|
A voluntary organisation dedicated to providing Support for Sarcoidosis sufferers
“our future is now“ |
|
|
|
Welcome to our site!!!
The Sarcoidosis Awareness Society (S.A.S.) has been created by sufferers who have knowledge and experience of how you feel and what you go through on a daily basis. If you are suspected of having or have just been diagnosed with Sarcoidosis you are probably feeling scared, worried, confused, lost and frustrated; all the things we felt when we first discovered the disease. We aim to provide you with as much information on the subject, guidance and support forums to help you gain the knowledge that we have all struggled to gain since our diagnosis. We are also starting local support groups in UK towns. So now you can discuss your experiences with others, enabling you to chat and learn from them for peace of mind and help you manage on a daily basis. 0 We are fully aware of the frustrations that you are going through with others attitudes including whilst dealing with health professionals. YOU ARE NOT ALONE!! The organisation offers support meet ups, allowing sufferers to come together in a relaxed environment to discuss the frustrations and problematic areas that we all face, along with providing the much needed emotional support. Feel free to browse our contents at your leisure.
Be sure to check out our campaign page for awareness and find out what we are doing to make things better for you!
(Please bear with us we are still under construction with many areas, which we will bring to you shortly)
Disclaimer: This website is provided for general information purposes only. The information contained within this site do not constitute medical or pharmaceutical advice, which should be sought from qualified medical and pharmaceutical advisers.
Copyright © 2010 Martine Caitlan of the Sarcoidosis Awareness Society. All rights reserved. |