PRINCETON, N.J., June 9, 2009 –
1. What is AddisonsDisease.Net?
AddisonsDisease.Net is the largest and most effective support resource in the world for those living with Addison’s Disease and their caregivers.
2. Who Founded AddisonsDisease.Net and why does it matter?
AddisonsDisease.Net was founded by someone who nearly died from undiagnosed Addison’s Disease and was ultimately diagnosed with Primary Addison’s Disease – Complete Adrenal Insufficiency. Our founder has experienced the uncertainty of continued survival through such events and symptoms including hypovolemic shock, adrenal crisis, collapses at home pre-diagnosis, uncontrollable vomiting and diarrhea, hypotension, dizziness, intolerance to cold, muscle pain and aches, darkening of the skin, mouth sores and intense salt cravings to name some. Read More at http://www.teleplexus.com/8_Questions_For_AddisonsDisease.Net.html
3. Why was AddisonsDisease.Net founded?
AddisonsDisease.Net was founded to connect those who live with Addison’s Disease and those who care for someone with the disease to one another. Through member interaction, which we call learning through sharing, members live better lives with Addison’s Disease by being able to communicate with one another. Read More
4. Can caregivers become members of AddisonsDisease.Net?
Caregivers play a vital role in patient health and may freely join the community. AddisonsDisease.Net has many caregivers from all over the world; in fact, many take the time out of their busy schedules to let their fellow members know what AddisonsDisease.Net means to them. Here now in one of our caregivers own words as shared with the members of AddisonsDisease.Net. Read More
5. Will my wellness improve if I join AddisonsDisease.Net?
Many of our members experience profound improvements in their wellness as they interact with their fellow members. Many have formed powerful and meaningful bonds with their fellow members. Living with Addison’s Disease demands constant attention to a patient’s well-being and the members of AddisonsDisease.Net are right there for one another side by side in their journey together.
6. Where are members of AddisonsDisease.Net located?
AddisonsDisease.Net has members throughout the United States, United Kingdom, Canada and from such places as Sweden, Mexico, Poland, Romania, Australia, United Arab Emirates, New Zealand, Hungry, Iraq, Ethiopia, Italy, South Africa, Lithuania, Croatia, Ireland, Israel and many more countries around the world.
7. I’m a newspaper, television, web reporter or other media outlet, so why should I write a story about a rare endocrine disease? Read More
8. Why does someone need AddisonsDisease.Net in addition to a doctor?
AddisonsDisease.Net is the perfect companion to qualified medical care. The diagnosis and treatment of Addison’s Disease is only to be done by a qualified, licensed physician; however, the members of AddisonsDisease.Net are there to help. AddisonsDisease.Net has members just diagnosed to living with the disease for many decades. Read More
Fellow members regularly share with one another how AddisonsDisease.Net has effectively changed their lives: http://www.addisonsdisease.net/addisons.html.
For more information on AddisonsDisease.net, email .
Contact:
Jerry Butler, Teleplexus, Inc.
1-800-875-9130
http://www.addisonsdisease.net/
