Q & A with Sharon's son, George Episode 152 Special Guest Laura Olmos
An interview with Laura Olmos, Life doesn’t have to be perfect to be wonderful https://www.togetherforsharon.com/laura-olmos-life-doesnt-have-to-be-perfect-to-be-wonderful/
Laura Olmos (Mexico):
She was diagnosed with Parkinson's in 2013, at the age of 40, although the symptoms appeared a decade earlier. She founded Parkinson Laredo as a Facebook group during COVID pandemic and after that as an in-person support group too, on both sides of the border (Nuevo Laredo in México and Laredo, Texas in the United States).
Her commitment extends to participation in local, national, and international events related to Parkinson's, awareness. She has learned the importance of a healthy lifestyle, which includes specific care, regular exercise, and a balanced diet, among other aspects, to live fully despite Parkinson's. As an Ambassador of the Davis Phinney Foundation, she is enthusiastically dedicated to spreading this valuable message.
She promotes art as a form of expressing what a person feels living with Parkinson’s.
She has participated with her paintings in Parkinson’s Art exhibitions and auctions in London, and more recently with TheQuiver.org in Austin, Texas.
For this next World Parkinson’s Congress in May 2026 (Phoenix, Arizona) she has been invited to collaborate in the Fundraising Committee as well as in the Parkinson’s Advocate Committee.
Laura celebrates life as it is, sometimes adapting activities and enjoying time with family and friends. Loves practicing yoga, painting, traveling, and outdoor activities.
https://davisphinneyfoundation.org/ambassador/laura-olmos/
https://www.instagram.com/worldpdcongress/p/C_wLd0AySgu/
https://www.youtube.com/shorts/EvI7Uoa0p_c
https://www.instagram.com/parkinsons.art/p/Cf-8v3ioi_A/?hl=am-et&img_index=1
Laura Olmos
The togetherforsharon Podcast
World Parkinson Congress
Davis Phinney Foundation
TheQuiver.org
Parkinson Laredo
Karl Ste
Q & A with Sharon's son, George Ep 151 Special Guest
Jeanne Quinn SHAKE AND FREEZE®️
OUR VERY FIRST HOLIDAY SHOW!
An interview with Jeanne Quinn from the SHAKE AND FREEZE®️ Parkinson’s Campaign https://www.togetherforsharon.com/jeanne-quinn-from-the-shake-and-freeze/
The SHAKE AND FREEZE®️ Parkinson’s Disease Campaign is an awareness and fundraising campaign. We incorporate costumes, giveaways, humor, music and the spirit of the Christmas/Winter Season to get attention to our cause. Our big day “SHAKE AND FREEZE”®️ Day (AKA “Shorts Day’) is a recognized published special day where we wear shorts and other festive attire on the Winter Solstice, the “short” test day of the year. Dec. 21 is also Dr. James Parkinson’s death anniversary!
ShakeandFreeze.com
https://shakeandfreeze.com/
https://www.instagram.com/ShakeandFreeze
https://www.michaeljfox.org/sites/default/files/media/document/MVP20-p-s.pdf
https://www.instagram.com/togetherforsharon/p/CxzDjfCsofg/
The togetherforsharon Podcast
The Michael J. Fox Foundation for Parkinson's Research
Shake and Freeze
Team Fox
Holiday show
Holiday show time! Behind the scenes of Q & A with Sharon's son, GeorgeThis Parkinson’s community means the world to me and inspires me to keep fighting until we find a cure! Never stop fighting and I will be right by your side! https://www.togetherforsharon.com/qa-with-sharons-son-george/ The togetherforsharon Podcast The Michael J. Fox Foundation for Parkinson's Research Team Fox Shake and Freeze
Be a part of the future to share awareness for PD throughout the world.
Q & A with Sharon's son, George
Please visit, share and support us as we share for Parkinson's awareness and hope for a cure!
https://www.togetherforsharon.com/qa-with-sharons-son-george/
where I interview those inside and outside of the Parkinson’s community for awareness throughout the world and to help end Parkinson’s disease. The more awareness… the closer we maybe to a cure.
�If you have someone you are interested in me interviewing, please message me or any tips, topics, and questions you may be curious about, let me know and I will research them all. Sharon’s son, George
#togetherforsharon #parkinsonsawareness #endparkinsonsdisease #findacure #thetogetherforsharonpodcast
The togetherforsharon Podcast
Thank you
Thank you Mr. Fox! The Michael J. Fox Foundation for Parkinson's Research Team Fox
The Michael J. Fox Foundation for Parkinson's Research
The togetherforsharon Podcast
Team Fox
Shake and Freeze