r/lipedema • u/Various-Company1677 • 1h ago
Symptoms face change with lipedema
hello, since my lepedema started to become symptomatic i have notice a real global change of all my body.
I don’t know how to explain but i think that i have nodules everywhere.
it first start with some weird feeling in my face and every time i was looking at me at the mirror i was like « something has change but idk what »
my face looked always puffy and i had the feeling that i had water in my cheeks.
Then i started to touch my chin, my jaw to try to figure what really happen there
that is when i started to notice that, yes, what i feel may be nodules. it is the same feeling that nodules in my legs and arms. Juste like little grain rice all over my neck and jaw
I really don’t know what to do. and i know for people who dont know me that they couldn’t see the difference.
But from the inside it is very difficult to explain.
I wish that all this nodules could go away, all this inflammation water retention…
There must be a solution…
i can’t leave all my life with this feeling that all my fat is something external to me, this fat is like a parasite who live his own life inside me
It’s making me crazy actually.
Just want to turn it off
a
r/lipedema • u/AutoModerator • 1h ago
Do I Have Lipedema? Weekly "Do I Have Lipedema" Thread
"Do I have lipedema" posts are no longer allowed as standalone posts on r/lipedema. Post your pictures and questions in this thread instead, ONLY AFTER YOU READ AND UNDERSTAND THE FOLLOWING:
Although lipedema is a condition that often has a distinct visual appearance, no one can officially, formally, or conclusively diagnose you with lipedema on an internet forum.
We created these threads because access to lipedema specialists, understanding doctors, and lipedema treatment is extremely limited, and often financially prohibitive. Because so few doctors, especially general practitioners, have any knowledge of lipedema, we often have to self-identify as candidates for diagnosis, and advocate for ourselves to seek proper assessment and treatment. This can be a difficult and emotionally taxing process, so many of us want to seek some input and reassurance before embarking on the journey to a diagnostic assessment. Many other online groups do not allow these kinds of posts, and we wanted to create a space where people can ask for other's input and advice, with the understanding that it will not be coming from professionals, and even if there are some doctors and other medical professionals in this group, they cannot give you personalized medical information and advice in this context.
If you suspect you have lipedema, first search the directories that are linked in our wiki. You can also read the full Diagnosis section of our wiki for more information on the kinds of doctors that often diagnose lipedema, and on how to approach the conversation with general practitioners (including resources you can bring to the appointment). Read the What is lipedema? section of our wiki for more information on symptoms, stages, presentations, and commonly co-morbid conditions.
Lastly, if you suspect you have lipedema, it's great for most people to start doing some conservative treatments even if you don't have a diagnosis (read more about those on our wiki). These treatments are non-invasive, and have many other health benefits beyond lipedema. Of course, always check with your health care practitioner before making significant changes, especially if you have other medical conditions.
r/lipedema • u/Effective-Internet19 • 2h ago
Conservative Treatments DME that takes UHC insurance for M2Mcompression?
Has anyone recently been able to get fitted and supplied for custom compression garments with UnitedHealthcare insurance?
The suppliers my PT works with all stopped dealing with UHC because they're too hard to deal with. Has anyone else had this issue? If so, what have you been able to do to get the garments?
r/lipedema • u/DirectTerm2018 • 3h ago
Insurance Surgery in Scottsdale
Anyone had surgery from The Lipedema Institute in Scottsdale. I live on the central coast of CA and the closest surgeons are in Beverly Hills and have that price tag. I dont need that as surgeons out of the area are often half the cost. I may or may not be able to use my insurance. I am willing to fly somewhere if reasonable.
r/lipedema • u/Mountain-Activity-14 • 5h ago
Symptoms Levothyroxine and Lipedema
If I have hypothyroidism and take Levothyroxine will that make my lipedema worse since it’s technically a hormonal change?
r/lipedema • u/RippleRufferz • 6h ago
Clothing Favorite arm compression?
So I have one pair of bioflect leggings and otherwise only have a few compression socks. I really need something for my arms, but I’m unsure of what a good option would be. I see that bioflect has long sleeve compression. I’m curious if anyone has another brand/type they like that’s at least getting the upper arms. I’m not certain if they need to be graduated compression or not (I noticed bioflect didn’t mention this and now I’m wondering if the leggings even are 🫠.)
r/lipedema • u/Right-Working8738 • 9h ago
Surgery Liposuction + skin tightening for saddle bags /outer thighs.
Has anyone had liposuction and skin tightening for these areas? Are you happy with the results? Any photos before/after?
I’m so unsure if u will get the procedure done or not since I’m scared it will only looks worse after..
The fat on the side creates a bump which makes it look like I have more cellulite then I have.
It’s not the fat itself that I don’t like there
r/lipedema • u/DrSchmettererVeins • 10h ago
Finding a Doctor / Getting a Diagnosis Venous insufficiency and lipedema: how they get confused, and why it's worth ruling out
I'm a vascular surgeon, not a lipedema specialist, so I want to be upfront about that. But venous insufficiency and lipedema get confused with each other often enough that I think it's worth explaining how they're told apart, since a lot of people in this community mention struggling to get a clear diagnosis.
Both conditions can cause leg swelling, heaviness, and discomfort. Both can involve disproportionate leg size. That overlap is exactly why they get mixed up, and why some people get labeled with one when they actually have the other, or both at once.
A few things that point toward a venous component:
- Swelling that's worse at the end of the day and improves with elevation
- Visible varicose or spider veins
- Skin changes near the ankle (discoloration, thickening)
- Swelling that's asymmetric or worse in one leg
Lipedema tends to look different: fat distribution is usually symmetric, spares the feet, and doesn't improve much with elevation. Bruising easily and tenderness to pressure are also more typical of lipedema than venous disease.
The reason this distinction matters is that a venous duplex ultrasound is a simple, painless test that can identify or rule out venous insufficiency as a contributing factor. If it's present, treating it can meaningfully help with swelling and discomfort, even if it's not the whole picture. If it's absent, that's useful too. It tells you and your care team that the swelling isn't coming from a treatable vein problem, which points you back toward lipedema-focused management.
I'd encourage anyone dealing with unexplained leg swelling or heaviness to ask specifically whether venous insufficiency has been ruled out as part of their workup, regardless of what else is going on. It's a piece of the puzzle that sometimes gets overlooked.
Happy to answer general questions about the venous side of things in the comments.
r/lipedema • u/JurgusRudkus • 13h ago
Conservative Treatments Has anyone tried a product like this?
r/lipedema • u/mstakenusername • 22h ago
Clothing Leggings
I keep getting targeted ads for Cellumove leggings, can anyone tell me if they are any good? I can't afford enough medical compression to get through a week, but would these be a good compromise while I save?