It seems that people everywhere these days are having a difficult time to find the resources to keep going. Try to imagine, then, how it can feel to be diagnosed with a fatal and incurable disease on top of everything else. That's what happens to every single woman diagnosed with LAM (Lymphangioleiomyomatosis), who terrified and devastated looks anywhere for information, support and a helping hand.

All of us who went or are going through taxing and dramatic life challenges feel responsible to help people going through similar difficulties. We feel grateful to give back whenever we can, and know that no one can take anything for granted. I'm sure you feel the same.

No matter who you are, if or how LAM impacted your life, we hope you'd like to engage your friends to help women with LAM and their families to endure terrible uncertainty as a daily way of life, and still take manage to turn the proverbial lemons into lemonade.

Show you are relentless for cures.

Please fill out the fields below to send a message to your friends and family, encouraging them to volunteer or support The LAM Foundation and LAM Treatment Alliance.

Recipient Email Addresses: * One email address per text box
Your name	First Name	Last Name
Your Email: Please use your email address *
Subject:
	I've learned about a rare fatal disease called LAM (Lymphangioleiomyomatosis), and I want to try to help. You can find out more about it from The LAM Foundation website (www.thelamfoundation.org). One way to get involved is to volunteer time and help raise awareness for LAM. There are many different opportunities to reach out to the community, read this. Also suggest to our friends to donate. Will you please join me? Anything you and I do will positively influence those around us. We could bring hope and even champion for donations and gifts to make a difference in the lives of women enduring terrible uncertainty as a daily way of life. Thank you.