Are You Achalasia Aware?


Have you ever heard of Achalasia? Most of us can most likely answer this question with a simple no. More often than not unless we or someone else that we know is diagnosed with a disease, disorder and/or condition we are completely unaware that such a condition even exists. It is vital that we become aware and learn about such conditions so we can help in any way possible. One of the best ways to help is by first becoming aware and next by showing compassion for those who are afflicted.

Please take a moment to become Achalasia Aware by watching the featured video and also share the video to help spread awareness. For those who have been diagnosed with Achalasia, there is support, and you are not alone, so please click the Achalasia Support Map link that follows to join the Achalasia Support Map. has created an amazing platform for over 800 diseases, conditions and/or syndromes connecting them to others who can relate, so they can find connections and resources to help them through. Support is key for those who are diagnosed with such conditions and knowing that you are not alone gives great peace of mind.

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Health Support and Awareness Advocate with a lifelong dream of being an educator, Vanessa was well along the path towards realizing her goal, having completed an Associate of Arts in Natural Science, Associate of Science in Social Science, Bachelor of Arts in Liberal Studies, and her Master’s of Education, Adult Educators and Administrators. Close to the culmination of the education required to reach her goal of a teaching career geared towards K-12, Vanessa had to make a difficult decision. She asked herself, “Do I continue on with my dream of being a teacher or focus on saving mothers and babies by helping to discover a cause and cure for Hyperemesis Gravidarum?” Vanessa was a volunteering for the Hyperemesis Education and Research Foundation [HER] when she realized there were limited options available when fundraising as a volunteer. The Packs decided to create their own foundation, one that would support all organizations seeking to discover a cause and cure for HG. The Packs held the first ever HG walk on October 20, 2007, A Walk to Remember: HG Walk America, raising awareness in the community and gaining much-needed support for those suffering from the disorder. Proceeds of the walk were donated to the HER Foundation. During the completion of Vanessa’s Masters in 2012, the Ayden Rae Foundation was born. After the birth and survival of the Ayden Rae Foundation, Vanessa and her family grew to understand that there was a greater need for more awareness and support for all diseases/conditions/disorders/syndromes and together they plan to spread awareness about every disease/condition/disorder/syndrome they are made aware of and help connect those who suffer from those diseases; discover that they are not alone and find the resources available for them. It is vital that we all do our part to help eradicate all disease, so families are no longer suffering. It is noteworthy to point out that the worst disease on the planet that most in the world overlook is aging and death! Remember to always be willing to learn more about things you aren't aware of and show compassion for those who are afflicted; awareness and support is key for all of us ❤