F̲I̲B̲R̲O̲A̲U̲R̲A̲T̲U̲S̲ ̲ ̲-̲ ̲ ̲ ̲ ̲"̲G̲o̲l̲d̲e̲n̲ ̲S̲t̲a̲t̲u̲e̲ ̲D̲i̲s̲e̲a̲s̲e̲"̲
⠀⠀▮⠀The gradual and eventually ossification of one's connective tissues, muscles, and organs. Often originating in the ligaments or tendons patients, few studies have shown it grow upon vital organs. The genetic condition ultimately immobilises and shuts down functioning tissue, covering it with a second layer of bone -- usually golden or yellow in colour.
The condition is a defect that appears before the age of 10 years old, often diagnosed around 7 years. It is a genetic defect, a mutation, of the ACVR1 gene. It is life long and debilitating.
S͟Y͟M͟P͟T͟O͟M͟S͟
• continuous bone growth
• chronic pain
• numbness or "heaviness"
• unsteady, disregular heartbeat
• Hypotension (Low blood pressure)
• difficulty moving
• brain fog
Often patients also report a lack of hunger, extra weight, slowed movements, and chronic migraines.
There is no known cure for fibroauratus, pain management and micro surgeries to remove and replace the solidified, damaged tissues are usually arranged to help treat and postpone the growth. It still, despite best efforts, remains inevitably a fatal disease.
In few cases Fibroauratus has been studied and noted to appear in organs that were weakened, or held underlying chronic health conditions beforehand. Typical cases find it appears in the liver, pancreas, or larger intestines first. Rarer studies show Fibroauratus appear in heart and lungs simultaneously.
The disease ultimately drastically decreases one's lifespan. But whilst a debilitating disease, the treatments for it can help one live a relatively normal life before progression reaches beyond treatment. Bio-mechnical skin is engineered to adapt and layer as a temporary patch, replacing the localised area of damage for up to ten years before needing to be replaced.