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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 me Penguin though, and the Pollyanna part relates to my ongoing attempts to play 'the glad game' with regard to RA. (Blogging community friends now mostly call me Polly!) 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-nine 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 something like 25. My immediate reaction was that surely that doesn't really count – I was wrong!
I'm ridiculously happily married with a cute black cat and no kids (entirely by choice on both our parts, and I suspect I could say all our parts and include the cat). I live in Norfolk, UK and I run a small business.
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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!
Comment by Alexandra Snyder— July 3, 2008 #
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.
Comment by Melissa— June 18, 2009 #
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.
Comment by Lisa— July 10, 2009 #
Dear Pollyannapenguin,
I am working with NRAS the National Rheumatoid Arthritis Society to organise and promote a series of 10 UK based events helping those with RA to keep working. We are looking to publicise these events online. I found your blog via Google, and thought you may like to help – as you have a group of regular followers all of whom have RA, and I think would find this really useful.
The workshops will be held throughout 2010 in cities all across the UK. They're open to anyone with RA and they're free. Each workshop will help attendees get information about talking to your employer and colleagues about RA
o share practical tips based on real-life experience
o talk to experts, from employment lawyers to occupational therapists
o find out more about what disability law means for you
o find out more about handling your RA treatment and work commitments
The workshops will be held in: London 24th February; Bristol 10th March; Cardiff 11th March; Manchester 18th May; Birmingham 19th May; Nottingham 20th May; Glasgow 22nd June; Londonderry 23rd June; Portsmouth 7th July; Reading 28th September.
Registration is happening now and make sure we can fit everyone in a room. To do so, or to find out more, we can be rung us on 0845 458 3969 or visited http://www.nras.org.uk to register online.
I have pdfs of the flyer for all the events, and the poster for London where the first one is on Wednesday night.
Can you help? We are nearing the first one, have promoted this in hospitals, through NRAS but really want to pack the room with people who can benefit from this. People like your readers.
Best regards,
Comment by Tim Scorer— February 18, 2010 #
Hi. I was diagnosed with RA in 2007. I had a flare in my left hand at the joint near my wrist above the thumb. I was in excrutiating pain and could not use my left hand. I went to my GP that day who in turn referred me to to a rheumatologist. I was diagnosed with severe RA. I began with 5 methotrexate pills (taken all at once , once a week). That didn't work and I was increased to 7, then to 8. Still no results. The doctor then added Remicade IVs to the recipe – every six weeks. My liver functions began to elevate and by the 4th week after receiving the IV I was in flare ups to the point I could barely walk, never mind sleep. I begged God to take me. My Rheumatologist then took me off the Remicade and started me on Rituxan (still taking methotrexate. This drug works! Thank God. I felt that Rituxan saved my life. I still take the 8 methotrexate pills every Wednesday, but I only go in every six months for my Rituxan IV. I have a friend that has RA and she will not take these meds because she is afraid of the side effects. I've had no side effects from my current treatment and will do anything to fight this disease as I do not want to become a cripple even if there are mild side effects. If anyone out there has any doubts about Rituxan, please, please reconsider, because it really has helped me considerably. I feel strong again, I feel very little or no pain and I have a new outlook on life. I have a life now. I just painted my living room and bedroom and it didn't bother me in the least.
Comment by Carmen— March 16, 2010 #
Hi…loved ur blog…ist dx was RA changed about 5 yrs ago to Psoratic arthritis. I have had it for about 40 years. Came out with it about 20 y/o and now I'm almost 60. The differance, I was told, is where the autoimune part comes from. Something I found out and I'm not sure if you know this or not…but along with the inflamation of RA….comes the same imflamation in the blood vessleswhich is heart disease. The good news is that I have been on EMBREL for about 9 years and I am pleased to report that I am doing well. Hope you will feel better…bye
Comment by Marikay— April 13, 2010 #
THANKS for such a positive Blog. I read a few of the different blogs out there and it seemed like so many were so negative. I am 57, was diagnosed with RA at 19, have had over 40 surgeries (multiple replacements), walk about 2 miles a day now (could not always), 2 sons, 2 granddaughters, awesome husband, supportive family, and have managed to keep on going. The most important thing I learned over the many years living with "Arther" is a positive attitude is 1/2 the battle with this disease. The second is acceptance. I have had many ups and downs through the years but seeing good in everything has also helped me get to where I am.
I live in TX and it is heartwarming to read about someone else who has found the magical secret that staying positive is a powerful medicine in its self.
God Bless You!
Comment by Candy— April 20, 2010 #
Hello Pollyanna, my husband is 34 and has had aggressive RA for a year now, which has turned our lives upside down. We have been looking for local support sites or just something that a young man with RA can relate to but there seems to be very little out there. I know that statistically it's more likely to be women who develop RA and there is quite a bit out there on the web but it's never something he can relate to – the loss of his position as provider for our family and the loneliness of spending day after day at home whilst putting a brave face on to me and the kids. Do you know of anything that sounds like it would be suitable? I'm encouraging him to start a blog, I think it's a great idea and I will be following yours with interest.
