Stories showing the importance of second opinions have been popping up in the media and on PatientsLikeMe. Check out the recent news headlines, hear a remarkable story of a PatientsLikeMe member who received a life-saving lung transplant after getting a second (and third) opinion, and share your own experience of piecing together your health puzzle.… Continue reading Life-changing second opinion stories: “I decided to get a second and third opinion…”
Tag: tips
10 hot weather and sun-safety pointers for people with lung cancer
On PatientsLikeMe, nearly 7,000 members are sharing their experiences with lung cancer. The dog days of summer have arrived, so we’ve rounded up some tips for handling the weather’s impact on breathing troubles and the side effects of chemo, radiation and surgery. Hot weather tips for people with breathing issues The American Lung Association reminds… Continue reading 10 hot weather and sun-safety pointers for people with lung cancer
Wheels up! Tips for traveling with a health condition
Got summer travel plans? For many, hitting the road with a health condition can take some extra planning, so we’ve gathered tips and tricks – from the PatientsLikeMe forums and beyond – to help you prepare for smooth sailing, start to finish. Before you go Bring a buddy. Traveling with someone – whether a spouse,… Continue reading Wheels up! Tips for traveling with a health condition
Bright ideas: Members share 7 head-to-toe tips for sun safety with lupus
With summer just around the bend, we’ve rounded up PatientsLikeMe members’ sun-safety and photosensitivity tips for people living with lupus. Photosensitivity is increased sensitivity to sunlight and other sources of ultraviolet (UV) light, sometimes causing a rash or other skin reaction. On PatientsLikeMe, thousands of people with lupus say they’ve experienced photosensitivity – more than… Continue reading Bright ideas: Members share 7 head-to-toe tips for sun safety with lupus
3 energy-saving tips for people with lupus
Fatigue can be a big deal when you have lupus. About 43 percent of PatientsLikeMe members with systemic lupus erythematosus (SLE) who are tracking fatigue as a symptom say that it’s “severe.” A rough day can feel like “walking through knee-deep water,” notes one member. Here’s a roundup of energy-saving tips from a few different… Continue reading 3 energy-saving tips for people with lupus