General Discussions

I am a board member of the United Multiple Sulfatase Disease (MSD) Foundation. Every year the organization sponsors a Zebra run in Ocean Springs, Mississippi to raise awareness and support for the organization. Alexandria Chilimidos, a second year Stanford GC students is organizing a pop up run in Northern California. We would like to organize one in SoCal also! Please contact either me or Alexia if you would like to help. This is great opportunity to support the rare disease community! Please contact us at: adchili@stanford.edu or michellefoxgc@gmail.com

Hello all, I am thinking of becoming an LLC for both private practice and applying for contract positions. Is anyone willing to chat with me about their experience doing this? I am debating between hiring a company to help me or doing it myself, etc.

Thanks in advance!

Michele

Wanted to let the SCGC community know about PKDfree.org offering financial assistance to patients and families with PKD seeking PGT-M and IVF who do not have insurance coverage.

Hello! I have been asked by a family to provide a referral for hereditary cancer GC and possible testing. They prefer a large University / Medical Center for GC and possible testing. Multiple family members with breast cancer, prostate cancer, and ALL. Any suggestion of which facility would be best? OK to send reply by text (951) 217-6641 or email mlourdessapriza@gmail.com. Thank YOU! Maria Sapriza-Ryan, MS, LCGC