Auckland and Waiheke Island

We arrived at Auckland Airport very excited. We had always wanted to come to New [...]

Worldwide LAM Awareness Month

June is Worldwide LAM Awareness Month (WWLAM)! Ten women contributed their stories for us to share [...]

How LAM impacts daily life

People who don’t have lymphangioleiomyomatosis (LAM) probably don’t understand what it’s like living with a [...]

Positive perspectives for women with LAM

Having lymphangioleiomyomatosis (LAM) is awful. Not only is the physical decline challenging, the psychological effects [...]

Advice for newly diagnosed women with LAM

I know first hand how scary it is to get a diagnosis of lymphangioleiomyomatosis (LAM). [...]


Being your own advocate

Being your own advocate and trusting your instincts is so important when you have a [...]

LAM community support

Being an active member of the lymphangioleiomyomatosis (LAM) community has really helped me cope with [...]


Symptoms of LAM

According to the LAM Foundation, the symptoms of lymphangioleiomyomatosis (LAM) can include: Shortness of breath [...]

Healthy living with LAM

Lymphangioleiomyomatosis (LAM) is a degenerative lung disease. As the disease progresses, one’s lung function decreases. [...]

Tips for traveling with LAM

Travel Breathe Repeat is a travel blog. One of the people traveling just happens to have [...]