硬皮病患者的生活。如何与硬皮病共存?

硬皮病患者是否可以过正常的生活?硬皮病患者应该如何保持乐观?硬皮病可能会影响您的日常生活,但您必须保持乐观。看看其他病患如何抱着乐观的态度与硬皮病共存

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Systemic scleroderma is a life changing experience for anyone. It often puts major stress on marriages as it is often has many "invisible" symptoms such as pain and fatigue. Many patients are finding that joining one or more support groups, both online and locally (where available) is a wonderful way to connect with others and get tips but also to help others by giving support and providing information about their own experiences with drugs or ealing with specific symptoms.

In my case, I made the unusual journey from being diagnosed in 1990 to now becoming an educator and published researcher. I also spend a couple of hours a day helping others, which I find very satisfying.

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