Journal Pioneer

Spreading the word

Anne White feels ‘really motivated’ to raise awareness about her rare condition

- BY JIM DAY

Anne White does not bemoan being among the extremely few P.E.I. residents living with the rare disease called acromegaly.

She is upbeat, in fact.

The 68-year-old Three Rivers woman was diagnosed in 2015 with this rare hormonal disorder caused by a benign tumor of the pituitary gland in adults.

She has likely had the condition much longer, but the disease often goes undiagnose­d. While three to four in one million persons per year are diagnosed with acromegaly, it is actually present in 60 out of one million persons.

White says just over a handful of Islanders are currently diagnosed with the disease.

Acromegaly can be difficult to diagnose because of its slow progressio­n and varied symptoms, which include abnormal growth, swelling of the hands, feet and facial features, increased spacing of teeth, deepening of the voice, headaches and problems with vision.

White has several of the symptoms. Her feet have grown from size six to size eight. Her hands have also grown much larger.

Her voice has deepened considerab­ly from a previous soprano voice for the profession­al musician who once taught music in school and still leads choirs.

She also believes carpal tunnel syndrome and arthritis in her right hip can be attributed to acromegaly.

Still, she is fairing very well compared to many others with the disease.

She remains active, walking and swimming on a regular basis.

Her pain is manageable.

And her spirit is high.

“I consider myself very fortunate,’’ she says. “Some people with acromegaly suffer terrible headaches and terrible pain and discomfort in their joints and various places.’’

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