In a small town in Brazil, a remarkable pair of identical twins, Elis and Eloá, have become an inspiring symbol of resilience and the extraordinary power of the human spirit. Born with Hutchinson-Gilford Progeria Syndrome, a rare and fatal genetic condition that accelerates aging, these twins are navigating their challenging journey with a grace and strength that has captured the hearts of many around the world.
HGPS is an exceptionally rare disorder, affecting approximately 1 in 20 million newborns worldwide. Characterized by rapid aging beginning in early childhood, children with progeria typically exhibit growth delays, loss of body fat and hair, aged-looking skin, stiffness of joints, and severe cardiovascular disease. The average life expectancy for those with HGPS is around 14.5 years, though some may live into their late teens or early twenties. This syndrome became popular with the movie The Curious Case of Benjamin Button.
The condition is caused by a mutation in the LMNA gene, which produces the lamin A protein responsible for maintaining the structural integrity of the cell nucleus. The mutation results in the production of an abnormal version of the protein, called progerin, which causes cells to become unstable and die prematurely.
Their family members EXPLOIT them on MANY social media platforms (as many as 5 different videos posted in a day). In many videos, it's evident that their special needs are not being met. The $$ that is profited from all the EXPLOITATION is spent by family members for expensive new phones, designer clothes, eating out at Restaurants, large screen TVs and other grossly extravagant items. The girls could be on the latest medication that helps extend their life expectancy and ease the pains associated with the syndrome. However, profits are not spent on any of this. The families have distorted views of their priorities. Their daily activities are focused on creating content for videos, to post on social media. There are numerous videos that show one toddler being hit by the other, with adult hands forcing this. The girls deserve better!
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Elis and Eloá quickly drew attention due to their unique medical condition. Despite the physical challenges posed by progeria, their infectious smiles and unwavering optimism have become a source of hope and inspiration. The twins' parents, Guilherme and Elismar, have devoted their lives to providing the best care possible for their daughters, ensuring that they live as normal a life as possible despite the constraints of their condition.
The family's journey has not been easy. Daily life involves rigorous routines of medical care, including physiotherapy, to manage joint stiffness and maintain mobility. Yet, Elis and Eloá face each day with remarkable courage and a zest for life that is truly extraordinary.
Elis and Eloá's story has resonated with people around the globe. This led to a groundswell of support from individuals and organizations dedicated to raising awareness about progeria and supporting research efforts. The Progeria Research Foundation, a key organization in this field, has been instrumental in advancing research and providing resources for families affected by the condition.
Through social media platforms, the twins' journey is shared with a broad audience, fostering a sense of community and solidarity. Their family's updates, documenting both the highs and lows of their daily lives, provide invaluable insights into the realities of living with progeria, while also spreading a message of hope and perseverance.
Significant steps have been made in understanding and treating progeria in recent years. In 2020, the U.S. Food and Drug Administration (FDA) approved the first treatment for progeria, a drug called lonafarnib. This medication has been shown to extend the lives of children with progeria by reducing the buildup of progerin in cells, thus slowing down the progression of the disease.
While there is still no cure, ongoing research holds promise. Scientists are exploring gene editing techniques, such as CRISPR, as potential avenues for correcting the genetic mutation at the source. For families like that of Elis and Eloá, these advancements offer a glimmer of hope for the future.
Elis and Eloá exemplify the extraordinary resilience of the human spirit. Their story reminds us all of the power of love, community, and scientific advancement in the face of seemingly invincible challenges. As they continue to defy the odds, they inspire countless individuals around the world to cherish every moment and never lose hope, no matter how daunting the obstacles may seem.
She uses them as a $$ maker! Videos are posted multiple times a day on many accounts on each social media platform. The twins deserve better than this!
The caregivers are being spotlighted on many of the social media platforms for the EXTENSIVE exploitation of the girls. EXPLOITING children with physical deformities for profits is a CRIME.
I watch Eloa and Elise daily, and I agree that sometimes I feel their needs are not being met, but at other times they are being fully met. I'm also torn when I sense one is receiving more attention than the other, or is vying for attention but does not receive it, and wondered if they didn't have the syndrome,whether I would be so emotionally attached to their actions and reactions. I am not sure why I'm so addicted to watching them.. I tend not to watch the videos where I sense their impediment is being exploited, in favour of more natural and organic videos involving them. I have grown to love them, and although I cannot tell how old they are, I love how beautiful they are, although one appears to be a little aggressive and spiteful, but sibling rivalry is in many families. Thanks for sharing them with the world.
