McLean Realty Group

06/01/2026

Honored to be a part of the inaugural class of the Alpha-1 Foundation Fred C. Walsh Speakers Bureau.

05/30/2026

Open House in Pacifica 1-5PM-come by and say hello!

04/25/2026

Doing an open house in my house! 12-4 @735 Montezuma Dr. in Pacifica.

02/26/2026

Here is the market report for San Francisco for the month of February!🏡

02/19/2026

This looks interesting!

Ahead of , NORD is going to Capitol Hill to highlight how patient advocacy drives innovation for the 30 million Americans living with rare diseases. You can join us!

Fewer than 5% of the 10,000+ known rare diseases have an FDA-approved treatment — but progress happens when patients, researchers, investors, and policymakers work together. We’re going to demonstrate how.

Join our Congressional briefing: “Patient Advocacy Driving Innovation for People Living with Rare Diseases”

📅 February 24, 2026
🕤 9:30–11:30 AM
📍 Capitol Visitor Center
🥪 Box lunch provided | Open to the public

Hear from leading voices in research, policy, investment, and patient advocacy:
• Pamela Gavin, CEO, National Organization for Rare Disorders
• Ada Hamosh, MD, MPH, FACMG, Johns Hopkins Medicine NORD Rare Disease Center of Excellence
• Rohini Kosoglu, Venture Partner, Fusion Fund
• Theresa Strong, PhD, The Foundation for Prader-Willi Research

Innovation starts with advocacy. We hope you’ll join us. RSVP here: https://bit.ly/4rRdaQa

02/18/2026

用英语说“新年快乐”
Gōng Xǐ Fā Cái
Happy New Year!

02/18/2026

With Alpha-1 Foundation – I just got recognized as one of their top fans! 🎉

02/05/2026

Follow me for more real estate advice 😂

02/05/2026

Thank you everyone who contributed to the KW blanket and sock drive! As a group we refilled our collection bin multiple times! They are in the process of being distributed! It is nice to make a difference for those who are living in the cold streets. Thank you again! ❤️

02/05/2026

Support rare diseases and if you know anyone with COPD from an unkown cause or a family history, please suggest they get tested for Alpha-1 Antitrypsin Deficiency.

Mark your calendars for on February 28th! This month, we’re lifting up the voices of the rare disease community to raise awareness, advocate for progress, and push for a future with earlier diagnoses and better access to care for people living with conditions like Alpha-1. To learn more, visit: https://alpha1.org/rare-disease-day/