Comments on: 6 Down, 24 to Go https://livingwithscleroderma.com/6-down-24-to-go/ Reflections on the Messy Complexity of Chronicity Mon, 27 Nov 2017 23:24:33 +0000 hourly 1 https://wordpress.org/?v=7.0.4 By: Evelyn Herwitz https://livingwithscleroderma.com/6-down-24-to-go/#comment-64029 Mon, 27 Nov 2017 23:24:33 +0000 http://www.livingwithscleroderma.com/?p=4956#comment-64029 In reply to Kathryn Riley.

Thanks, Kathryn! Best of luck with your HB treatments. I’m almost 2/3 of the way through and seeing remarkable progress. I hope you experience the same! Well worth the time and effort. 🙂

]]> By: Kathryn Riley https://livingwithscleroderma.com/6-down-24-to-go/#comment-64000 Sun, 26 Nov 2017 21:48:09 +0000 http://www.livingwithscleroderma.com/?p=4956#comment-64000 What a wonderful blog! I also have Scleroderma (CREST) and l am about to embark on HB treatments. It is great to hear that you are experiencing good progress. Your progress fills me with hope. Thank -You.

]]> By: Evelyn Herwitz https://livingwithscleroderma.com/6-down-24-to-go/#comment-63630 Wed, 08 Nov 2017 20:21:30 +0000 http://www.livingwithscleroderma.com/?p=4956#comment-63630 In reply to Kristine Washburn.

Thanks so much, Kristine! I just wish this therapy was more readily available for all of us struggling with scleroderma ulcers. If I could have done this last spring when the ulcers erupted, I would have been able to avoid all the struggle and surgery. I hope my experience helps to convince insurers that the benefits of HBO should be extended to all scleroderma patients!!

]]> By: Kristine Washburn https://livingwithscleroderma.com/6-down-24-to-go/#comment-63618 Wed, 08 Nov 2017 05:20:19 +0000 http://www.livingwithscleroderma.com/?p=4956#comment-63618 I’m sooooooo glad that the oxygen chamber is working. I’ve been praying for those fingers of yours. I know Raynaud’s related ulcers and complications are so painful and can feel defeating. I like how you view life while managing Scleroderma. Always living, learning, self advocating, and never giving up. You give all of us also living with scleroderma much needed hope.

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