Keratoconus is a progressive condition and can be a debilitating if left untreated. Watching your family members go through it can make you feel helpless and useless in some experiences. You probably have many questions on the condition after watching your family members go through their treatments. In past years their were limited treatments for Keratoconus and eventual cornea transplants were needed for the patient to keep their quality of vision. This type of treatment had a long recovery period and often caused the patient pain.
Today’s treatments have improved a lot since then and quite honestly there is little to no pain with many of them. Patients have much shorter recovery times, and have a much better quality of vision without replacing their corneas. Still many people have questions when they find out a family member is going through a condition like Keratoconus. The condition can often cause a reduced activity level and sometimes have complications in their normal lives. A few questions maybe “Will I get Keratoconus?” or “Will they go blind?”.
While these are all reasonable questions, and having a family member with Keratoconus is one of the highest risk factors of Keratoconus it doesn’t guarantee that you will get it. It only tells you to watch yourself and your eye health a little more. Getting annual eye exams can help with early detection. Taking care of your eyes can help lessen your chances of developing these conditions later on down the road.
Below are some tips to reduce your chances of developing Keratoconus:
Avoid rubbing your eyes
Get annual eye exams
See an eye care professional that specializes in Keratoconus
Protect your eyes regularly
Reduce stress in your life
Below are Signs of Keratoconus:
Frequent Eye Rubbing
Frequent Changes in prescriptions
Blurred or double vision
Halos or glares around lights
Sensitivity to light
Poor night vision
Squinting or Straining Your Eyes
There are probably many more questions you want to ask. Finding an eye care professional that specializes in Keratoconus is always best. Looking for one that deals with Keratoconus patients daily would be best.
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