Take care and stay positive! Emma xx
Comment by emmaalice— November 24, 2010 #
hi there… i've never been on a blog,,ever, but was diagnosed with RA about a year ago… quite by accident i went to to the doc, for an horrific pain in my hand, which jumped to the other hand (what's up with that?)… had some bloodwork and was put on prednisone… got better.. than goodness… (could not believe i could not even grip the t-paper??? yikes… anywhoo… i was sent to a Rhumetologist (please bear with the spelling..)just to "rule out RA"… and guess what… can't rulle it out.. so, cutting to the chase… i've got a wonderful doc… he finally convinced me to "do the meds"… folic acid,hydrocloriquin,methotrexate… weekly… have not had another flair up , very lucky ,, stiff, but heck i'm getting old so most of it is expected… but here's my question…. i don't really know what to expect… i am "tired" a lot more", but i'm gonna be 64, so don't expect to move like 40… and seem to be depressed a bit,,, i'm a bit worried about "side effects" of my meds… am i being stupid and should just be greatful, or can someone tell me what to expect ,,, are flare-ups inevitable??? I'm a pretty tough chick, so not afraid of pain, just want to know what to look for or expect…
So, i'll be reading diligently and hope i can become a good member of my 1st. BLOG!!!! 🙂 bj
Comment by barbara johnson/bj— March 8, 2011 #
Hi BJ, and welcome to the exclusive club of RA sufferers! Well first I suppose I should say I'm no medic, so these are just my thoughts and opinions, but OF COURSE you're worried and a bit depressed. Who in their right mind wouldn't be? 🙂 However, it's great news that the mesd are working for you! You're on the same bunch as I am, by the sounds of it, and most of the time they're working for me too.
I always bang on about this, but to my mind the most important thing to remember when looking at blogs or reading leaflets or talking to the medics, and especially talking to friends and relatives, about RA, is that EVERYBODY IS DIFFERENT! Just because you read somewhere that someone has flares every few weeks, doesn't mean you will. Just because some people suffer side effects to methotrexate doesn't mean you will etc.
Flares are not inevitable – they might be if you weren't on the meds, but if you get the right dosage then you could go without flares for years or even for ever!
Fatigue certainly does seem to be a big part of RA and, in my experience at least, not something the medics take as seriously as they might … perhaps because it's harder to measure than inflammation and swelling! You really need to learn to pace yourself. (I'm rubbish at practising what I preach here, but it's so important!)
You might want to ask your doc for a referral to an occupational therapist (might be called something else where you are, as that's the UK term) A good lecture from mine now and then keeps me on the right track! 🙂
As to side effects, here's the thing … most people don't have ANY! Of course you hear about them – they can be grim and that makes them newsworthy! But if most people had terrible side effects and couldn't continue on MTX then the FDA would ban it. It's still the 'gold standard' although biologics, the relatively new drugs, are probably going to take over soon. I'd say so long as it works for you, keep taking it, don't worry, enjoy life … I'm sure that should be easy for a tough chick! plenty of time to get depressed if it stops working or causes side effects. 😉
Comment by Polly— March 9, 2011 #
:).. thank you so much Polly… i'm gonna love this place i just know it…i was thinking "how lucky" i am, so it's good to know it's also possible to stay that way!!!! LOL
first… i noticed you are reading SCARLET… LOVE that book!!! and then i realize you are in the UK.. I'm a BBC masterpiece "junkkie" and love all things past and especially british!!!
I live in a retirement comm. in MA (USA) and i'm so lucky that DH moved us here.. check it out if you want…. http://www.oakpointhomes.com!
I can swim all year, and that's a huge plus.. i was going great guns last year, but then hit a bump, when i had emergency surgery on my "gut" (for lack of a better term)… but i'm all fixed and life is good… today, a bit sad… my DD has lost her FIL, after a long fight with diabetes.. but he is a piece…
so.. i'm a "funky retired broad" 63.. and can't believe that… with tons of support and friends.. i hope i can bring some smiles to this blog, and will be very greatful for the info i can get here… hugs bj/barbara
Comment by barbara johnson/bj— March 9, 2011 #
Hi "Polly"
As you know, May is national Arthritis Awareness Month. I invite you and your blog community to participate in an important national survey being conducted this month by Flexcin International, available by clicking on this link https://www.surveymonkey.com/s/flexcin. A proceeds sponsor of the Arthritis Foundation, Flexcin will reveal results of the survey for Arthritis Awareness Month in May.
The survey is open to anyone suffering from any form of arthritis, Osteoarthritis, Psoriatic arthritis, RA, gout, joint pain, lupus or other joint-related pain, illness or disability. The purpose is to get a better picture of how aware other people are when any number of family members, friends or co-workers have arthritis or a joint pain-related disease. The twelve-question survey will help paint a picture between men and women coping with arthritis, and the level of support they receive on any given day. Please feel free to blog about the survey. Let me know if you'd like a copy of the results in early May.
Comment by John Sternal— April 12, 2011 #
Hi "Polly"!
