@WolfofX I grew up not knowing my father. In 2023 I took a DNA test at the urging of my daughter. I found the surname I was looking for. My father had passed in 2003. I found 6 sisters and 1 brother. One sister had passed in 2020 and brother passed 3 mos. after I met him. I feel blessed.
@catturd2 My mother is blind, can no longer walk and has limited use of her hands. She wants to remain in her home but canโt afford caregivers because she makes too much money. People who work all their lives fall through the cracks and canโt get help but we give it away to illegals!
@dr_ericberg June is Lipedema awareness month. I wish for more people to know about it so if they know of a woman who suffers from this disease they can get some help. I would also wish the medical community to know about it as a lot of medical professionals have no idea what it is๐๐๐
@MattWalshBlog For me this is Lipedema awareness month. Myself and many other women have this disease and donโt know it. It was first diagnosed in 1940 and yet very few medical professionals know about it. My hope is to get peoples talking so hopefully we can get answers, help and a cure๐
@DrTurleyTalks For me this is Lipedema awareness month. Myself and many other women have this disease and donโt know it. It was first diagnosed in 1940 and yet very few medical professionals know about it. My hope is to get peoples talking so hopefully we can get answers, help and a cure๐
@michaeljknowles For me this is Lipedema awareness month. Myself and many other women have this disease and donโt know it. It was first diagnosed in 1940 and yet very few medical professionals know about it. My hope is to get peoples talking so hopefully we can get answers, help and a cure๐
@GuntherEagleman For me this is Lipedema awareness month. Myself and many other women have this disease and donโt know it. It was first diagnosed in 1940 and yet very few medical professionals know about it. My hope is to get peoples talking so hopefully we can get answers, help and a cure๐
@LarryDWilcox For me this is Lipedema awareness month. Myself and many other women have this disease and donโt know it. It was first diagnosed in 1940 and yet very few medical professionals know about it. My hope is to get peoples talking so hopefully we can get answers, help and a cure๐
@AntonioSabatoJr For me this is Lipedema awareness month. Myself and many other women have this disease and donโt know it. It was first diagnosed in 1940 and yet very few medical professionals know about it. My hope is to get peoples talking so hopefully we can get answers, help and a cure๐
๐๐๐June is Lipedema awareness month. Lipedema was first diagnosed in 1940 and most medical doctors and their staff have no idea what it is which can lead to a lifetime of issues for the sufferer. Hopefully, this will also help a woman you know who may have this disease!
@TaraBull808 I was actually considering it as I have Lipedema which is a painful disease. You cannot diet or exercise this fat away and I felt my only hope was Ozempic. My insurance wouldnโt approve it and I have since reconsidered. Not a lot is known about Lipedema so there isnโt much hope.
@KenDBerryMD I have Lipedema. I currently see no hope with this disease as there arenโt many in the medical community who even know about it. Iโm trying carnivore and have managed to loose some belly weight but have no hope for my legs or arms. Iโm just going to get more grotesque looking.
@VigilantFox@MidwesternDoc Such as with Lipedema which I have had since the onset of puberty. I didnโt know of such a disease, most doctors donโt either. Iโm in my 50โs and have been on blood pressure meds since my early 20โs! I will be talking to my new doctor(a vascular doctor)about this.
Lipedema is a disease that effects 11% of women with no cure, other than invasive and expensive liposuction. In my opinion there is no hope. Insurance companies donโt recognize Lipedema as a disease and consider liposuction cosmetic which leaves women to continue to suffer.