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)
Yes it’s all a bit on the crazy side but unfortunately not unexpected.
Sadly very true, Mike. Hope your area isn’t suffering lockdowns? (I didn’t think so but we don’t always get full news of them, after all?)
just found a you tube interview that daughter did for a South American Trombone group, it was late at night for her so she didn’t look her best, but it was an excellent interview!
hugs xxx
Moomy
Last Monday we were put under an across Scotland - no one in your home only in a garden and even then from one household up to a maximum of 6 people...... so we ordered a patio heater yesterday and sail awning...... Christmas dinner outside
I will have a look on YouTube
Good idea, Mike! Just hope the weather plays ball then!
Hugs xxx
Moomy
I’m not sure if any or all post SCT patients would be able to have the Covid vaccination, but I just saw this in BBC News (hope it posts) and it seems good news!
Covid: Jab for people who cannot be vaccinated trialled https://www.bbc.co.uk/news/health-55022288
Hugs xxx
Moomy
Time will tell on this one moomy, there are a few of the vaccines ‘play’ around with the T Cells..... maybe not a good combination when I had a T-Cell Lymphoma
Just heard a questions and answers on Radio 4 and apparently immuno compromised people will be able to have them as they are not live vaccines
My team are firmly on the fence with regards to me and my type of NHL - time will tell
That sounds positive parkrun mark. I will get one unless the consultants are a really against it as I like to travel and airlines like Quantas are already putting the comments out there of no vaccination no travel on the airlines. I had the MMR which is a live vaccine and that was fine.
Paul
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