Tuesday, May 31, 2011

My Happy Tool Kit

What makes me smile…

It is so important with any chronic illness that we smile. And anything and everything (legal of course) should be employed. Gather yourself an arsenal of happy tools that you can pull out on those days when you just plain don't feel like smiling.

Here is some of my toolkit:

Her music just makes me smile every single day. She is a regular with my morning coffee and my afternoon tea...



I can't help but smile with him....




We have flowers in our yard.  Until I pick them all. And if I can't do the cutting on a particular day, my hubby is sweet enough to help me.  Did you know that my eyes and nose smile too...


And my stomach loves to smile...


Other times, the smiles just happen...



Or I may have to go outside to find a winged smile...




Or a crabby smile.




And there are times when driving is necessary to bring on a smile...



Sometimes I go online to smile...




I am always collecting new tools because I know I am in this for the long haul.  I want the biggest arsenal, the largest tool kit that will keep me smiling. I hope you start collecting your tool kit too!

Wednesday, May 25, 2011

The Cost of RA


There are some days I get so angry. I can't help but get angry. I have been in this body for twelve years now and still no cure. Heck, not even any real relief for more then an hour here and an hour there. And who am I kidding, I don't ever remember being completely pain free for the past twelve years. It is just a question of degrees. Is the pain barely manageable or not manageable at all…degrees indeed.

So I can't help but get angry sometimes. Angry at the fact that I got this disease in the first place. Angry at the fact that anybody has to get ra. Angry that ra exists at all! 

But what I am most angry at, is that there is no cure for rheumatoid arthritis. And why not?  I find it so hard to believe that with all the money that has been spent on research and the fact that this disease has existed since the caveman, that no one has come up with a cure. 


Do they realize the cost of ra and the return on investment they will receive if they truly find a cure?

And so I set out on my mission to calculate the cost of ra.  I calculate the cost of ra not to show how many dollars are spent by patients but rather what pharmaceutical companies will loose if a cure is found. 

Cost of ra for 1.3 million people (number taken from national institute of health currently diagnosed with ra) x $60,000 ($23,44l + $31,931 + $123,661 / 3) x 20 years of treatment (this 20 years is a guesstimate on my part as I couldn't find any study to use for this number) =  $1,560,000,000,000.00

OK, I think you see my point here.

This doesn't include the cost of surgeries, assistive devices, vitamins and loss of income by patients let alone the pain of ra and it's emotional cost to both the families and patients involved.

And from this calculation,  I suspect why no cure has been sought…it is tragically the cost of ra.

It is definitely about dollars and definitely not about sense!

How do we change this?

Pub med.gov  source used: Financial cost of early rheumatoid arthritis in the first year of medical attention 


Monday, May 23, 2011

Heigh-Ho, Heigh-Ho It's off to work we go...Part 2

The logistics of staying gainfully employed with ra isn't just knowing the "hard facts" of the law or the fine print in insurance polices. It also involves your ability to get up at all and to keep moving. And we all know that with ra, just doing that can be impossible at times.

Even to this day, I still use many of these hints to help me get going or to keep me moving.  As with all things ra, what works for me might not work for you. All I can offer is the hope that maybe one of these tips will help you in some way to get to whatever it is you want to do. Even if it isn't a job.

After being diagnosed with ra, I was forced to set my alarm several hours earlier. Why you may ask (although I am suspecting you may already have guessed)? To take my medications and give them time to kick in before I had to get out of bed.  My ra kept me in such pain, early on, that I had no choice. If I didn't make sure that all my medications where fully working, I couldn't put one foot on the floor. And I was desperate to keep my job and to keep going.

Ahhhhh...the bliss of water. Yes, the joy of standing under a hot shower to loosen up those oh so stiff joints. A good hot shower in the morning definitely got me a tad bit more revved up. But it does add to the prep time. I also always picked out my clothes * the night before (as well as my children's) and prepped all of our lunches. I purchased a timed coffee maker so I could prep the coffee the night before as well. This way, coffee was freshly brewed and waiting for me.

Breakfast usually consisted of cereal, oatmeal or possibly quiche (if I had previously double batch cooked). I also tried to keep fresh washed fruit available.

Guys you are so lucky! Ahhhhh...the dreaded hair and makeup. For this I usually pulled my hair back into a ponytail and I was pretty minimalistic with the makeup. A touch of eye shadow, mascara, rouge and lipstick did it for me. Back when I was working they hadn't come out with Bare Minerals which I swear by now. And for those that insist on blow drying your hair, there are blow dryer devices that some swear by (a stand of sorts so that you don't have to hold the blow dryer in your hands).

