Would You Like Some WHINE with that Cheese?


How do you perceive “whining”? Never in my life have I coveted pity from others. I can’t stand for people to feel sorry for me! It makes me cringe … literally. I have been a strong woman in my faith, values, morals and work ethic. I’m proud to be a strong woman, but even strong women have their breaking point and RA was mine.  In the past, you could present a problem to me and I was action oriented looking for a solution to get it fixed and out of the way so I could move on to the next task at hand. You can’t fix RA which lends to frustration. Frustration vented sounds like whining. That is when I realized that is how the chronically ill get labeled as whiners. Unfortunately that label can start right in your own home, the doctor’s office, in your church, or place of employment.

Why do people whine? Bottom line: because they are not being heard and/or their needs are not being met. Unfortunately, that combo is prevalent with those suffering from rheumatoid arthritis. Why?

  • Lack of general knowledge about the disease among the public, your first contact medical team, friends and family. Grass root efforts to promote a name change from rheumatoid arthritis (RA) to rheumatoid disease (RD) or rheumatoid autoimmune disease (RAD) have been slow in coming. By continuing to have the word, “arthritis” in the name of the disease folks don’t realize that arthritis is a symptom of a bigger disease and limit its effects on the body. In fact others tend to think of RA as a version of arthritis due to aging (osteoarthritis).
  • Inadequate management of the symptom most bothersome to the patient: pain. Pain is what drives the rheumatoid patient to the doctor, but it’s not the primary focus of the rheumatologist who has been taught that if you prescribe the correct drug cocktail to halt to progression of disease the patient’s pain will improve and the patient has a chance of remission. I’ve not once heard of a patient seeking a rheumatologist because her finger is growing crooked! No, it’s because it hurts like HELL! Until rheumatologists change their focus on first getting the pain controlled, then looking at these long term treatment plans which are a shot in the dark (I’m going on 5 years with unchecked disease) then the patient/physician relationship will be compromised and synergistic solutions will be lacking.
  • Presumptions of others: you don’t look sick therefore you must not be sick.
  • Financial burden. When a biological agent costs in the thousands of dollars per month this puts a hardship on socioeconomic status, a burden on the family, and a preconceived burden on the public as one falls into disability.

If you know someone who has RA or is chronically ill, please try to look beyond the ” whine factor”  if indeed someone is whining because underneath is a person who is hurting both physically and mentally, just wants to be heard and accepted not necessarily fixed, and who needs others to at least try to understand. A little compassion goes a long way. Consider how you’d feel if life as you know it was yanked away from you because you became sick and try to approach your chronically ill loved one with that type of empathy.

If you are the one doing the whining, then I say:

  • Try to pick one or two people in your life to truly confide in and with whom to share your struggles. Getting your need to be accepted and heard met is key to decreasing the whine factor.
  • Be open-minded. It’s easy to develop a callous toward solutions when you’ve been told that XYZ cream, diet, exercise program fixed so-in-so. As a nurse and a patient, I can’t turn off 16  years of nursing education and practice. I try to give my fellow RA’ers a hand up by sharing my medical training when asked or I hear a whine. A whine is a need. Not all respond favorably. If someone goes to the trouble to help you when you’ve presented a need, please don’t cut them off at the knees. Instead see it as a blessing that at least that person cares enough to try to help.
  • Communicate your needs to your medical team and take control of your medical care. You are paying them for a service and if your needs for this service are not being met, then consider hiring another team.
  • Don’t allow your emotions to control you. Refrain from punching someone in the face when they ask literally or figuratively, “would you like some whine with that cheese?” and instead use it as an opportunity to reach out to someone by expressing yourself: “I’m sorry you feel as though I was whining. I’m going through a rough time right now and I could use some help,” then don’t be afraid to name the type of help you need: a hug, prayer, time together, back rub, comfort, a ride to the doctor’s office, etc… People become deaf toward whining, but are quick to respond to meet a need if they know what that particular need is, especially if they care about us. We only have to ask.
  • Be wary of bitterness. Slight after slight from others begins to become a brick wall where you start to close yourself off and categorize everyone as the enemy.  There is a difference between what is perceived as whining and what is pure venom.
  • Smile more. Try to find some joy in the simplest things by counting what blessings you do have instead of focusing on your have nots. For a while I fell into a slump of counting have nots and it was harmful to my attitude and outlook on life. Feeling sorry for yourself just doesn’t help a thing. Each person can find at least one thing per day to be thankful for even if it’s as simple as the sunshine on your face.
  • Know that you are not alone. There are support groups for RA patients online and demographically.
  • Trust in God. Even if there isn’t a single soul in your life that cares, God cares. Pour your heart out to him. He is always with you and he always listens. I’ve prayed for a cure for 5 years, but I’m not discouraged because I know if I’m not cured in this life I will be in heaven. My faith gives me a peace and hope in my heart.

Note: If you are newly diagnosed it’s perfectly fine to whine and carry on, scream, cry, beat the pillows but after a while you need to begin to educate yourself, take charge of your medical treatment and be a participant in your care. Do not allow yourself to wallow in your emotions. Try not to strike out against those closest to you in anger. You might find a blog I wrote about the grief associated with RA last year a helpful start.

Would I like some whine with that cheese? Why, yes please! A little compassion for a start. 😛

2 responses »

  1. Great blog!! i just found you on pinterest. (i just commented that I had sjogrens also) I can’t stop reading what you’ve written. I’ve had RA for 40 yrs and have never before found someone who really gets this disease as well as you do. I am also a christian. I can’t imaging having done all this on my own. I just had my 32nd surgery..knuckles replaced for the 4th time. Fortunately this time I picked the right surgeon who did a spectacular job. So grateful. Just 5 weeks out and I have a fully functioning hand. In the past it’s taken 3 months. Anyway, there’s so much I could say, but will not for now..i’ll continue reading your blog for sure. All the best to you, Sharon

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