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 »

  Alexandra Snyder wrote @

My name is Alexandra Snyder; I am the Content Editor at HealthCare.com. I’ve been reading your blog, Pollyanna Penguin’s RA Blog, and was really impressed by the content. I would like to invite you to syndicate your blog with our site.

We have a growing community of bloggers, health care seekers and care providers, and are one of the top online health communities in the U.S. We currently receive millions of visitors each month! By syndicating your blog to our site you will expose your work to the millions of users in our network and each post is featured on our home site. This is a great way to increase traffic for your existing blog/site and gain notoriety. Best of all, it’s simple, no need to write a separate blog or leave your current platform.

To feed/import your blog, you will first need to create a new blog account with us. This is done by clicking “create my blog” from this link: http://blogs.healthcare.com . A request will be sent to me and it will be put in queue for approval. Once approved, an activation email will be sent to you, simply click the link and follow the import instructions found (here). If you run into any problems, please refer to our FAQ page or email me.

Have a great day!

  Melissa wrote @

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.

  pollyannapenguin wrote @

Hi Melissa, Sorry you’ve got this horrible thing, but I really hope the minocyclene does the trick for you. I think everyone with RA is a mixed bag in one way or another, in the sense that no two people actually seem to have the same symptoms! As to mine, they keep changing day by day – baffles the consultant. ;o) It’s so hard to figure out what it means to your life – but hopefully it’ll been a short blip while your rheumy gets it sorted out and then you’ll be OK!

Really interesting about the insurance – there was I thinking if we had the American health system over here I’d be able to get biologics straight away – HA! They’re all as bad as each other!! (Oops – that wasn’t very positive was it? Sorry!) ;o) (It’s too early in the morning here for much positivity!)

  Lisa wrote @

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.

  myfibro wrote @

Hello there!!My name is Joanna and I have Fibromyalgia..Its not RA but some symptoms are very similar,pain for example loool
Im commenting because I love people who try to stay positive!Thats what i struggle for..My worst fear is loosing my positive attitude!!!I hope we can keep in touch,I also love UK!


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