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Pasquale Ferretti’s Story

Twenty-five years ago, an unwelcome visitor barged in on me.  This visitor became an obnoxious pest that made my life miserable.  I experienced literal headaches as a result.  I soon discovered that the intruder proved to be a thief.  My peace of mind, independence, and health were stolen.

Why wouldn’t I boot this interloper out?  The answer lies in the fact that it was not possible.  You see, the unwelcome “guest” goes by the name, scleroderma. It is a disease that cannot be erased.

Scleroderma took many things from me.  It also brought me a number of things:  pain, stiffness, numbness, choking episodes, and other unpleasant effects.  It proved to be a relentless force that wore me down mentally and physically.  I naturally became discouraged and frustrated by its onslaught.  I was powerless!

In early 1981, Dr. Paul Wenig, D.O. entered the equation.  He was new to Botsford hospital.  In fact, I was his very first patient there.  After he examined and tested me, Dr. Wenig confirmed my diagnosis.  He stated that while scleroderma was no picnic, there were things I could do to help the situation.  He suggested I join a support group and utilize available resources.  He gave me hope by telling me that the disease affects various people in different ways…it wasn’t necessarily a death sentence.

Visits to support groups and physical therapy helped me restore confidence.  In addition, conversations with family, friends, and clergy led me to relax.  Now stress became less of a factor.  This process took several months to get rolling.

I soon developed a routine that brought positive results.  I suggest that scleroderma patients establish a plan of action as soon as possible.

  1. Talk to your loved ones.
  2. Meet others with the disease.
  3. Exercise (even though difficult at times)
  4. Rest…listen to your body.
  5. Never quit, giving up is not an option!
  6. Visit physicians regularly.  New treatments can help control problems.

Realize that coping with a catastrophic illness is a facet of life that some of us must face.  A quarter century of experience in resisting scleroderma makes me an expert.  I view myself as a survivor, not a victim.  Sometimes I forget I even have scleroderma.  I work hard.  Life is still good!

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