Good morning all , I haven't posted on here as yet but I monitor the site daily for tips and help etc.
I first felt back pain in January 2012 and thought it to be gym related , after 3 months my GP gave me anti inflamortory tablets,
These controlled the pain whilst we were away in Turkey and then Wales.
We returned from Wales at the end of August and all of a sudden I lost my appetite and began to feel quite sick.
The GP told me it was a sinus issue and gave me inhalers !!!!
Then after 3 weeks I had lost 2.5 stone in weight and I looked grey, the GP took a blood test in Sept , the same evening of the blood test I was called by the hospital and told not to take anymore tablets and to visit A&E in the morning.
I was then admitted to the haermotology ward that day and told I had MM.
I then spent 3 weeks in there on a drip…..
Now 9 months on I've had 6 months of tablet chemo , a stem cell harvest , and I'm due in hospital for the sct on Monday 10th of June , I'm told by the consultant I'm 95% MM clear but the sct is the only way to reduce this .
I've felt great over the last couple of months since the sct harvest even going back to the gym ( I never thought I would as I spent 3 months in a wheelchair due to foot drop, caused by the thalidomide ).
Thank you for your forum it's really helped