We are interns at the Arthritis Foundation, Northern California Chapter and we are very impressed by the content of your blog. We are doing a summer project in order to increase Arthritis awareness and advocacy. If you are willing to answer a few questions for us regarding your experience with Arthritis, please email us at email@example.com. Thanks so much for your time!
Comment by Iliyana Gesheva— June 20, 2011 #
Thanks for the bright smile. I too have RA and can't spell it either. Thank god for initials. I also have MS. I am waiting for the next initial disease to hit me. Makes life easier, but you would not believe the people who don't know what RA is nor do they know what MS is. Hopefully they will remain blissfully unawakened. Thanks for the blog. I truly like it. I am 66 so I am much your senior, but only found out I had RA this year (2011) and MS in (2004). Oddly enough I think my meds for RA are also helping my MS. But the MS shots are sooooo expensive. Once again thank you.
Comment by Carole Beasley— December 12, 2011 #
[…] Penguin's RA Blog About: Sie ist glücklich verheiratet, lebt mit ihrem Mann und ihren Katzen in Norfolk, UK und leitet ein […]
Pingback by Will I never learn? by Polyanna Penguin « Mein Rheumatoid-Arthritis-Code— March 19, 2012 #
I work for JMGlass, a marketing company offering a variety of products benefitting those suffering from arthritis. I would love to partner with you to advertise our products on your blog, and possibly send you a complimentary giveaway. Please provide me with a contact email address.
I look forward to hearing from you.
Ramona Joseph
Comment by Ramona Joseph— March 20, 2012 #
Hi Pollyanna
It seems good information about a rare form of arthritis called palindromic rheumatism is hard to come by, but I'm hoping some of your readers and bloggers can help put that right. I'm doing some work for the charity Arthritis Research UK, which wants to develop information materials to help people with palindromic rheumatism manage their condition. As a first step, we want to talk to people who have been diagnosed with the condition. It's characterised by unpredictable flares of pain and swelling in joints, which return to normal between attacks, and can have life-changing implications. As you rightly say, everyone is different, and with so little research into palindromic rheumatism, we want to hear at first hand what it's like to live with it, how it affects people and what their experiences of getting a diagnosis were. We'd like to invite anyone among your contributors and readers who has palindromic rheumatism to take part in a survey between April and July 2013. All they have to do is complete a short online questionnaire at http://www.arthritisresearchuk.org/palindromic. If they agree, we'll then contact some by phone to hear their palindromic rheumatism story in more depth.
Meanwhile, thanks for the very positive blog about RA.
Comment by Anonymous— April 9, 2013 #
Hey Pollyanna,
I wanted to get in touch because I think you might be interested in an interactive web page we are currently working on to raise awareness for RA.
Because it is Arthritis Care Awareness Week very soon (13-19 May), I believe this would go really well on your blog, and be of great interest to your readers.
Our infographic will be visible on a web page which we will share with you once completed.
We have a teaser snippet of the infographic to give you a first viewing so let us know if you want us to send that over! You are more than welcome to embed this on your website as well. We hope you help us in raising awareness for RA and spread the word!
Let me know if you would like any more information. I look forward to hearing from you.
Kind regards,
Comment by Lucy— May 1, 2013 #
Hi Pollyanna
I stumbled upon your blog and would appreciate any help in getting in touch with RA sufferers.
I work for a small UK company that manufactures a cooling bandage. We are receiving increasing feedback from RA suffers who are using our products to reduce inflammation and pain.
I would like to give away free product in return for feedback and have attached a link to a testimonial we received from the son of a lady who uses Physicool to reduce her pain and inflammation: http://www.physicool.co.uk/injury-guides/arthritis/.
Please do get in touch. As a first step I am happy sending a bandage to you to use and trial.
kind regards,
Comment by Physicool (@physicool1)— July 30, 2013 #
Hi Polly, it's Ian here from Physicool. I replied to your email but have heard nothing back. Did you receive my message? Please get in touch (firstname.lastname@example.com).
Many thanks,
Comment by Physicool (@physicool1)— September 23, 2013 #
I hope this finds you well. I represent Healthline Networks, and we were wondering if you could include Healthline's Rheumatoid Arthritis Center (http://www.healthline.com/health/rheumatoid-arthritis) as a resource on your page: https://pollyannapenguin.wordpress.com/
Healthline provides a very comprehensive overview of Rheumatoid Arthritis as a critical starting point for individuals and/or their loved ones.
Why you should include Healthline as a resource:
-Video overview of RA by Dr. Paul Auerbach of Stanford Medicine
-A free interactive educational tool on RA: http://www.healthline.com/rheumatoid-arthritis/anatomy-animations#1/what-is-rheumatoid-arthritis?
-Breaking news (ex. http://www.healthline.com/health-news/arthritis-gum-disease-bacteria-worsens-rheumatoid-arthritis-091713) and in-depth, doctor-reviewed content
For more information about our rigorous editorial process, to view our board of directors and more visit the Healthline about page: http://www.healthline.com/health/about-healthline.
