09/16/2024
We need you!
π¨ Help Us Make a Change! π¨
We need your help sending a message of support for ICD-10 codes for Lipedema to the CDC!
π Before October 11, 2024, email [email protected] with this statement: "I support implementing ICD-10 codes for Lipedema now."
Tell whether you're a patient, provider or caregiver. You can then feel free to share your challenges as a patient or provider caused by not having diagnosis codes in place if you'd like. Please keep it short.
β Why is this a big deal? β
π With codes on every doctor's system, diagnosis can be tracked which means we will be able to know the true prevalence of lipedema soon.
πWith codes in place, doctors will have a consistent way to report that a person has lipedema.
πWith codes in place, the disease is legitimized. A medical provider cannot deny its existence if the codes are right there in the system.
πWith codes in place, it reduces the chaos that it is in the medical system for patients and providers. Diagnosis will surely come more quickly.
πResearch and grants will be easier to fund with a recognized separate code for lipedema.
πPatients can point to the codes when working with insurance for coverage of treatments, supplies, and surgeries related to managing their condition.
Getting ICD-10 codes in place now is foundational to all of the work we collectively (members of the ALA or not, right!) are trying to accomplish.
Please email the CDC at [email protected] with your support of ICD-10 codes for lipedema today. Thank you so much for your personal advocacy!