The Scleroderma Chronicles: Updates from the Sclero Front

It’s spring here in Colorado. The first baby bunny appeared this week, and the plants in the yard are starting to burst out in green buds. The roses are looking like they are going to do really well this year (except for that one that the bunnies ate…) and there was a huge outbreak of my little bulb flowers in the front garden. I have new cushions for my patio swing, and I sit in the sunshine, reading and drinking my morning latte, every warm morning. On chilly mornings I wrap in a favorite shawl and stay out with the cats as long as I can. The first grasshoppers of the year have arrived for the cats to chase, and the air is filled with birdsong. There are even blue jays!! Good days.

The phlox in the front is looking great!

A couple of day have been so warm I couldn’t stay in the sunshine long and I’ve had to deploy the umbrella shade. Then, the next day, there may be snow. This is spring in Colorado: rapid changes and big temperature swings. The same is true for the barometric pressure; look at what happened this week.

My emotional stability has been a little like the air pressure the last couple of weeks as I’ve gone through a round of testing and doctor’s appointments. I was very upbeat when I went in to get my blood draw to check my iron levels, and the bone density scan last month was just routine. I mean, I’ve been feeling soooo much better: more energy, sleeping better, more mentally alert and even my appetite has improved. Suddenly my gut doesn’t hate me, and I am getting out of the house more. I went to my knitting group for the first time in months! I was positive that my test results would reflect the improvement.

Not so much. After weeks of eating iron-rich foods and downing my iron supplement there was absolutely no change in my test results, and in fact, the test that measures the concentration of hemoglobin in individual red blood cells (MCHC) got worse. Seriously? The only gain was one value of 25.5 that went up to 25.6; still too low. After all that red meat, salmon, iron pills, avocado, and spinach all I got was 0.1 improvement? Kind of disheartening as this means that I have to have some invasive testing to see if I’m bleeding in my stomach (it’s a scleroderma thing), and I don’t think my doctor will put it off much longer. (It’s called watermelon stomach) (fabulous) (of course this is rare) (my zebra self is not happy).

Then the bone density scan results arrived. I have somehow developed a fairly serious case of osteoporosis in a short time span; the report says to start immediate treatment. Then I did some googling and found out that the diuretic that I take can cause osteoporosis, and I absolutely shouldn’t have been taking it because I have a strong family history and I’m kind of high risk. (Of course I am) (I stopped the diuretic) (now my feet are swollen) (my zebra self is crying).

I have to be honest. I was kind of crushed by the bad news that I absolutely did not expect. Then I mentally slapped myself around, did my exercises, potted some lavender plants, and went shopping on Amazon for some cheer-me-up jewelry. Just what I needed to pull myself together. One day at a time, right? I already have more than my share of challenges, so I shouldn’t waste any energy on things that haven’t happened yet. Next week I have an appointment with my internist, and we’ll work out a treatment plan for the osteoporosis and next steps for the anemia. (I took another iron supplement) (my inner zebra has pulled itself together again) (the zebra wants to point out that its lips aren’t as blue as they used to be).

I also pulled out the La Prairie sweater and knit steadily through the sadness until the body came off the needles. Gosh. It looks really nice so far. Something has gone right this week…

Today I woke up to a snow/drizzle mixture that was too unwelcoming for even Mateo to go out on the catio. All my joints hurt, and my muscles weren’t sure if they were going to play nice either. Of course, I had to drive across town to get lung testing and a sit-down appointment with my pulmonologist to go over all my results. I put on my cute Weekender Crew sweater, wore my new “in your face, scleroderma!” jewelry, and headed off for the testing. It hurt to breath as I walked into the building. I convinced myself that it was just the cold air; after all, I feel pretty good, and I was overdue for some good news.

The lung testing specialist is now my friend. We laughed and talked and caught up as she got me ready for testing, and then I breezed through all the parts of the pulmonary function testing and the 6-minute walk test. Every single result was cause for celebration as Stephanie (my technician) became more and more excited with the little graphs and data appearing on the computer screen. “This is better!” she kept saying. By the last test she was practically jumping up and down with excitement. “This is great! This is great! she crowed as she walked me to the exam room to see my pulmonologist. “I’ll let him know that you are here.”

I love this pulmonologist. He is the doctor who first listened to me and picked up on the fact that I had a hole in my heart and pulmonary hypertension. He held my hand and told me I could cry when my interstitial lung disease was first diagnosed. He has always been the doctor who was most honest with me; he told me last year after the tide had turned that they hadn’t been sure I would make it a year. He supported me when I halted the anti-fibrotic drug due to quality-of-life concerns. Today he was all smiles as we went over the results and my exam. My lungs have maintained on the scans. I have regained some lung function. The decision to halt the drug was the right one; there is no obvious sign of fibrosis right now. This is the best possible outcome right now; everything that he hoped for. I was the last patient he saw today, and he was pleased to have such a good one. “Best appointment of the day!” he declared as he walked me out. We were both enclosed in a bubble of joyous happiness as we walked.

