Myeloma Forum | aurora | Activity https://forum.myeloma.org.uk/members/aurora/activity/ Activity feed for aurora. Sat, 11 Apr 2026 23:27:57 +0100 https://buddypress.org/?v=2.9.4 en-GB 30 hourly 2 2ff1ca6e1ef2cb72b06208fa54deb541 aurora replied to the topic hearing loss in the forum Side-effects https://www.myeloma.org.uk/forums/topic/hearing-loss/#post-132342 Sat, 18 Mar 2017 06:41:02 +0000 I developed tinnitus when Thaladomide dose was increased. It stopped when I’d completed 4 cycles. Didn’t have any problems immediately post SCT but it’s come back again in the last 2-3 weeks. As I’m not on any treatment at the moment I am slightly confused with what’s caused it.

I also developed  a numb lip during VDT treatment, but this also…[Read more]

]]> 11f487ae4fcc57df566fcd96b1b57bdb aurora posted a new activity comment https://forum.myeloma.org.uk/activity/p/43512/#acomment-45745 Thu, 09 Jun 2016 01:41:06 +0100 Hi Yorkyou
Read your post. I’d just drop a line to see how you’re doing.. hope the pain is getting better. When you find something that takes the pain away it’s a fantastic feeling. Take.care

In reply to - yorky became a registered member ]]> 4038ac1184d3f3b5fadb1a29cdcdef5a aurora replied to the topic New kid on the block in the forum Newcomers https://www.myeloma.org.uk/forums/topic/new-kid-on-the-block-2/#post-128398 Thu, 09 Jun 2016 01:31:12 +0100 Thanks Kempy for getting back. Chat rooms new to me as well.

MM wasnt on my game plan when I retired in April! Have had radiotherapy to plasmacytoma on back which finished today! Have spent the last 5 weeks in hospital on bed rest as tumour close to spine. Finally going home in spinal brace Saturday.  It was all such a shock at the time. Life…[Read more]

]]> 62b52882489576e135a3035344203c94 aurora started the topic New kid on the block in the forum Newcomers https://www.myeloma.org.uk/forums/topic/new-kid-on-the-block-2/ Tue, 24 May 2016 06:55:48 +0100 I was told 5 days ago that I had MM. innitially thought it was plasmacytoma but have low level active cells in bone marrow. Thought I would have a bit of time before the change to MM.  It seems so much to take in. I hate this loss of control and choice over what is happening to me.

 

]]> cebea5972f822b9f8505fabbd311ce12 aurora became a registered member https://forum.myeloma.org.uk/activity/p/45557/ Tue, 24 May 2016 06:22:54 +0100 1