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)
Hi Moomy,
Good to hear your daughter is doing well this winter, long may it continue. 7.5 years certainly is a very long time but I suspect it speaks volumes for her determination.
I was just popping in anyway to wish everyone a Merry Christmas and a happy and hopefully healthy 2019.
Best Wishes
Mark x
Good to hear this news moomy and let's look for this to continue and so good to hear from you Mark I do hope you are doing well.
So an great chance to wish everyone looking into, going through and those who have come out the other end of Stem Cell Transplant a very happy Christmas and let's look for 2019 to bring health and happiness all round.
I’m all good Mike thank you, just getting on with things. Still having Nivolumab and I am due to have a scan on the 3rd Jan so will know then if it’s worked or not. Feeling ok and still working, running etc and even still training for my half marathon so just enjoying life at the moment and making the most of it, I know the battle is still to come. They wanted to scan me just before Christmas but I said no as if it’s bad news it can wait until the new year, I will worry about it then.
I will let you know how my scan goes but in the meantime I hope you have a wonderful festive period surrounded by the people you love.
Regards
Mark x
Great plan Mark and have a great family time.
I didn’t cross my fingers firmly enough! Daughter had come down with a cold, but we hope it will be fought off by her somewhat improved immune system with I/G’s
she began on Saturday, aware when she was doing the Tina Turner double shows (matinee and evening) that she was feeling pretty awful, so has ensured she has a thermometer with her and is regularly checking. She’s at her housemate’s family for a couple of days and is resting plenty!
Christmas hugs to all xxx
Moomy
Fingers crossed as well x
Thought I would bump this thread as some folks will find the information useful and others can add to it.
The picture below is taken in my local hospital General Admissions Ward (when I was in last week)
It highlights the reality about getting out of our beds and keeping going regardless as to how hard that may be.
It's so important to keep moving, I used to walk the length of the ward drips and all. I'm sure this help me regain my fitness. It's a long journey back to fitness. But it is important to keep pushing forward. Check up tomorrow almost 18 months on . Mike the trip on the QM2 from NY was amazing worth the stress of booking and oops 3 kilo on !
suexx
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