Hi all, not posted for a while. I am now 17 months post sct for myeloma and been told I am still in remission.even though I still have bone pain and still struggle to walk for any distance recently had MRI scans on spine and hips they now tell me I have early stages of arthritis in both hips, prolapse discs in spine and degenerative bone disorder which none of these were picked up on prior to stc.also just been told I am diabetic and now have liver disease.has anybody else had similar problems post SCT. I would be grateful for any advice, thanx in advance.
Hi again Little G the problem post SCT is differentiating between ‘left over’ issues because of the SCT process and other medical issues that may well happen anyway…. SCT or not
I can only refer to my post life after having 2 Allo (donor) SCTs
More specifically after my sr ind Allo SCT in Oct 2025….. I am left with heart problems due to a reaction to the Melphlan so initially A-Fib on and off for between Oct 2015 and April 2022 when I had a heart attack….. but a few stents later and I was back on my feet and doing good.
I put some weight in over the 2 years after Allo number 2 so a blood test indicated that I was pre-diabetic but a change in diet helped to take me back from the diabetes cliff edge.
Even 8+ years out I have regular chest infections but my trusty on the shelf antibiotics catches these before they develop…. although over the past 8 years I have been 5 times back in hospital (32 days) with Chest Infections, Lung Fungal Infections, the RSV Virus, Pneumonia x2 and Neutropenic Sepsis x2.
I often have kidney infections but this is often my fault as at times I don’t drink enough water.
Amazingly my Spinal Osteoarthritis (first diagnosed in 2010) has disappeared and I am no longer in meds for this.
Thanks for the info Mike, sounds like you've definitely been through it yourself and still battling, not to sure I can do the same
Hi all just joined ,just starting my second week of treatment so still not sure what to fully expect from meds. Time will tell.
Back in late 2013 I was told that Allo SCT had to work….. if it didn’t I would only have a few years on palliative care…… so I am living the dream.
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