Please let me know if you are open to adding Healthline's RA center as a resource. Thank you in advance for your consideration, and I look forward to hearing back from you.
Comment by Maggie Danhakl— October 26, 2013 #
Hi, I came across your blog, and thought you might be interested (or know of someone who is interested) in participating in a research study about managing daily living skills while living with RA. It has been developed by Occupational Therapists in Canada (Edmonton, Alberta to be exact – there are a large number of RA sufferers in our Northern environment!). Details can be found here: http://screencast.com/t/w5BSzNw0 Feel free to connect with me on twitter @RAfighters if you'd like more detail. Liz
Comment by Liz— November 20, 2013 #
Thank you for all the work that you and your blog do for Rheumatoid patients. I'm a chronically ill epatient working on HealClick, a website matching patients with similar conditions so they can share relevant treatments and experiences. I'd love to talk with you about the possibility of working together. Feel free to email me directly at firstname.lastname@example.com.
Comment by Rachael— January 2, 2014 #
Dear "Polly": (sorry!)
My name is Kathleen Engel and I am an editor at Health Monitor Network in Montvale, NJ. My company publishes guides on various health conditions that are distributed free to patients through doctors' offices. (You can see our site at healthmonitor.com.)
Right now I am working on an article for the next issue of our Guide to RA. (If you'll send me an email address, I'd be happy to send you a PDF of an older issue so you can see what the guide looks like.) The article is a roundup of tips from a number of contributors that I hope will be helpful for our readers with RA (who will pick up this guide in their rheumatologist's office). The idea is roughly "Tips to help you cope with your RA around the clock."
Are you able to contribute a tip or two, Polly? I would love to run your quote along with your photo. I am looking for self-care tips that you do that I can tag to some point of the day: Upon waking up, breakfast, mid-morning, Noon/lunch, afternoon, dinner, evening, bedtime, while sleeping.
Tips could be anything interesting that you do that helps with your RA, from meal prep tips, to a smoothie you always make at 10 AM, to meditation, exercise, a special pillow that helps you sleep, a stretching routine, warm bath with Dead Sea salts or whatever helps YOU. Also, tips can deal with anything that is a part of RA, not just the pain, but fatigue and brain fog, too. (I'd just ask you to tell me why you're doing it. So, for example, the smoothie—maybe you've found it quells your mid-morning cravings, which is helpful for keeping your weight down.)
The only caution: I can't include anything about medication.
Thanks, Polly. I look forward to hearing from you and do hope to include your comments. Once the guide is printed, I'm happy to send you a PDF and, if you'll send me your mailing address, hard copies. If we put it on our web site, I can send you a link you can put on your blog, if you like.
Any questions, please let me know!
Kathleen Engel
Editor, Health Monitor Network
PS – Great blog! And sorry to call you Polly!
Comment by Kathleen Engel— June 3, 2014 #
I've just been diagnosed with RA, I'm 36 (and a half!). So far I'm just on prednisolone and I feel like a million dollars but I'm afraid of what's to come because I don't know what to expect. I've joined the gym, I'm working out regularly, I'm eating really healthy, I'm staying really active and positive but I'm reading about all these horrible side effects of the Prednisolone and I don't know what to do to help avoid them, or if that's even possible. I know over the course of the next couple of weeks my dosage will reduce but how much of this prednisolone must you be on to put up all that weight? And I'm feeling really positive and focussed now but what if I start to feel depressed and I lose the motivation? I just don't know what to expect and no one seems to be able to tell me.
Comment by Trish— March 9, 2015 #
Tanya apart from your positive attitude what else did you do to improve your arthritis?
Comment by Mike O'Brien (@psori_arthritis)— June 1, 2015 #
Hello, Great blog! Do you have an email address I could contact you on? I work at an Arthritis Charity and we're looking for bloggers just like you to be apart of it! Thanks, Emily
Comment by Emily— September 9, 2015 #
Hi (not actually called) Polyanna!. 🙂 So great to see people blogging and helping each other out in this worldwide autoimmunity epidemic! Please bear with me if you don't know me… I am not selling anything or taking advantage in any way. I suffered horribly with psoriatic arthritis and other autoimmune issues, but rejected medication and decided to go my own way with it, studying and experimenting for years until I succeeded in reversing it. This book is my story from diagnosis to success with all the crazy wrong turns and magical discoveries that happened in between (with a foreword by well-known neurosurgeon and biohacker Dr. Jack Kruse). I'd like to just let you know that it is FREE on Amazon Kindle for the next three days from the 26th, so if you'd like a copy, go and grab one. I really hope that my story inspires, and if you'd like to leave an honest review, I'd be very grateful.
Link below to Amazon US, but it is available in all territories.
Kind regards,
Comment by Phil— July 26, 2016 #
Love that you are sharing the story of your experience with Rheumatoid Arthritis. And I love your outlook and sense of humor, I think it is too easy to overlook how big a role overall mentality plays a part in any bodily condition.
Have you had any experience with taking Turmeric to try and reduce inflammation from RA? Our company http://www.turmericvitality.co.uk/ specializes in turmeric for this purpose.
