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You are here: Home / Body / No Easy Fix

No Easy Fix

Evelyn Herwitz · February 25, 2025 · 11 Comments

So, here’s what I learned at my optometrist last week, with a thanks to all who expressed concern and good wishes:

My blurry vision is due to the fact that my eyes simply don’t make enough tears, the result of Sjögren’s Syndrome that I’ve had for decades. The relief I’ve gotten from using EvoTears, which form a moisture-trapping film over my eyes, is real, but not enough to keep my corneas truly healthy. So, especially in my right eye, which is more blurred, my vision is effectively analogous to looking through a dirty car windshield. This isn’t cataracts. It’s Sjögren’s. And there’s no point in updating my eyeglasses prescription until my corneas heal, because I can’t get an accurate assessment of any vision changes right now.

The other important fact I learned: The Restasis drops (standard treatment for dry eyes) that I use before the EvoTears are in a castor oil suspension. I need to wait a half-hour between the two eye drops, or I’m effectively trapping the castor oil in my eyes. This explains some of the irritation I’ve been experiencing. So, that’s an easy fix.

My optometrist gave me samples of a varenicline solution nasal spray, which I’ve used before, that stimulates tears, to see if this in combination with both eye drops will help. There are two issues with this approach: First, the spray helps, not not markedly, so far. Second, the nasal spray is outrageously expensive, available only by prescription, and not covered by my insurance.

So, I’m back to finding a way to tolerate the scleral lenses. He checked both lenses for me, and there are no scratches, so however I injured my eye a few months ago was some kind of fluke in the way I inserted the left one. I will need to keep the lenses in at least four hours a day, four to five days a week, to really heal my corneas and maintain them.

With six fingers in bandages right now, including that left ring finger still healing from a lost nail and an infection, that’s a challenge. So, I’ll just need to tough it out with the medications I have until I have better dexterity again. (As a side note, I’m typing with just my left pinky on the left hand right now, and somehow I’ve learned to type by touch and don’t have to look at the keyboard. So, that’s some progress!)

If there is any advantage from dealing with scleroderma and its sidekick diseases for more than 40 years, it’s this: I know my body does eventually heal from assaults like this. It just takes time and a lot of patience and vigilance. As the weather warms and my hands improve in their seasonal cycle, I should be able to master the lenses again and find the right balance. I’m grateful that I have access to excellent care and medications and the scleral lenses, even if they are difficult to deal with. The alternative is much, much worse.

Evelyn Herwitz blogs weekly about living fully with chronic disease, the inside of baseballs, turtles and frogs, J.S. Bach, the meaning of life and whatever else she happens to be thinking about at livingwithscleroderma.com. Please view Privacy Policy here.

Image: Unsplash+

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Filed Under: Body, Mind, Sight, Touch Tagged With: adaptive tools, body-mind balance, finger ulcers, Sjogren's syndrome, stress

Reader Interactions

Comments

  1. Rita says

    February 25, 2025 at 10:27 am

    It sounds like the best possible outcome!
    I have been on Ambrisentan for quite a while for pulmonary arterial hypertension.
    Not only is it working for PAH, but it is working well for my Raynaud’s. Thank God, it’s been exceptionally cold this winter here in Colorado.
    Sending prayers your way.

    Reply
    • Evelyn Herwitz says

      February 25, 2025 at 10:57 am

      Thanks, Rita. I’m glad to hear you’re doing so well on Ambrisentan. Hope it warms up soon there!
      Be well.

      Reply
  2. Patricia Bizzell says

    February 25, 2025 at 5:49 pm

    What a complicated struggle, Evie, I’m so sorry you have to endure this, I marvel at your endless inventiveness and staunch courage to deal with it all.

    Reply
    • Evelyn Herwitz says

      February 26, 2025 at 7:50 pm

      Thanks, Pat. 🙂

      Reply
  3. Patrice A Veazey says

    February 26, 2025 at 1:56 pm

    You are a tremendous inspiration to me> Thank you for sharing and doe giving us the path to healing!
    BTW, I use Neosporin (not triple antibiotic ointment) for any and all infections or open sores. I have had great results!

    Reply
    • Evelyn Herwitz says

      February 26, 2025 at 7:55 pm

      Thank you, Patrice. I also use topical antibiotics on my ulcers, with mixed results. Sometimes Mupirocin, which is a prescription level version of Bactroban, can be helpful, but I also find it can break down my skin. I have to be very careful with it. Usually, the only way I can really get rid of an infection is with Minocycline.
      Be well.

      Reply
  4. Patrice A Veazey says

    February 27, 2025 at 8:57 am

    Evelyn. You are an inspiration and your fearlessness is astounding. Thank you, all the way from Abbeville, Louisiana.

    Reply
  5. Patrice A Veazey says

    February 27, 2025 at 8:59 am

    I commented again because I didn’t see that my original comment made it thru. I’m kinda new to the blog system! Happy almost Mardi Gras! 😉

    Reply
    • Evelyn Herwitz says

      March 3, 2025 at 2:09 pm

      Enjoy the parades!

      Reply
  6. Jozelle says

    March 2, 2025 at 11:18 pm

    Thanks for sharing your journey Evelyn. I have a loved one with scleroderma and reading your post gives me insight and helpful tips. Praying for your wellness.

    Reply
    • Evelyn Herwitz says

      March 3, 2025 at 2:09 pm

      Thank you for your kind words, Jozelle. I hope your loved one is getting good medical care, and that you are taking care of yourself, as well. Blessings.

      Reply

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About the Writer

When not writing about living fully with chronic health challenges, Evelyn Herwitz helps her marketing clients tell great stories about their good works. She would love to win a MacArthur grant and write fiction all day. Read More…

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I am not a doctor . . .

. . . and don’t play one on TV. While I strive for accuracy based on my 40-plus years of living with scleroderma, none of what I write should be taken as medical advice for your specific condition.

Scleroderma manifests uniquely in each individual. Please seek expert medical care. You’ll find websites with links to medical professionals in Resources.

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