Prevention of Fat Loss and Lipoatrophy of the Face
A Video Blog
October 3, 2011
(Dr Albert Canas applies Sculptra in my face)
Yes, many people are very afraid to start their HIV medications because of lipoatrophy or lipodistrophy (fat loss or gaining fat in some areas). Well there are many options now. One of the most important parts of a person's body is their face. This is like the cover of a magazine, and how we represent ourselves! Many people feel very depressed because they lose fat in their face and become stigmatized by it! Although medication is better today as it was 20 years ago, I use Sculptra to prevent fat loss in my face. I see the pain in peoples' eyes when they suffer from this. It makes them very depressed and makes them want to hide! Once they get their face back, I see them thriving, working, loving everything.
It's just very sad that sometimes, as Dr. Canas mentions in my vlog, that the most adherent patient is the one that can suffer from this condition the most! It is not fair! We should look how we feel in the inside ... not have high Tcells and undetectable viral loads, but with a face that is nothing like the person they use to see in the pictures! I am not talking about aging gracefully ... I am talking about holes in your cheeks and looking like a skeleton! So I am thankful that there is new and better medication out there with less side effects, as well as there are fillers like Sculptra, that either give you your whole life back or like me ... PREVENT IT FROM HAPPENING AS LONG AS I CAN!
As always love and light,
Maria T Mejia
(The following video blog is in a 6-part series)
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Time to Show My Face and Take the Stigma Away
Maria T. Mejia
I am a Colombian female who lives in Miami, Florida. I've been positive for 20 years. Although almost all my life I've been in long-term relationships with HIV-negative men, I am happily married to a woman who is wonderful and caring. We have been together almost three years and she is HIV negative. I have no children but we will look into having! I am an activist, a peer educator, a caregiver. I volunteered for the Red Cross in education for the Hispanic HIV community and also the American community. I was a pre- and post-test counselor. I have spoken in many conferences and done a lot of outreach in the community, especially in the schools for prevention and education. It is part of my everyday life to educate everyone I can on this subject. Being HIV positive is nothing to be ashamed about! We are strong women, and we will take away all the stigmas slowly but we have to open up.
Read more blogs by women living with HIV/AIDS at "A Girl Like Me"
The Well Project shares its content with TheBody.com to ensure all people have access to the highest quality treatment information available. The Well Project receives no advertising revenue from TheBody.com or the advertisers on this site. No advertiser on this site has any editorial input into The Well Project's content.
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August 25, 2017 - My Response to Someone Who Denies Undetectable = Untransmittable: A Blog Entry by Maria T. Mejia
25 de agosto de 2017 - Mi Respuesta a una Persona que Niega a Indetectable = Intransmisible
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July 10, 2017 - Health Is a Human Right and I Am Not a Carrier! A Blog Entry by Maria T. Mejia
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