Hi, just a quick note to say the meds have put me into remission now – about 3 months now. Hoping it will last! I still have to keep taking the pills, but we are experimenting with cutting the steroids which give me grief. I will write more soon to maybe say more on how the treatment is going, for the benefit of other myeloma patients. Hope you all have a good summer!
Aciclovir acid relux Acyclovir Adcal Alendronic Acid Allpurinol anti-emetics antibiotics bloating Bonefos bone marrow biopsies Bone marrow test c.difficile chicken pox virus circulation booster Clexane clinical psychologist CTD Difflam DVT Endoscopy ESHAP chemo excess body hair Gabapentin hiatus hernia Hickman Line hypercalcaemia Imipramine itching Lactulose Leicester Royal Infirmary light chains low blood pressure magnesium magnesium tablets Myeloma Beacon nausea nerve contractions nerve damage neutraphils NHS 'Reform' NHS Reform Bill Nystan paraprotein peripheral neuropathy pink cheeks plasma cells platelets post-herpetic neuralgia potassium Ranitidine rash red cheeks remission removal of Hickman Line retirement Revlimid shingles spores stem cell collection stem cell recovery stem cells stem cell transplant steroids steroid side effects stomach cramps Sudocrem terrible memory thalidomide trembling voice Velcade Warfarin white cells wind