Regards, Josh – Turmeric Vitality
Comment by Josh— September 27, 2018 #
Hi 'Pollyannapenguin'! My name is Rhona and I'm a 3rd year Product design student at the Glasgow school of art doing research on sufferers of forms of Arthritis for my 3rd year project. I would love to get in contact with you to ask you some questions for my research, would this be at all possible?
Please let me know ASAP at my email address!
Best, Rhona
Comment by Rhona Brown— February 13, 2019 #
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For me, Windows 8 is a tale of two cities: There's an abundance of cool new features that I love, balanced out by an abundance of design changes that I absolutely hate. I accept all of that. Major changes bring major transitions. But as a card-carrying, freedom-loving geek, there's one thing about Windows 8 I simply cannot accept, a "feature" that seems shiny and new and nice, but hides dark and dangerous possibilities that could devastate computing as we know it and leave us all shackled in Modern-styled chains. Even worse, that ticking time bomb beats as the heart of the new Live Tile interface, a malign tumor threatening to eventually rot the PC's open core.
The Windows Store. The harbinger. Microsoft's closed-off answer to Apple's vaunted walled garden.
Skin-deep beauty
Don't get me wrong; I have no problem with the usability of the Windows Store itself. No matter what type of device you're using, the Windows Store is slick, polished and easy to browse, especially with the help of Windows 8's new "type to search" feature. Its interface sits heads and shoulders above the Apple and Android alternatives.
No, my issue lies with the philosophical underpinnings beneath the attractive veneer.
The only way to get Windows 8 apps is through the Windows Store, some enterprise and developer exceptions aside. And the only way to get into the Windows Store is to go through Microsoft; developers need to pay for a license, submit their apps for approval from on high, and pray to get in.
The new walled garden approach holds a number of advantages for casual and neophyte computer users. Since Microsoft approves the content, Windows 8 apps are sure to be functional at a base level and free of malware. That security comes at the price of freedom, however.
The only way to get Windows 8 apps is to go through the Windows Store, and Microsoft's app guidelines contain a laundry list of rules that tell developers what types of apps will be approved. Microsoft, like Apple, plans to actively screen the editorial content of apps to avoid offending delicate sensibilities.
A poisoned Apple
Just search Google for "Apple censors apps" and similar phrases to get a feel for what happens when an entire ecosystem's content flows through a single source that considers itself a moral authority. Apple has censored iOS apps from satirical Pulitzer Prize winners, apps from religious groups, apps with political motivations, Google Voice, apps with Dropbox hooks, any app that overlaps the functionality provided by the core iOS experience, and a whole lot more.
Microsoft allows apps with competing functionality into the Windows Store, but it controls editorial content with an iron fist. Here are the content guidelines for Windows 8 apps:
- Your app must not contain adult content
- Your app must not contain content that advocates discrimination, hatred, or violence based on membership in a particular racial, ethnic, national, linguistic, religious, or other social group, or based on a person's gender, age, or sexual orientation
- Your app must not contain content or functionality that encourages, facilitates or glamorizes illegal activity
- Your app must not contain or display content that a reasonable person would consider to be obscene
- Your app must not contain content that is defamatory, libelous or slanderous, or threatening
- Your app must not contain content that encourages, facilitates or glamorizes excessive or irresponsible use of alcohol or tobacco products, drugs or weapons
- Your app must not contain content that encourages, facilitates or glamorizes extreme or gratuitous violence, human rights violations, or the creation or use of weapons against a person or animal in the real world
- Your app must not contain excessive or gratuitous profanity
In other words, Windows 8 apps are so many bricks in the wall(ed garden), thought-controlled and scrubbed squeaky clean to Microsoft's new Leave It To Beaver-esque standards.
A Dark Age ahead
Microsoft's a private company, of course, and it can impose whichever arbitrary and heavy-handed rules it wants. However, a large part of Windows' past success lied in the relatively open nature of the operating system. (Cool it, Linux lovers.) If you wanted to create a new piece of software, you just whipped it up and slapped it on the Internet — no costly developer license, jumping through censorship hoops, or 30 percent cuts of revenue to Microsoft required. There is a reason that Windows shined while Mac stuttered and iOS users strived to jailbreak their locked-down phones.
Microsoft is gutting its legacy, sacrificing its past on the altar of the tablet gods.
I'm not the only one who thinks so. When Microsoft asked Minecraft's developer Notch to certify the game for Windows 8, he told them to "Stop trying to ruin the PC as an open platform." He didn't stop there. "I'd rather have Minecraft not run on Win 8 at all than to play along," he tweeted.
Minecraft can, of course, still run on Windows 8 thanks to the Desktop mode, which plays classic-style Windows programs just fine. Windows RT tablets don't have the same privilege; they're stuck running those squeaky-clean, Microsoft-approved Windows 8 apps alone.
