So pleased for this lady, glad she is getting help, i hope all goes well for her. I am roughly the same shape and size of her, i cant afford surgery so i am doing treatments that are non surgical. Thank you for an informative video..
She has seen significant improvement after her compression and lipedema reduction surgeries . She has posted about her journey and changes on lipedema.net . Wishing you the best of health.
@@sarcasticcat4982 Wishing you the best of health. If you want to find out more, please go to www.lipedema.net/navigating-united-healthcare-insurance-for-lipedema-coverage.html or contact our office.
We dont know of any doctors in Michigan that work with lipedema patients. We do have patients from Michigan come to our office in St Louis for lipedema treatment.
How do I find a doctor that specializes in Lipedema patients in my area. I am 2 hours north of Los Angeles. I have pretty much self diagnosed. I have venous insufficiency now. My wrists and ankles are starting to cuff a bit. Kind of like this woman here.
The principal specialists who diagnose lipedema are Venous and Lymphatic Specialists and Vascular Medicine Specialists. However, some endocrinologists and primary care doctors are familiar with and can diagnose Lipedema. The key is to find a doctor who is familiar with Lipedema and comfortable making the diagnosis of Lipedema. We can recommend Dr Michael Schwartz and Dr David Amron in the LA area who treat lipedema surgically.
So pleased for this lady, glad she is getting help, i hope all goes well for her. I am roughly the same shape and size of her, i cant afford surgery so i am doing treatments that are non surgical. Thank you for an informative video..
She has seen significant improvement after her compression and lipedema reduction surgeries . She has posted about her journey and changes on lipedema.net . Wishing you the best of health.
Have you found a way for insurance companies to cover this yet?
We are getting good coverage from United Health Care comercial insurance .
@@lipedemainfo I will check into them! Thank you!
@@sarcasticcat4982 Wishing you the best of health. If you want to find out more, please go to www.lipedema.net/navigating-united-healthcare-insurance-for-lipedema-coverage.html or contact our office.
I am from Michigan, is there any known Dr. that work with Lipedema patients.
We dont know of any doctors in Michigan that work with lipedema patients. We do have patients from Michigan come to our office in St Louis for lipedema treatment.
So how do we fix it please
There are non surgical and surgical treatments for lipedema. You can learn more at www.lipedema.net/. Wishing you the best of health.
How do I find a doctor that specializes in Lipedema patients in my area. I am 2 hours north of Los Angeles. I have pretty much self diagnosed. I have venous insufficiency now. My wrists and ankles are starting to cuff a bit. Kind of like this woman here.
The principal specialists who diagnose lipedema are Venous and Lymphatic Specialists and Vascular Medicine Specialists. However, some endocrinologists and primary care doctors are familiar with and can diagnose Lipedema. The key is to find a doctor who is familiar with Lipedema and comfortable making the diagnosis of Lipedema. We can recommend Dr Michael Schwartz and Dr David Amron in the LA area who treat lipedema surgically.
Do you mind sharing the Dr. info?
@@angelicacervantes4563 is above in this thread in LA area. 😞
Dónde está ése médico
We are in St Louis, Missouri USA.