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 ECAA Brochure for New Patients
A new ECAA Information Brochure is now available here. The brochure tries to answer the major questions that the newly diagnosed patient may have. It is written in an easy-to-understand format and offers pointers to places to find more comprehensive information.
Information
Our site offers easy-to-read information on EC - descriptions of the disease, its diagnosis, staging, treatments, and other factors.
We also offer links to other sites that can help you to know more about the disease.
ECAA Membership
Membership of the ECAA is open to anyone. We are a very small organization that depends heavily on our members to be able to continue our work.
Please consider joining us and visit our Membership page for more details.
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Merchandise
Show your support for EC Awareness. The ECAA has caps, shirts, wristbands, and bracelets for sale to help you show your support.
  
Go to the Merchandise page to see what we have. You do not need to be a member to purchase.
Gifts and Donations
The ECAA is an all-volunteer 501(c)(3) organization. 100% of all gifts, donations, sums bequeathed, and monies from sales of merchandise goes toward the efforts of the association to raise the awareness of EC.
You can read more about our organization on the Gifts and Donations page.
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ECAA Newsletters
The ECAA newsletter, Swallow Tales, is published quarterly in January, April, July, and October.
 Swallow Tales publishes articles of interest to patients, caregivers, partners, and families. We try to keep the content relevant, interesting, current, and as lighthearted as the subject matter will allow.
Support
One of the main benefits that we can offer is support.
 The members of the board cover a wide range of the world of EC experience - current patients, survivors, caregivers, and so on. Any of us are only too eager to be contacted and offer help and advice as we can
Anyone else who feels that they would be willing to help in this way can ask to be added to the list of ECAA supporters.
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