The focus is firmly on the new apps and interface, however. Windows 8 takes great pains to shove the Desktop and its legacy programs into a dusty, dark corner. The entire Modern-style Start screen revolves around glittery, transforming Live Tiles generated by Windows 8 apps, while the entire Desktop functions as a single app in Windows 8's Switcher, no matter how many classic-style programs you have open. Microsoft doesn't even allow users to boot to the Desktop directly from start up — you must go through the Modern Start screen.
Unless even users complain and Windows 8 fails miserably, I expect the non-enterprise versions of Windows 9 to be the final bricks in the walled garden, ditching the Desktop completely and leaving users with no choice but to look at the world through glasses colored whichever hue Microsoft decides to approve.
A happy medium
It doesn't have to be like this. The newbie-friendly benefits provided by a walled garden are huge, and I can understand Microsoft wanting to hand-approve apps that sink deep hooks into Windows 8's core.
I'm a big boy, though, and I want choice. Grand Theft Auto IV wouldn't have been anywhere near as fun if Packie didn't swear like a sailor and Niko laid down his automatic weapons and alcoholic beverages. Fortunately, there's already an example Microsoft can follow that would dispel all my negativity and doubt: Android and Apple's own OS X desktop operating system.
Both of those platforms restrict users to central, approved download sources out of the box, which provides casual users with the same level of security and ease-of-use currently offered by the Windows Store. More crucially, they also provide a way around that barrier for power users. Sideloading apps on Android is as simple as switching out a system setting, while disabling Gatekeeper on a Mac is just as straightforward.
Adding a sideloading option for everyone — not just devs and IT admins — would allow Microsoft to have its cake and eat it too. Casual users could stay safe and secure, while power users could bask in the open freedom and continue to use their computers as they see fit.
Sideloaded apps wouldn't be subject to Microsoft's 30-percent Windows Store fee, of course. That shouldn't make too much of a dent in company revenues; as I said, Android allows sideloading, and I don't hear Google complaining that hordes of users are snagging apps from third-party sources. However, allowing sideloading would let developers distribute Windows 8 apps that are too edgy, mature, political or religious for Microsoft's squeaky-clean enforced tastes, while maintaining the open tradition the operating system is known for.
Will Microsoft grant this boon after already tossing out the Start button, the desktop and the company's reluctance to make its own hardware, or will it continue down the ham-fisted (yet profitable) path blazed by the dictators at Apple? That remains to be seen. But if the company doesn't change its ways, the Windows Store will be the death — not the evolution — of computing as we know it.
Keep on keeping on with that Steam for Linux endeavor, Valve. You might just be sowing the seeds of rebirth that keeps hope alive after a computing apocalypse.
The views expressed here are solely those of the author and do not reflect the beliefs of Digital Trends.


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Fixed-rate mortgages are characterized by their interest rate (including compounding frequency, amount of loan, and term of the mortgage) and are known for their ease of comprehension among borrowers. Unlike adjustable-rate mortgages, fixed-rate mortgages are not tied to an index. Instead, the interest rate is set to an advertised rate, usually in increments of 1/4 or 1/8 percent.
Fixed-rate mortgages are usually more expensive than adjustable-rate mortgages. Long-term fixed-rate loans will tend to be at a higher interest rate than short-term loans because of increased risk. They are usually available as 30-year, 15-year, 10-year, 20-year or 25-year fixed rate.
An adjustable-rate mortgage (ARM) is a home loan in which the interest rate changes periodically based on a standard financial index. ARMs generally permit borrowers to lower their initial payments if they are willing to assume the risk of interest rate changes. They transfer part of the interest rate risk from the lender to the borrower, who benefits if the interest rate falls but loses if the interest rate increases. This creates the risk of financial hardship to the borrower. To limit this risk, most ARMs have caps on how much an interest rate may increase over the initial term and life of the loan.
An FHA Loan is a government mortgage loan partially insured by the Federal Housing Administration, which covers lenders in most losses if a borrower defaults. FHA loans have historically allowed buyers to borrow money for the purchase of a home that they would not otherwise be able to afford. Typically, a reduced down payment of 3.5 percent is required. FHA loans are assumable for owner-occupant borrowers.
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A rural housing loan is a government mortgage loan guaranteed by the U.S. Department of Agriculture (USDA), which allows 100 percent financing. The home must be located in a designated USDA area and the borrowers must have certain income limits to qualify.
Bond loans are government mortgage loans made through state-sponsored loan programs to lower the cost of homeownership for low-to-medium income borrowers, sometimes for targeted occupations or neighborhoods. This type of loan may include State Down Payment Assistance, which varies by amount and is offered subject to income limits.
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Now, I've read the comments about this comic on my previous thread, and there's been a huge debate over whether this comic constitutes good art or not. And I think people on both sides of the argument have made it clear that they will kill me if I do not agree with their side. So, knowing that by wading into this debate, I open myself up to certain death, I have to say that I do like it.
It's not a timeless classic, of course, and some people who seem more knowledgeable about computer art than I say it isn't even that difficult. No matter. I still like it, and not just because it's better by far than the usual standard. It may not be realistic to have the ocean be totally dark right next to the sun, but whatever. When I ask for better art in xkcd I don't mean photorealistic art, I just mean art that helps the comedy, which this does (to an extent). Here, look at the big version.
