I have been living in Australia, Sydney, for the past 9 years. In February 2005 I was diagnosed with multiple myeloma and am at present free of medication having been successful on Velcade (bortezomib).
I would like to know where I could be serviced in terms of hospitals somewhere in the south west or the midlands, having lived in those areas for 25 years and have connections there, family and friends.
I am thinking of returning in April May of next year. I would also need to know what help I could expect to receive in terms of support.
I am a British citizen.
Thanking you,
Yours sincerely,
Colleen Berg
Forums
Re: Myeloma centers in Southwest or Midlands of UK?
Hi colleen,
I believe the QE is an option to consider, but I'm no expert. I'm at the Royal Marsden in Surrey which has Gareth Morgan.
Good luck with your return to the UK,
Debs x
I believe the QE is an option to consider, but I'm no expert. I'm at the Royal Marsden in Surrey which has Gareth Morgan.
Good luck with your return to the UK,
Debs x
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hopefulmum - Name: Deb
- Who do you know with myeloma?: Myself other patients
- When were you/they diagnosed?: July 2009 with smoldering Myeloma
- Age at diagnosis: 34
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