Auckland and Waiheke Island
We arrived at Auckland Airport very excited. We had always wanted to come to New [...]
Jun
Worldwide LAM Awareness Month
June is Worldwide LAM Awareness Month (WWLAM)! Ten women contributed their stories for us to share [...]
Jun
How LAM impacts daily life
People who don’t have lymphangioleiomyomatosis (LAM) probably don’t understand what it’s like living with a [...]
Jun
Positive perspectives for women with LAM
Having lymphangioleiomyomatosis (LAM) is awful. Not only is the physical decline challenging, the psychological effects [...]
Jun
Advice for newly diagnosed women with LAM
I know first hand how scary it is to get a diagnosis of lymphangioleiomyomatosis (LAM). [...]
2 Comments
Jun
Being your own advocate
Being your own advocate and trusting your instincts is so important when you have a [...]
Jun
LAM community support
Being an active member of the lymphangioleiomyomatosis (LAM) community has really helped me cope with [...]
3 Comments
Jun
Symptoms of LAM
According to the LAM Foundation, the symptoms of lymphangioleiomyomatosis (LAM) can include: Shortness of breath [...]
Jun
Healthy living with LAM
Lymphangioleiomyomatosis (LAM) is a degenerative lung disease. As the disease progresses, one’s lung function decreases. [...]
Jun
Tips for traveling with LAM
Travel Breathe Repeat is a travel blog. One of the people traveling just happens to have [...]
3 Comments
Jun