Pollyanna Penguin’s RA Blog
This is a blog about me, my recently diagnosed rheumatoid arthritis and my struggles to stay positive about it!About Pollyanna Penguin
As already stated on the front page I’m not called Pollyanna and I’m not a penguin. My husband and some friends call Penguin though, and the Pollyanna part relates to my ongoing attempts to play ‘the glad game’ with regard to RA. Am I glad I’ve got it? Don’t be silly. But there are still plenty of positives to talk about … and when I’m having a negative moment I can come back to my blog and remind myself of them!
I’m forty-one, I’m female and if you’re a doctor and know the three f’s that relate to gall bladder problems, I’m the other f too, a bit. I don’t have gall bladder problems though … I do have rheumatoid arthritis (henceforth referred to as RA because I can’t spell it). I was officially diagnosed in February 2008 but suspected it since a ‘rheumatoid factor’ test (RF) came back positive in December of 2007, after I’d been suffering odd aches and pains in my hands, wrists and especially elbows for about a month. As I do a job involving a lot of typing I jumped to the carpel tunnel syndrome conclusion, but the doc said the symptoms weren’t right. She said while it was very unlikely, it was worth being tested for RA. To both our surprises the RF test came back slightly positive – I say slightly advisedly. My consultant tells me that people suffering from severe RA can have an RF figure in its thousands. Normal is zero to twenty – but most people are closer to zero than twenty. Mine was twenty-two. My immediate reaction was that surely that doesn’t really count – I was wrong!
I’m ridiculously happily married with a bunch of cats and no kids (entirely by choice on both our parts, and I suspect I could say all our parts and include the cats). I live in Norfolk, UK and I run a small business.
5 Comments »
Hello! I just turned 40 and was just dignosed with RA too. We are trying minocyclene therapy first becasue I am too chicken to do methotrexate off the bat. And I just can’t imagine not drinking! My rheumy said if insurance would agree to it she would put everyone with sereo positive RA on one of the biologics from the get go. I am still in the scared stage and figuring out what this all means to my life. I am so happy to find something that isn’t doom and gloom. I have a high RA factor but so far my inflammation numbers are very low so I am kinda a mixed bag. I’m in Denver in the US.
I have rheumatoid arthritis too. I was diagnosed at the age iof 24, 16 years ago. Each day is a challenge and yet I am grateful for any mobility I have.
I enjoyed reading through your blog and hope you will join us for Invisible Illness Week Sept 14-20. We are in need of guest bloggers and then will also have a 5-day virtual conference w/ 20 speakers. I also just began a new social network called Illness Twitters at htp://www.illnesstwitters.ning.com . Thank you for all you do to help bring more awareness to chroic illness and all that it entails.
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