{"id":1275,"date":"2011-09-12T11:11:06","date_gmt":"2011-09-12T11:11:06","guid":{"rendered":"https:\/\/scottysblog.com\/3-year-anniversary\/"},"modified":"2011-09-12T11:11:06","modified_gmt":"2011-09-12T11:11:06","slug":"3-year-anniversary","status":"publish","type":"post","link":"https:\/\/scottysblog.com\/home\/3-year-anniversary\/","title":{"rendered":"3 year Anniversary"},"content":{"rendered":"<p>Yes, it&#39;s a weird happy aniversary to me &#8211; three years today since I was diagnosed with the joys of MM. Still remember incredibly clearly, walking from one Parkside building to the other for some random test that I still thought was to do with my dodgy ribs (underactive thyroid \/ some muscular issue that could easily be sorted, so I thought). And also that I offered to carry the Parkside internal form with me, rather than have a staff member walk over&#0160;with me &#8211; no need for that I thought, they should spend their time on someone who really needs it. Ho ho-dee ho.<\/p>\n<p>Which did then lead to the great moment of me of course reading the A4 sheet of referral paper in triplicate, and spotting the mysterious words &#39;New Myeloma&#39; in the left hand column.<\/p>\n<p>&#39;What&#39;s this Myeloma thingy I thought? Sounds like Melanoma, but I&#39;m sure my ribs aren&#39;t suffering from excess sunbathing&#39;. &#39;Must be something to do with glands. Or ribs that need extra calcium to beef them back up again&#39;. What an interesting new word, I must find out what it is so I can bore&#0160;people&#0160;<\/p>\n<p>So I asked the poor sod in the X-ray department whose face was obviously a picture of &#39;oh god, no-one&#39;s told her \/ she shouldn&#39;t have seen the form \/ what the fuck am I going to say \/ how do I tell her she&#39;s just fallen into the &#39;monumentally screwed&#39; category \/ which idiot sent her here without a hand-holder \/ with any luck she&#39;ll die before she comes back here and I ever have to look her in the face again&#39; &#8211; amazing how expressive a face can be all in about 5 seconds!<\/p>\n<p>But &#8211; it&#39;s a good thing obviously, that I&#39;m still here. Making mistakes, trying to do things right, making the most of time, pissing people off sometimes when I don&#39;t mean to, knowing that some things I do &#8211; like for Mum &#8211; are bang on the right thing to do&#8230;. all the usual meanderings of life and trying to find your pathway through it.<\/p>\n<p>And given that the &#39;life expectancy of 2-5 years post-diagnosis&#39; which I went home and read starkly on the Internet that night is still deeply burned on my retinas, here&#39;s to 3 years. 3 years in which I&#39;ve had some bollock-brilliant times. Many cracking laughs. Some cool new experiences. Married my lovely man. Grown to adore my small furry feline black shadow. Got a new niece. And made the most of every day. Even those days when you go to the supermarket, empty the litter tray, order some&#0160;gubbins online, sort the bins out, look at kitchen tiles and buy some practical M&amp;S boots for your Mum&#39;s birthday- all days have to be good days, even if it&#39;s just a small thing that you think and smile about as you lie in bed that night.<\/p>\n<p>Thank god for the three years. It&#39;s more than I thought I&#39;d get. Here&#39;s to keepin &#39;em coming, Sx<\/p>\n<p>&#0160;<\/p>\n<p>&#0160;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Yes, it&#39;s a weird happy aniversary to me &#8211; three years today since I was diagnosed with the joys of MM. 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