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Hetlena PatientsLikeMe member with lupus

Newly diagnosed with lupus? Member Hetlena’s pointers for her old (newbie with SLE) self

What would someone who has lived with lupus (SLE) for decades tell her younger, newly diagnosed self? PatientsLikeMe member Hetlena (@TheLupusLiar), who was diagnosed with lupus in 1993, recently answered that question for us in the following personal essay reflecting on what she’s learned through the years…

“This isn’t the end. There are other things that can give your life meaning.” —Christine Palmer, Dr. Strange (2016 film)

In the 2016 movie Dr. Strange, a main character, Christine Palmer, captures how it feels to be confused, frustrated and hopeless – feelings I’m very familiar with because of SLE. The diagnosis of lupus can be mixed with pain, nausea, fever, swelling and all too many other symptoms and ailments combined. From the very beginning, it became more than I could bear – or at least so I thought. I felt targeted all the time. When I reflect on my feelings right after my diagnosis, I remember most of all that I didn’t feel confident.

If I knew then what I know now, I would…

Question everything

There was so much about lupus that I didn’t know about (and years later, there still is). Naturally, a diagnosis or the confirmation of one can come as a shock. Because of all the perplexing activity that happened with my body, I knew something was going on. Writing down questions about the pain would have reminded me to ask my physician and help shape the treatment path for my medical team to explore.

Asking questions also would’ve curbed my anxiety and desire for the doctor to just cure me. I would’ve been more open to the fact that my physician needs to question and test things, too. This would have saved a massive amount of time in the trial and error phase of my diagnosis.

I would also ask more questions about medications and treatments, rather than just swallowing the pill, literally. Medicine is not always medicinal. In addition to asking how a new treatment would affect my stomach and daily function, I would also ask how the medicine would affect my finances (and see if there is a generic of the medication). Now, I take the time needed to research recommended medications and treatments online. Many lupus patients have more experience with treatment plans, so I also read comments from patients in lupus forums like PatientsLikeMe.

Journal the journey

When my body was constantly going through discomfort, I would’ve kept a diary of what was happening, with as many details as possible about my symptoms. I would keep a record about what I ate, what I was doing, and even what was occurring around me during the heightened times of what I now know were flares.

Know that patience takes practice

Waiting on test results wasn’t always easy. Yet, what else was I going to do? I could keep hounding the medical offices, but it wouldn’t make the results come back any faster. Every step toward my diagnosis required patience for the people and process required to help me reach the most informed outcome possible. If I could go back in time, I would mark my calendar with appointments when blood would be drawn and also when the test results were expected to be back. Understanding that my medical team would need time to review test results would’ve helped me realize that waiting was inevitable. I know now that patience is more than a virtue – it is a lifestyle change.

Accept my new role (patient)

At first, I felt that solutions lay in my physician’s office. I viewed every doctor’s appointment as an open door to feeling better. That was not so. My visits became a revolving door of questions and tests. Not every appointment led me out of the maze. I was angry. I was upset. I didn’t want to accept the fact that the time and knowledge of the specialists was indeed worth a lot. After a change in perspective, I reflected on how all this personal process was a labyrinth of decisions – decisions that I took the lead on. I was the chief of my medical journey. As a patient, my perspective was my guide.

Talk to people

A diagnosis doesn’t mean it’s the end of your relationship with life. If I knew then what I know now, I would not be shy in sharing my confirmed diagnosis. Social media is not always the only outlet to therapeutically release the ups and downs of life. But it can help. I would share with my family and friends about my new limitations. I believe divulging my personal concerns early on in my diagnosis would have released a lot of stress that I didn’t have to internalize. Talking about things makes them less scary. Another person’s perspective can help you make sense of things that are going on with your health. It also makes you more confident in communicating your concerns.

Find the positives

The limitations of lupus that I thought were going to weigh me down actually became new ways of lifting me up. For example, now I pay closer attention to what I eat. I’ve added exercise and yoga to my weekly routine. I take the time to pack carefully for a trip instead of just throwing my stuff in a bag and going. Planning makes my health and trips go so much smoother than before I was diagnosed with lupus. But most of all, I get to look at my relationships more carefully. I found meaning in sharing my story with others. Helping others take a more positive spin on being diagnosed with lupus is both rewarding and challenging. But it’s so worth it!

I know now: acknowledging a lupus diagnosis is not an easy thing to do. It takes practice to be proactive instead of reactive, and the journey can be more comfortable with more experience.

1 comment

  • Diagnosed since 1997 I’m a warrior . I have my good and bad days but I fight for me, my kids and my grands they give me strength. I get out of bed when I just want to sleep, I pray because I need to be here for my family as long as God gives me breath.It’s not over until he says it is .be strong lupus warriors .