Please select all the ways you would like to hear from Travel Breathe Repeat:
You can unsubscribe at any time by clicking the link in the footer of our emails. For information about our privacy practices, please visit our website.
We use Mailchimp as our marketing platform. By clicking below to subscribe, you acknowledge that your information will be transferred to Mailchimp for processing. Learn more about Mailchimp's privacy practices here.
Information and stories about living with LAM (lymphangioleiomyomatosis) based on Sarah’s personal experience with this rare, chronic lung disease.
Hi my name is Bree and I live in the coastal town of Capel Sound [...]
June is Worldwide LAM Awareness Month (WWLAM)! Ten women contributed their stories for us to share [...]
People who don’t have lymphangioleiomyomatosis (LAM) probably don’t understand what it’s like living with a [...]
Having lymphangioleiomyomatosis (LAM) is awful. Not only is the physical decline challenging, the psychological effects [...]
I know first hand how scary it is to get a diagnosis of lymphangioleiomyomatosis (LAM). [...]
Being your own advocate and trusting your instincts is so important when you have a [...]
Being an active member of the lymphangioleiomyomatosis (LAM) community has really helped me cope with [...]
According to the LAM Foundation, the symptoms of lymphangioleiomyomatosis (LAM) can include: Shortness of breath [...]
Lymphangioleiomyomatosis (LAM) is a degenerative lung disease. As the disease progresses, one’s lung function decreases. [...]
Travel Breathe Repeat is a travel blog. One of the people traveling just happens to have [...]