https://forum.myeloma.org.uk/members/anne/activity/ Activity feed for cohenanne. Sun, 26 Apr 2026 17:30:30 +0100 https://buddypress.org/?v=2.9.4 en-GB 30 hourly 2 df667c2ee5ccd4ee2c3b7ad0fcddc88e http://www.myeloma.org.uk/forums/topic/22nd-of-november#post-96493 Sun, 03 Apr 2011 13:49:52 +0100 Re melphalan – i have read about people having this before SCT but is there anybody, who like my husband, is having it as a last resort treatment (we have been told he will never be able to have SCT as he never got a remission from CTD, velcade or revlimid – and there are no healthy stem cells to harvest. The consultant said the huge dose of…[Read more]

]]> 880b80e1232d8eef4498987945211312 http://www.myeloma.org.uk/forums/topic/side-effects/page/2/#post-103678 Sun, 03 Apr 2011 13:41:42 +0100 Thank you Keith and Min for your replies, its always good to know you're not alone, anne

]]> 27aa3999343edef4ab8c42a776fbc05e http://www.myeloma.org.uk/forums/topic/side-effects/page/2/#post-103676 Thu, 31 Mar 2011 22:25:08 +0100 Hi my name is anne, my husband was diagnosed last july. Since then he has been on CDT and velcade, both of which worked initially then failed. He was given revlimid, which gave him a bad rash which he had to stop. We were devastated that all these had not given remission. He has now been given an infusion of melthalon (slegehammer approach), but…[Read more]

]]>