Wednesday, June 29, 2011

My RA Bedroom...the ABC's of getting some zzzzzzz's


My RA Bedroom:

I think I picked this room first to apply my KISS principle to because it is one of my favorite rooms in my home and because I use this room so much.

There are several good blogs written on the best mattress to select when living with ra and rather then rehash that topic, I am providing you with the links below for you to check out yourself. But the short of the mattress matter is two types seem to be rising to the forefront with ra sufferers: the sleep number bed and the tempur-pedic mattress. Both of these beds sell adjustable electric frames which allow you to raise or lower the head of the bed as needed.  

Now you are probably asking yourself what type of bed does Deb own.  I am still using my mattress from almost ten years ago but I suspect that within the next two years I will be venturing down the mattress shopping isle.  I currently own a pillow top type that I paid over $1,200 for ten years ago. Mattresses can be expensive and I am trying to hold off for as long as possible.  I am not sure which mattress I would buy but I have had the opportunity to sleep on the tempur-pedic mattress for a few weeks. It was a little too hot for me. And I would have to check carefully on the sleep number bed as I have kitties. Kitties have claws and I am not sure how kitty claws would do on an air type bed. I am still up in the air on my decision.

I am going to cover pretty much everything else that might make living with ra easier for you in your bedroom. Call this my wish list for the most functioning ra room around.  But, just like medications, our bedroom must work for us.  Surround yourself with what works for your ra and your particular challenges or needs.


The RA Bed:

  1. Various pillows that contour to your body (maybe even a full length body pillow for those hard to sleep nights) but not so many that they overtake your bed. And you may want to consider a good support pillow for reading.
  2. Set of cotton sheets that are large enough for ra hands to easily make the bed (of course as I have previously written…if you can hire housekeeping help, by all means do it!). I say cotton because often we with ra sweat at night and for me the cotton has worked best with this problem. I love all things cotton!
  3. A lightweight summer cover like a quilt for the bed during the summer. Again I prefer cotton.
  4. A lightweight  comforter for the cold months (the key here is lightweight!) or an electric blanket if you prefer to snuggle under. The more layers you put on your bed, the harder it is to make the bed. I have an alternate down one in white as I have down allergies and down can be heavy.
Everything else in my ra bedroom:

  1. remote controlled fan
  2. flat screen tv mounted on the wall for easy viewing and a no strain neck position along with a dvd or blue ray player.
  3. A solid chair that you can use for sitting or when you need to put your shoes on. I prefer one with arms as they help me to get up and down.
  4. Dressers with big knobs. I use to have a dresser with handles but my fingers often got stuck in the handles. Knobs can be harder to grab but they work better for me personally…no more trapped swollen fingers.  If your current dresser does have tiny knobs you might want to change them out with bigger ones. Use what works best for you. And drawers that don't require two hands are always better then drawers that do.
  5. A nightstand with big drawers to fit all of my ra medications, rubbing creams, and pain patches on my side of the bed. Nightstands are great in bedrooms whether you have ra or not but I feel they are essential for people with ra.  Mine also has a nice shelf on the bottom where I keep my current reading materials. If you have small children in your home, you probably shouldn't keep any medications in your night stand where the webbies can get to them.
  6. Lamps with touch control.  I don't have these types of lamps anymore as I have kitties….you get the picture here. I do miss my lamps!
  7. Enough room on the side of your bed where you can leave your slippers on the floor. I must have slippers on my feet at all times when I am in my home. I have bad ra in my feet. To be honest I also keep a pair of sneakers at my bedside because some days my feet are too bad for slippers…I need the running shoes with the support on my feet before I get up and get moving at all.
  8. An outlet close enough to your bed to plug in your laptop computer so you can read my blog easily (just kidding)  and any other electric things like an electric blanket or heating pad. But be sure that the cord runs along the wall and doesn't lay across the floor which would make it a tripping hazard.
  9. No extra throw rugs anywhere in the room. Throw rugs tend to trip up people with  ra no matter how well taped down they may be.
  10. Have clear access on at least one side of your bed if you use a wheelchair. And there should be enough room to maneuver the chair easily to access the dresser and closet in the room.  A lower dresser will be needed if you use a wheelchair. And you may have to downsize your bed to accommodate a wheelchair if this is a new ra accessory for you. 
  11. Room enough on one side of the bed if you have a walker and room enough to maneuver easily around the room.
  12. If you have a cane then you may want to consider a way to ensure that it doesn't fall over when you aren't using it. Maybe an umbrella stand or if your hands are capable enough a fastener or hook on the wall to keep it off the floor completely.
For me ambiance is critical in my ra bedroom:

  1. Choose colors that will soothe you. 
  2. surround yourself with artwork that lightens your mood.
  3. be sure your windows have room darkening capabilities. Sleeping with ra can be difficult enough, having the sun blaring you in the eyes will just make it that much worse. Daytime naps are often needed with ra. And least we not forget. 
  4. a radio or cd player so you can surround yourself with your favorite music or a cd player with headsets at the very least.  
  5. I also have scent ports in my room that I fill depending on my mood. Scents can help to lift your spirits or calm your frayed nerves. There are also natural scents out there if you prefer.

