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.
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 [...]
While in Australia, I was lucky to meet women with LAM and other members of the [...]
Last year when I started talking to the LAM Foundation about this trip and mentioned [...]
The first woman with LAM I made on this journey was Sina. I met her [...]