Why aren't patients getting genetic testing? We want to hear from you!

Provider won't order? Can't get a specialist appointment? Genetic counseling appointment delays? Lack of insurance coverage?

DM us what issues you've faced in accessing genetic testing. We want to find new ways to help.

Getting answers shouldn't be expensive or complicated. Our simple at-home kit tests for 4,000+ rare diseases - completely free for individuals who qualify.

If you or a loved one are dealing with unexplained symptoms you may qualify for free testing.

Visit: probablygenetic.com

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD) is a rare autoimmune condition in which the body mistakenly attacks myelin, causing inflammation in the brain, spinal cord, and optic nerves.

If you think you have MOGAD or do have MOGAD - shoot us a DM.

#MOGAD

Chaz Lucius - a first-round NHL draft pick - made the decision to retire from hockey after being diagnosed with Ehlers-Danlos syndrome. His story is a powerful reminder of the impact rare genetic conditions can have and the importance of getting diagnosed.
#ChazLucius #DiagnosisMatters #RareButReal

Let’s talk about something important: genetic testing for kids with an autism diagnosis.
1. Autism is often the first diagnosis rare disease families receive
2. Rare diseases can hide behind other labels
3. Early diagnosis = better care & more support
Apply for free testing: chat.probablygenetic.com

Rare disease book club: Fourth Wing 📚

The novel features Violet Sorrengail, a character depicted with Ehlers-Danlos Syndrome (EDS).

Representation matters. Join us in celebrating stories highlighting the strength of those living with rare conditions.

On average, patients living with a rare disease wait 5-7 years for an accurate diagnosis, see up to 8 physicians, and experience 2 to 3 misdiagnoses.

If you are navigating the diagnostic odyssey and need genetic testing, apply for our free WES program: chat.probablygenetic.com

WHIM syndrome, an acronym for Warts, Hypogammaglobulinemia, Infections, and Myelokathexis, is a rare primary immunodeficiency disorder characterized by a compromised immune system, leading to increased susceptibility to infections and other health complications.

Read more: bit.ly/41rFAoo

FTD is a form of dementia that can cause memory loss, behavior changes, speech difficulties, and other symptoms. Age of onset can range from 45-65.

If you or a loved one has been diagnosed with FTD, apply for free genetic testing at chat.probablygenetic.com.

Genetic testing is a powerful tool in identifying rare disease patients and providing answers to a range of symptoms and sometimes multiple misdiagnoses. But the test itself isn’t enough to provide answers – that’s where a genetic counselor is needed.

Read how GCs fill the gap: bit.ly/4jt9z7N

It's #rarediseaseweek.

Did you know 72% of rare diseases are genetic? Yet, genetic testing is often overlooked, delayed, or not recommended for patients with unexplained symptoms. At Probably Genetic, we aim to educate, raise awareness, and improve access to genetic testing.

Over 400 million people worldwide are affected by rare diseases, and many remain undiagnosed. At Probably Genetic, we're committed to changing that through no-cost genetic testing and personalized guidance. Learn more at www.probablygenetic.com

#GeneticTesting #PatientAdvocacy #ProbablyGenetic

Probably Genetic offers free genetic testing to help individuals pinpoint the root cause of their symptoms while connecting them with vital resources, such as genetic counselors and advocacy groups.

Read the entire blog post and learn about our free genetic testing programs here: bit.ly/41qGEK