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.
There are sign everywhere in my local Heamatology ward and clinic saying a week in bed is like ageing physically by 10 years
My consultant gave me this basic percentage 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 prepare 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 recovery time-line is about 6 months with your recovery improving about 10-15% per month post SCT
This is an average time-line….. with general acceptance that when in the hospital going through the SCT process we are physically at about 50%…… any less would indicated some comorbidity issues like pre-existing health conditions that may reduce the 50% starting point and possibly add a month or so onto the recovery end…..
For example I have Asbestosis so this was looked at very closely and due to my prognosis was seen as an accepted comorbidity…… so I went back a good 10%…… other issues could be blood cancer type specifics, genetics…..
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)
Great news Mark - great news........... I will have a wee dram tonight to celebrate I think.
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.
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
