Achalasia Foundation - Martin Mueller IV Achalasia Awareness Foundation

06/23/2024

We have new items in our store! If you would like to get a wristband or a t-shirt, please go to the following link to order today!

https://www.achalasiainfo.com/shop

Your purchase helps support our foundation in the research and awareness of Achalasia. Thank you!

06/22/2024

With The Society of Thoracic Surgeons (STS) – I just got recognized as one of their top fans! 🎉

06/16/2024

Today we recognize Achalasia as a rare autoimmune disease. The Martin Mueller IV Achalasia Awareness Foundation is our voice for advocacy and support. The foundation was just recognized by the Society for Surgery of the Alimentary Tract (SSAT) for the 2024 SSAT Public Service Award. We will continue to work hard for support, advocacy, research and help connect patients with doctors. We wear the “A” green and proud. Help support the foundation today by posting something green.

05/30/2024

With Global Genes – I just got recognized as one of their rising fans! 🎉

05/19/2024

So proud of Martin Mueller IV!

12/21/2022

Questions…..
How would you describe Achalasia in one short sentence?
How does your family help and support you?
What is the worse thing about Achalasia?
Let the world know and help our Achalasia with your answers.

07/15/2022

Let get involved in spreading awareness. We need some help in Atlanta on 6 August 2022. If you would like to meet another person with Achalasia and want to help with a booth for that day please message me or April Evans. Let’s make this happen.

06/21/2022

11/20/2021

The day is here. Tackling the Tour de Tucson all 102 miles of it. Merissa and I will be supporting the Achalasia Achalasia Foundation - Martin Mueller IV Achalasia Awareness Foundation and spreading the word of this rare disease. There are 6050 people in this ride this year. Go Achalasia family. You are not alone

11/07/2021

20 November 2021 is coming up fast. Show your support for Merissa’s and Martin’s ride in the Tour de Tucson on that day. We will have on the Achalasia Awareness bike jersey’s to help spread awareness of this rare disease.

09/06/2021

Saturday September 11: Come on out and see us at this event and meet the admins of the Achalasia Group. The foundation will have a booth set up and would love to have you join us and help spread awareness about achalasia while also supporting our veterans. This is going to be a fun event with music, games, prizes and raffles.

08/29/2021

Happening in two hours!!!

Join us on Sunday, August 29, 2021 at 3:00 p.m. on Zoom for a discussion about Achalasia. Please bring us your questions and we will do our best to give you answers! We would love to see you there!

To register:
- Go to www.achalasiainfo.com
- Scroll down on the main page until you see "Upcoming Events"
- Click RSVP!

**you will receive an email with instructions to join our meeting at the email that you provide in the registration**