My son had the job of clearing the table and stacking the dishwasher while I gathered my daughter, 7 at the time, to walk her to the bus stop. My son walked to high school on his own. He was 17 at the time of my ra diagnoses.

Next I headed onto the 5 freeway running between Valencia and Burbank, Ca.  At that time, I owned a Sabb with a stick shift. Needless to say, one of the very first things I wanted to do was get a car with automatic transmission. We couldn't afford one at the time. Oh how I wish we could!

I know that one of the most frustrating things for me were doctor appointments. None of the rheumatologists in the area stayed open past 5pm. Why? Don't they realize that patients work? Don't they realize how difficult it is to juggle a job, child care and getting to their offices for followup visits, lab work, etc.?  I was lucky in the sense that I could play around with my start and finish time at work. Not flex time per se but something like that. Unfortunately, when I did switch my hours I also had to juggle the care for my 7 year old. My husband worked 24/7 and I swear during those years I was a single parent. Ironically, this practice of closing the doctor's office at 5pm still seems to be prevalent.  And if their office is open past 5pm, it is almost impossible to get an appointment because so many people need later hours. Duh! Hint to rheumatologists or any doctor for that matter!

Think me crazy if you will, but I often went out in my car for lunch to take a nap. I used the excuse that I needed quite time. Truth be told, I was exhausted and needed to sleep. I had a portable alarm clock. We have cell phones now with alarms that will work just fine. And my car was parked in a safe area where I didn't have to worry.

My cubicle, or office, was as ergonomic as I could make it.  I also would get up and stretch, walk around, find any excuse to move every hour so I didn't become like the tin man stuck in my seat. I even kept chemical hand warmers in my desk drawer. These are usually used by hunters for frigid weather. I used them to ease the pain in my hands when they were at their worst.



Twelve years later, I tend to prefer ice packs on my hands and wrists. You may want to rotate between the two (heat and cold) depending on what works best for your individual relief.

Driving home was always a challenge for me. A big challenge because I was so exhausted by then I feared falling asleep behind the wheel. I kept the a/c pumped up and the music pretty loud. I also would sing, talk to myself and yes, tap my face at times to keep awake. And of course, I always had that extra caffeine boost before I left work.

Once home, after hugging the kids, I would crash. Literally. From the sofa I would help with homework or take a nap.

Dinner was usually me reheating something I had double batched cooked from the weekend. And yes, at times I did bring food home from a drive thru or order pizza delivered. We gotta do what we gotta do to keep working.

In hind sight, I wish I had hired a housekeeper. I kept telling myself we couldn't afford it and we probably couldn't. Even one day a week or one day every other week would have been a immense help.  My children have always been very helpful and pitched in all the time but having someone to do the laundry and change the beds would have been such a relief. If you can afford it, do it.

And my last tip for the day...


* For women's business clothing I highly recommend the pant suit. I always tried to buy clothes I could wash as we were tight on money and I have a problem with dry cleaning smells. But if you can afford dry cleaning, by all means buy clothes that require dry cleaning. That is one less chore you have to take on. I also purchased business shirts that required no ironing. For me it was either a wrinkle free business shirt, a shell type blouse (used on days when I couldn't button a thing) or turtleneck in the colder weather. And always...flat shoes. After ra I could never wear heels and even on my best day, my feet just couldn't handle them. The "best shoes" for ra feet needs to be an entire post of its own :-)  We women sure do love our shoes!

So the short of this post is:
* Be sure you let your meds kick in before starting your day
* Take a shower in the morning if you can to loosen up those joints
* Keep breakfast simple
* Use a timed coffee maker so you can prep the coffee the night before
* Keep hair styles simple and consider makeup that has dual purpose
* Buy clothes that don't require ironing and have as few buttons as possible
* If possible, improve your work environment to accommodate your ra
* Use heat and/or ice to relieve joint pain
* Drive a car that is easy on the joints (automatic transmission number one on the list)
* Hire a housekeeper, lawn care, child care help...whatever help you can afford to keep your job
* Find a doctor that has evening hours or one that fits your schedule not theirs
* Order in, do drive through (until your medications allow you to cook more) or double batch cook
* Divvy up the chores and responsibilities among family members (you are family and should share the responsibilities)