation so to know some good might come of my illness also made me a little emotional but also proud at the same time. Almost all my eligible family and friends have joined over the past year or so so hopefully more lives can be saved. 
    On a personal level I’m still having issues with GvHD but it’s manageable at present. I’ve been back at work full time since just before Christmas and I am living my normal social and family life. Big week coming up next week as I get the results from my recent MRI scan and first pet scan since my transplant in June. I won’t lie but I’m scared but fingers crossed I finally get a break. 
    Regards

    Mark x