Leaving the quality of joke aside for now, the point is that one character is trying to use the sunset to distract another. If we just had a crappy black ink on white page version of this comic - which I would sketch out if I had more time but I am sure you can imagine it in your mind - it wouldn't be as effective. Seeing some that much more closely approximates a real sunset makes your mind start to think about times that you have looked at sunsets, it makes it easier to imagine a person staring at this while a man in a hat steals his car. In other words, (and i haven't expected to say this before) the art does help support the story of the comic.
Of course, the story is lame. The story is "look at the sun while I steal your car," with a car that happens to be popular to nerds these days thrown in. That's it! It makes for quite the contrast with the art, though not in a nice way. Besides, Mr. Hat is supposed to be diabolical, not so stupid that he tells the dude exactly what he is scheming. Look at it! He's actually saying "stare at the sun for a while as I drive away in your car." Come on! I'd be happier with the no dialog version, as linked to above. Maybe some weapon clearly visible in Mr. Hat's hand, or something.
In the end, it's a rare step towards art and words that compliment each other in xkcd. I'd be setting myself up for disappointment if I expect more of this, but at least he isn't denigrating an entire field of study or showing people carefully plotting pregnancies.
DAYS SINCE THE LAST XKCD BLOG UPDATE: 61 (two full months!)
DAYS THE XKCD "ANTHROPOLOGIZE" MESSAGE LASTED ON XKCD: 2 (it's not even up on the original comic anymore! sucks to be an anthro major who reads the comic later!)


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I have been doing lots of sewing, applique and embroidery for the past few days and I feel like it's finally paid off. I tried to keep it as simple and as fresh looking as possible with accents of feminine colour.
For those wondering I used a tiny £60 sewing machine from Argos which has been brilliant! I hand stitched the applique on to the bedding and then hand embroidered the 'cross stitch' with the brown for extra decoration and to bring it alive.
I knew I wanted a bird Incorporated in the design and here's what the little birdie looks like with it's pretty bow! :)
Here's the heart decoration I gave you a sneak peak of in a previous post...
It ties from the sides with cotton ribbon and I placed it on top of the bumper, I can move it around wherever I want in the future.
I also made an underskirt sheet to cover the bottom bit of the cot so I can use under the bed as storage but keep it looking clutter free.


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Industries, 2018 Cycle
This group makes independent expenditures from their hard money funds. They do not collect "outside spending" specific donations. Click to see their hard money donors.
Based on data released by the FEC on February 01, 2019.
Feel free to distribute or cite this material, but please credit the Center for Responsive Politics. For permission to reprint for commercial uses, such as textbooks, contact the Center: email@example.com


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Convey an air of sophistication with the beautiful Amerock Allison Collection. Choose from a range of exceptional cabinet knobs, cabinet pulls and appliance pulls that will really create a lasting impression on anyone who comes into your home. With almost one hundred years in the business, you can be sure Amerock is doing things right. Come in, and let the Amerock Allison Collection take care of you.
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About Mattias Fredriksson
Mattias Fredriksson loves to ski. He also loves to photograph his friends while skiing and has been doing so for 15 years. Mattias lives in a mountain town called Are and that's in Sweden. He travels the globe in search of great snow. He also shoots campaigns for some of the biggest companies in the ski industry.Website: http://www.mattiasfredriksson.com


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Wow Your Valentine
Your Valentine's Day table doesn't have to be overwhelmed with Xs and Os. Create a sense of simple, understated romance for your Valentine this year with these versatile table decor ideas.
Understated Romance
Incorporate versatile decor pieces like metallic-clad flatware and candlesticks. These items not only pair perfectly with everyday elements like white dinnerware, but the combination creates a beautiful palette that can be used on many occasions throughout the year.
via The Pretty Blog
Fearless Floral
If time simply doesn't allow, forgo the new decor and head straight for the florist. We promise, with a decadent centerpiece or delicate floral garland, your Valentine won't miss their annual bouquet of a dozen roses. Pair with a basic, complimentary table linen and your everyday dinnerware and voila!
Charm With Chocolate
Is your Valentine a chocoholic? Line the table with a thoughtfully curated sweet, like these handwritten chocolate glaze cupcakes. Or, keep it simple with an array of Valentines chocolates.
via Martha Stewart
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Rope Twisted Design Carved Resin Vintage Style Bangle Bracelet
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रोते हुए आओगे हँसते हुए जाओगे ।
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Renaud Evrard received a PARE grant for a proposal entitled "Differential clinical approach to exceptional experiences : from traumatic to growth processes in teenagers and adults."
Alexander Batthyany was granted for "Retroactive Priming: The Impact of the Need to Evaluate and Affective States."
David Luke received funding for "The effects of mescaline-containing cacti (San Pedro) on psi: A pilot study Ecuador."
Register with the Parapsychological Association website to participate in the discussion, or sign in if you already have an account.