But do keep in mind that if your ra room is made too comfortable, you will have your entire family wanting in on this new great ra retreat. Anyone say sleepover!



Additional reading:
Tips on Making Your Bed: Arthritis Foundation

Monday, June 27, 2011

The Blog Party Rocks on!

The party is rocking. I hear a song playing...Getting to know you...getting to know all about you.

Calling all ra-ers! Want your name up in lights! Want your story told....check in with Lyda. She is looking to feature you in an upcoming blog. What better way to spread the knowledge of ra...come on out on the dance floor and let the spotlight shine on you!

http://lydaclark.blogspot.com/2011/06/gettin-to-know-ya.html


Gettin' To Know Ya

Since I started this website, my favorite thing has been connecting with people from around the world who also have Rheumatoid Arthritis. I went from knowing maybe two other people who went through what I was going through, to a network of people all over the globe. I have never felt so at home, so comfortable, so able to open up with my new community of friends.

A year ago, I was uncomfortable discussing my health with anyone outside my circle of trusted friends and family. Once I started writing regularly and getting over my fear of opening up to strangers, I realized how great this whole idea was.


These are a few of my favorite things...blog party time!

My favorite blog things that is...so here goes! I hope you give them a try like I have already done. They are now part of my blog family and I hope they become blog family members of yours too!
So let's get this party started!

RA Guy Rocks! I am not sure which of his posts is my favorite one but this one is his most recent...I for one love his art work! And while you are there, buckle up and do take the ra roller coaster ride :-)
http://www.rheumatoidarthritisguy.com/2011/06/rheumatoid-arthritis-roller-coaster/
http://www.rheumatoidarthritisguy.com/2011/06/ra-guys-hope-unlimited-mug/

Rheumatoid Arthritis Guy is pleased to announce the release of his “Hope! Unlimited” mug, which is now available on Zazzle.com!
RA Guy's Hope Unlimited Mug
This mug was especially designed for all superheroes who are living with rheumatoid arthritis, including their friends, family members, and co-workers.
Hand drawn by RA Guy, the art work includes some of the most popular comic book images from his website. The white text on the blue sky is from his “About Me” page, which represents the first words that were ever published on his blog.
You too will feel like a superhero when you use this mug!
Help superheroes like myself overcome “Flare Incorporated” and reach “Hope! Unlimited”.
 RA Warrior...
http://rawarrior.com/santa-bring-her-a-rheumatologist-please/

Santa, Bring Her a Rheumatologist Please


Wanted poster: rheumatologist

Wanted: good rheumatologists

Sonya’s tweet brought me a smile. So much truth in so few words. Those of us with rheum diseases like RA need a good doctor the way most people need a reliable car mechanic. We might crash and burn without it.
This is short for two reasons:
1) I don’t have a long list of requirements. It’s pretty simple.
2) I want to hear about what you want or need in a rheumatologist!

Santa bring me a rheum Tweet

My list: rheumatologist wanted who…

  1. Performs joint examinations and accurately records medical history.
  2. Uses suitable tests for monitoring disease progression and to help insure safety with prescriptions.
  3. Stays up to date on current tests, treatments, and research.
  4. Does not try to use rheum factor lab tests or CRP the way endocrinologists use blood glucose tests, but asks patients about disease activity.
  5. Will fairly communicate with patients on an adult level without any type of abuse.
Treating RA is not easy and we know the field is changing quickly. Rheumatologists can learn more about RA by listening to patients and not scoffing at their symptoms, or rolling their eyes, or making rude comments such as “At least you don’t have nodules like some b@$%&* do!” or “Just get over yourself!” (Those are real recent comments sent by readers.)
Let’s boil it down to what really counts.

What do you want in a rheumatologist?

Note! I get lots of letters asking to help find a good rheumatologist. And this will only increase when the new Rheumatoid Patient Foundation site is opened. If you have a great rheumatologist, you can leave his or her name in a comment here to nominate him / her for the recommended rheum docs list. We are building a great list. We will ask if they’d like to be on the list and a patient’s name will never be mentioned.

P.S.....This is ABCsof RA here...anyone know of a great one in southeast region of NC? I am still a hunting for my great ra doc!
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RA: Ready for Action


Sunday, June 26, 2011


Water Exercise


When I was officially diagnosed with RA, I joined the YWCA and started attending water exercise classes there. I also had to go out and buy a swimsuit--for the first time in 15 years! Going to the YWCA is good for my ego, as I am among the youngest there (me, with my white hair) and am almost "thin" in comparison to some people.

I especially like the deep water exercise classes, where we exercise with the noodle. It can be strenuous, though each person adapts at his/her own pace. I really like it and feel better going to these classes.

When I can attend two consecutive classes, I feel really good about myself. However, sometimes two of the deep water classes can be too much for me. It works out best if one is in the shallow end and the other in the deep end, like on Thursday mornings when there is first a water yoga class followed by an exercise one.

Not having gone since Thursday, I am eager to start again tomorrow. Luckily, I do not work, because this takes up most of each morning.