Diagnosis Lipedema - How to Find an Expert

Specialized healthcare professionals are usually required to confirm the diagnosis of lipedema. Coordinating appointments with different healthcare professionals, finding compression garments that are comfortable and fit well - all together, it can be overwhelming. But managing your condition is easier with the right professional support at your side. In this article, we want to offer some guidance on finding experts to support your treatment after your diagnosis has been made.

Diagnosis Lipedema - How to Find an Expert

Find the Right Dealer for Compression Garments

It is not yet entirely understood how compression therapy improves the signs and symptoms of lipedema. However, compression therapy is believed to have an anti-inflammatory effect on fatty tissue, improve blood circulation, and reduce oxidative stress. Therefore, consistently wearing your garments can improve pain which is linked to inflammation and reduced oxygen supply of your affected limbs

Finding the right dealer to get garments that are comfortable to wear is therefore essential. For made-to-measure garments, several measurements at various points on the affected limbs are needed. Depending on your anatomical shape, specific adaptations might be required to ensure that the garments fit perfectly. As soon as you have found your first compression garments, you can use the JOBST Garment Reminder Service to receive a note when it’s time to get a new compression garment.

Find the Right Professional Support

Treating lipedema requires experts from different specialties who must work together. We already talked about the importance of qualified personnel at the medical supply store. Additionally, a dietician or nutritionist can support your weight management. Regular exercise and movement therapy, supported by a physiotherapist can contribute to maintaining a healthy weight and to feel better about yourself. You might also seek psychological support to learn strategies for coping with a long-term condition. Lipedema is still considered a rare disease, and many healthcare professionals have little knowledge of it. LymphCare provides a Therapist finder function to help you find the professional support you need.

Find the Right Community

Sharing your thoughts and struggles with your family and friends, as well as joining a community of like-minded people, are essential steps in coping with your situation. So many people out there have already made this journey. They can share their experience, knowledge, and strategies for managing lipedema. That’s why platforms like LymphCare are great options for connecting with others, whether you’ve just received your diagnosis or if you’re already a lipedema expert yourself.

Get Support From Others With Your Condition

It’s important to know you’re not alone. Join our private community and feel empowered by connecting with other lymphedema or lipedema patients.

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Don’t sit around and go through this in silence. Share your story. Doing that was a real eye-opener for me

Claudia Lymphedema patient