Huntington’s Disease Causes Chorea Muscle Contraction Symptoms of Huntingtons Disease

Huntington’s disease is an incurable, progressive disease that causes brain nerve cell wasting. As a result, you will likely experience chorea symptoms, which is an irregular and uncontrolled muscle contraction disorder.

Rarely does Huntingtons chorea and this disease’s other symptoms present before middle age. Its earliest symptoms often involve emotional changes, such as

  • anger
  • irritability
  • depression
  • mood swings
  • decision making difficulties
  • inability to answer questions
  • learning new information problems
  • not remembering important information

Those around you may notice these differences before you do. Your initial physical symptoms of Huntington’s disease may cause:

  • grimacing
  • clumsiness
  • trouble driving
  • balance problems
  • involuntary facial movements

These symptoms can be a signal for other diseases. Therefore, an accurate diagnosis from you health care professional is strongly advised.

As the disease progresses, you may develop these other Huntington’s disease symptoms:

  • bruxism
  • dementia
  • eating difficulties
  • loose walking ability
  • swallowing complications
  • inability to shift your gaze
  • severe balance, coordination issues
  • speech may become hesitant, halting, slurred
  • chorea ~ sudden unorganized muscle contractions

Huntington’s disease typically causes these degenerative symptoms to develop slowly. And which of these symptoms you actually develop is unique.

Huntingtons chorea will eventually cause your death, but it typically doesn’t happen for at least 10 years after your original symptoms.

If you develop Huntington’s disease at an early age, your symptoms will typically mimics Parkinson’s disease, and you might endure seizures.

Two unfortunate truths about Hungtingtons disease is that if you have its defective gene you will eventually develop the muscle contracting symptoms of this disease and your children have a 50% chance of being born with this incurable disease as well. Science is on the cholesterol accumulation hunt to change this foreseeable outcome.

As for now, gene testing is available to determine if you have it. If you don’t you will neither develop Huntington’s nor pass it on.

After your onset of Huntington’s disease, symptoms continue until your passing. The actual cause of death is generally a result of disease complications, like an infection or a fall.

The current state of treatment includes medication and therapy to help manage some of Huntington’s symptoms. But they won’t slow your progression nor stop your muscle contraction “dance” causing disease.

If you are in the throws of this health impinging disease, don’t give up. Here are a couple of suggestions to assist with some of Huntington’s disease contracting muscle challenges:

  • exercise regularly
  • use cups with lids
  • maintain adequate nutrition
  • wear sturdy, stable footwear
  • bendable straws for drinking
  • cut your food into small pieces
  • eat puree food for ease of swallowing
  • drink plenty of fluids to avoid dehydration
  • limit dairy products ~ causes choking mucus
  • keep your environment sharp, hard object free

It’s not out of the ordinary for your body to burn in excess of 5,000 calories, in part due to your involuntary muscle contractions. So you’ll need to consume more calories to maintain your health.