The AddisonsDisease.Net Difference: We are the place to come for free meaningful lifetime support. Our members achieve victories in improved wellness and understanding of Addison's Disease through daily interaction with real people who live with this rare endocrine disorder. Our members always put each other first and have such wonderful words regarding this amazing family of such very special people: "I have been a member for several months now and wanted to thank everyone for thier advice and help. Like many members I may not reply to the e-mail very often, but I do read them everytime. The information I have gained through this group has improved my life tremendously. From the little things like taking your meds before you get up to the big things like dealing with a crisis this group has made a huge impact on my life. Thank you to everyone who takes time out of thier busy schedules to answer questions and give advice. Your contribution is appreciated and makes a difference." AddisonsDisease.Net was founded by someone with Idiopathic Primary Addison's Disease - Complete Adrenal Insufficiency as a place of unsurpassed meaningful support. We've seen the recent media frenzy linking Paula Abdul to Addison's Disease and the sudden but fleeting awareness it has brought to this once terminal disease. The AddisonsDisease.Net difference is that we are always here to support our members who have it or who care for someone that does. Our members cross all cultural, economic and every other imaginable boundary to come together as one family who grows in wellness and size each day. We hope all who have taken the time to read this take a moment to do their small part. We promise that it will come back to you many times over.

The AddisonsDisease.Net Difference:

We are the place to come to for free meaningful lifetime support. Our members achieve victories in improved wellness and understanding of Addison's Disease through daily interaction with real people who live with this rare endocrine disorder. Our members always put each other first and have such wonderful words regarding this amazing family of such very special people:

"I have been a member for several months now and wanted to thank everyone for their advice and help. Like many members I may not reply to the e-mail very often, but I do read them every time. The information I have gained through this group has improved my life tremendously. From the little things like taking your meds before you get up to the big things like dealing with a crisis this group has made a huge impact on my life. Thank you to everyone who takes time out of their busy schedules to answer questions and give advice. Your contribution is appreciated and makes a difference."

AddisonsDisease.Net was founded by someone with Idiopathic Primary Addison's Disease - Complete Adrenal Insufficiency as a place of unsurpassed meaningful support. Our founder has from day one and continues to have a daily presence in the community. AddisonsDisease.Net was created and thrives as a free service to our members from around the world and they always come first.

We are here to do our part to help our members improve their lives by connecting them to the deepest knowledge base of patient experience and understanding on adrenal insufficiency - Addison's Disease anywhere in the world. Patients, caregivers, doctors, nurses, media outlets, hospitals, healthcare organizations, pharmaceutical companies and the general public are invited and encouraged to spread the word about this growing family called simply AddisonsDisease.Net.

Way you can help?

Putting a link from your healthcare website to ours instantly makes your site more valued as you connect someone in need to a resource able to help that person who has Addison's, thinks they might have it or cares for someone who does. Once they reach us our members will take it from there and you will have made a real difference in someone's life.

We've seen the recent media frenzy linking Paula Abdul to Addison's Disease and the sudden but fleeting awareness it has brought to this once terminal disease. The AddisonsDisease.Net difference is that we are always here to support our members who have it or who care for someone that does. Our members cross all cultural, economic and every other imaginable boundary to come together as one family who grows in wellness and size each day.

We hope all who have taken the time to read this will take a moment to do their small part. We promise that it will come back to you many times over. learn more

Wishing everyone the very best of health.

Sincerely,

The Support Team
TELEPLEXUS®
www.addisonsdisease.net
A growing caring community

The information provided here should not be used for diagnosis or treatment. A licensed physician should be consulted for the diagnosis and treatment of Addison's Disease and all diseases. TELEPLEXUS, Inc. does not warrant that this information meets any particular standard or that it is free from errors.

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