The Parapsychological Association is an international professional organization of scientists and scholars engaged in the study of psi (or 'psychic') experiences, such as telepathy, clairvoyance, psychokinesis, psychic healing, and precognition. The primary objective of the PA is to achieve a scientific understanding of these experiences.
First established in 1957, the PA has been an affiliated organization of the American Association for the Advancement of Science (AAAS) since 1969. The PA is a non-profit, non-adjudicating organization that endorses no ideologies or beliefs other than the value of rigorous scientific and scholarly inquiry.


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Hello everyone. Today's post concludes my guest week and in order to get you used to carl again, I decided to be fashionably late with it. Actually, I just didn't know what to write. At the time of writing, I still don't. Let's just see what happens.
Ok, uhm. Well, I know something I can say about this. The art, as always, is extremely mediocre.
You don't even notice it, but more than half of the comic is text, and once you reduce it to the actual pictures, you get an absolutely meaningless scene. Comics are a visual medium. Xkcd is not.
Now let's try that the other way around. I will replace all of the art with two monochrome boxes:
Is it much worse than the original? The only thing the art clarifies is that the black box is quoting this from a book, other than that, it's the exact same thing. Now, I'm not saying that this xkcd is a fucking masterpiece, but it could and should be better. Let's mash it up, SMBC style. Sorta.
This is something Randall presumably found out one way or another and came up with this plan to scare a friend, and then decided to make it a comic. Why he didn't use mr. hat is beyond me, but whatever. The problem is just that it's not really that funny to begin with, mostly because the explanation needed is a bit long, but also because he's not exactly doing a good job at delivering it. Overall, the comic is pretty meh.
I don't even really know what to say about this one, and the forumites don't either, they're just talking about whether they had that dream. Some are saying GOOMHR which is bullshit because he didn't come up with the fact that these dreams are common. Fuck you, forumites
So I went to the irc channel at #xkcd-sucks to get some help:
(09:25:07 PM) person1: if you had to describe friday's comic with one word, what would it be?
(09:25:17 PM) rmason: look at me i'm person1 and i appeal to other people's narcissism out of my own laziness
(09:25:20 PM) rmason: DERP DERP DERP
(09:25:28 PM) person1: lol
(09:25:30 PM) person1: fuck you rob
(09:25:31 PM) rmason: the word is 'loathsome' btw
(09:25:33 PM) person1: you gigantic fatass
(09:26:07 PM) Sh0rtWave: Which one's that?
(09:26:15 PM) person1: the brain worm one
(09:26:28 PM) rmason: oh wait no it's GOOMH-bait
(09:26:30 PM) Sh0rtWave: One word?
(09:26:31 PM) Sh0rtWave: hrm
(09:26:31 PM) rmason: that is my word
(09:26:32 PM) Superbest: man, it's so meh I can't even find a word
(09:26:42 PM) rmason: i had a friend share it on google reader with a 'GOOMH'
(09:26:45 PM) rmason: i wanted to murder her
(09:26:47 PM) person1: ME TOO
(09:27:02 PM) The_Autodidact: is this that one friend that you hate for posting stupid stuff on twitter
(09:27:04 PM) Sh0rtWave: Presumptuous, is the best word I can come up with after "fucking stupid", but fucking stupid is two words.
(09:27:05 PM) rmason: no
(09:27:11 PM) rmason: this is a friend that i actually like
(09:27:18 PM) rmason: it made it all the viler
(09:27:46 PM) Superbest: I guess I could say meh, but it's even more meh than that word implies, somehow
(09:27:56 PM) rmason: ultrameh
(09:27:59 PM) rmason: megameh
(09:28:02 PM) rmason: MONSTERMEH
(09:28:12 PM) rmason: I am a huge fatass
I'm done.
also randall is in your head? how ORWELLIAN! I don't feel like this post is worth proofreading, so fuck you guys (again).


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Make your event one to remember with live music from Func On The Rocks. For more videos and clips, plus a full list of our extensive repertoire visit our music page.
No event too big or small!
Whether you're having a more intimate wedding or birthday celebration, large corporate event or festival, there is no end to the versatility of these highly experienced musicians. Available as a 6 piece band or with additional brass all the way up to our ultimate 10 piece depending on how much you'd like to be func-ified!
Song request..?
The first dance is one of the most important moments for any couple on their wedding day, and Func On The Rocks take great pride in being given the opportunity to share that moment. No matter what your music taste, there is no song that can't be done, all you have to do is ask!
Visit our NEWS! page for the latest news and updates from our hectic schedule of music, music and more music.
BOOK YOUR FULL ENTERTAINMENT PACKAGE NOW & SAVE £££'s!
Each booking includes our complimentary DJ playlist*, manned throughout the night and tailored to your individual music taste to keep your guests up and dancing into the wee small hours.
Do you have an event in mind? Click here to send us your information and we'll be in touch very soon!
* Standard package includes disco plus stage lighting, available any time between the hours of 19:00 – 00:00 (midnight). Optional extra hours are subject to additional charges. For full details of all pricing and packages please contact us for a no obligation quote.