Receiving a new diagnosis can be a life-changing experience. Some people feel like receiving a new diagnosis is validating, because now you have a name for what was giving you pain.
Other people feel the opposite way, and it simply leaves them with more questions. Google becomes their best friend (or The Mighty) as they scramble for answers about what this condition means for their lives, lifestyles, loved ones, their present, and their future.
We asked our chronic illness community “What advice do you have for someone who is newly diagnosed with CFS?” Here are the words of wisdom that they had to share: Go at your own pace “I would say to pace yourself.Read more on themighty.com