My new book Jeans on a Beach Day is Here! Written just for YOU!

Jeans on a Beach Day: a book for the beautiful woman hiding her legs.

FOR IMMEDIATE RELEASE

Jeans on a Beach Day: A book for the beautiful woman hiding her legs
Susan O’Hara, with foreword by Brenda Viola

Imprint: Independently Published by Kindle Direct Publishing
Availability: https://amzn.to/3JPOkdd


On sale: April 21, 2022
Price: $8.99
Pages: 107
ISBN: 9798443835211

CONTACT
Susan
legslikemine@gmail.com

Yukon, OK, USA.  Jeans on a Beach Day: A book for women who are lipedema patients, or who have symptoms of lipedema, including unusually large legs, hips, or arms, nodules, and fat deposits that may not make sense, and are exploring the possibility that they may have the painful fat disease. The book provides numerous resources, personal patient stories, and quotes that will help the reader understand that she is not alone, and is part of a community of 11% of women in the world with lipedema who need to seek treatment soon to avoid progression. The book is available on Amazon.com for $8.99 and includes QR codes for easy linking to important resource sites and information for medical professionals who may not have been exposed to lipedema during their medical training, but wish to gain information to help their patients with lipedema symptoms.

ABOUT THE AUTHOR
Susan O’Hara is from Yukon, Oklahoma, and is the founder of LegsLikeMine, LLC. Susan has suffered from lipedema for more than two decades, starting with the birth of her first child in 2001. Her condition progressed slowly through various hormonal changes, but flared to a new level with a significantly stressful work-related event that served as the catalyst for seeking surgical treatments.

Like many, Susan went undiagnosed for almost 20 years, suffering pain and slowly losing mobility. Despite diet, exercise, and having two weight-loss surgeries, the condition persisted. After numerous MRIs, knee surgeries, x-rays, and a bout with tendonitis, a technician asked Susan who was treating her LYMPHEDEMA, and this got her connected to support groups, who actually saw her pictures and suggested she had LIPEDEMA.

Susan’s informal, online diagnosis allowed her to begin research, finding specialists and therapists familiar with lipedema, who were able to clinically diagnose and provide treatment. Through her research she discovered compression wraps and massage techniques to help manage her condition. In 2021, Susan had three Lymph-Sparing Lipectomy surgeries, and incorporated a regular swimming routine into her life to help manage lipedema.

Susan has struggled for years to find boots, shoes and clothes that fit and help highlight features other than her legs. She has dedicated a portion of her social media presence to help others with the condition continue to find and showcase their own beauty and belonging by sharing her fun ideas in fashion in her own, fun, way.

LegsLikeMine is a work of passion and necessity in hopes that it will get information to women who badly need help and who may not know they have the painful fat condition called lipedema.

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LegsLikeMine supports the 11% of the women in the world, who have lipedema.

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