I took this picture outside the building.

Outside the clinic the parking lot was almost empty. The cold drizzle was steady, the sky was full of sad lumpy grey clouds, and the gloom of early evening was creeping in. Around the building some ornamental trees were just beginning to open their flower buds, but in the shelter of the courtyard on the south side, the sunniest location, one tree was covered in blooms. Kind of a metaphor for the last couple of weeks. Sit in the sunshine and bloom, no matter what is going on in the world around you.

On the drive home, in my mind, my zebra self was dancing for joy.

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Author: Midnight Knitter

I weave, knit and read in Aurora, Colorado where my garden lives. I have 2 sons, a knitting daughter-in-law, a grandson and two exceptionally spoiled kittens. In 2014 I was diagnosed with a serious rare autoimmune disease called systemic sclerosis along with Sjogren's Disease and fibromyalgia.

17 thoughts on “The Scleroderma Chronicles: Updates from the Sclero Front”

  1. I DO ‘like’ this – in fact, I love it !!! By all the gods, Marilyn, it’s a joy to read news like this !

    I read this quote not very long ago:

    “They say a person needs just three things to be truly happy in this world: someone to love, something to do and something to hope for.” And you have all three !!!

    Right now, you are truly happy. :)

    1. I am really happy, which is amazing after the sad little body blows of the earlier test results. It isn’t all that often that a person gets a jubilant day in a doctor’s office. 🙂

  2. Love the positive news and the lung tester and doctor who gave it. Also love the new jewelry. That last photo is a redbud tree, state tree of Oklahoma, where I’m from. I have one in my front yard that’s really doing its bloomin’ thing right now. Your phlox is looking pretty spectacular too.

    That barometric chart is kinda crazy. It certainly gives a great picture of what our weather has been like.

    1. Stephanie is just amazing! I told her how frustrated and upset I was with my care a few years ago and she went into my chart, read my test results, and then booked the first appointment with my current pulmonologist. Right there while I was getting my pulmonary function test done. I learned an important lesson that day: ask the professionals who deal with the doctors and patients who would be good in your specific area of need, and they will steer you clear of the lemons and give you the names of good, competent doctors. I’ve really hit the jackpot with my current pulmonologist and the team around him; they all just exude competence, and it is clear that they are a collaborative operation. My pulmonologist is a critical care specialist and was just pounded during Covid. I think that is why my good turnaround was such a happy end of the day for him.

      I just checked the barometric pressure again; there is another big drop on the way. Got to love these systems!
      Redbud! I have been wondering what that tree was. I just love it! I have family in Oklahoma, and I used to visit them in Pawhuska. We lost touch after my parents divorced, but I bet I saw some of those trees there and I didn’t remember.

      1. Competent, caring healthcare providers are worth their weight in gold. (I might be a little biased because my dad was a doctor)

        Was kind of weird this evening watching snow fall through the branches of my redbud. I hope it doesn’t get cold enough to zap the blossoms.

  3. Great news – so happy for you. I looked out the other day and my Phlox is blooming too, though not as gorgeous as yours!

    1. It is great news. I was slammed hard with the body blows of the earlier test results, but this more than offsets those results as the lung disease (it’s called interstitial lung disease associated with systemic sclerosis: SSc-ILD for short) is the leading cause of death in scleroderma patients. To see it paused and some of my lung function restored is just fantastic! He thinks that the diuretics helped with that, so I need to get on another one pretty quickly.

      My rose bushes are just covered in new growth, so I am looking at a great summer ahead. Usually they grow back from the root, but this time the stems are all still green and bristling with new leaves. Yay!! Let’s hope there isn’t a serious cold snap, but I think that it’s getting to late in the year for that.

    1. Who knew that anemia would cause so many problems! I am pretty sure that the iron is working, but not fast enough to keep my doctor from ordering those tests. On the whole, it is good news, and yesterday was a great day!

  4. I’m delighted by all the good news – and so respectful and… inspired? (urgh it sounds so saccharine) by your ability to feel your feelings but not dwell in them. You got some treats (always a good choice) and then you got on with things. Not everyone could do that.

    1. Thank you. It isn’t all that often that the walk out of the treatment area with your doctor has a sense of jubilance. As for the rest, I do try to acknowledge the validly of my sad reactions to bad news, but it is important for me to face down the monster, acknowledge what is happening, take appropriate action if there is one, and then put it into a mental box so I don’t have my life taken over by these things that are happening that I can’t really control. The truth is, I do become immobilized and unable to *make that phone call* because I’m not ready to handle bad news, but lately I’ve been doing better with that. Yay, iron!!
      ps: my doctor told me this time to not fall prey to “imposter syndrome” and to remember that my take on what is happening is almost always valid and accurate. I love this doctor!!

  5. Bummer about the iron – I hope they can get you on the right track (whatever that might be) to help with that and your osteoporosis. BUT! I am THRILLED at the info about your lungs/breathing. I hope that you high-fived everyone in your doctor’s office and I hope that continues to be the case for you!

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