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Tryptasemia & Co-Morbidities

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When the Mountain's too Hard to Climb HATS

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities

20170815 132146Several years ago, our family had the good fortune to visit Quebec, Canada. I wanted to climb Mont-Saint-Hilaire, especially because of the pegmatite(s) found there. (See our Morefield mine project; that mine follows a pegmatite in Amelia, Virginia.) Our family walked together regularly, so this hike should not have been excessive.

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About Tryptasemia.com HATS

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities

tryptasemia logoTryptasemia.com and Tryptasemia.org were created to help people find information about Hereditary Alpha Tryptasemia Syndrome quickly.

Read more: About Tryptasemia.com HATS

Tryptasemia: a Quick Primer HATS

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities

tryptasemia logo

Hereditary Alpha Tryptasemia, or HAT, has also been called familial tryptasemia and hypertryptasemia. Here are a few important numbers to remember (updated 3/2023).

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Confirming whether You Have HATS

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities

tryptasemia logoMany people with Hereditary Alpha Tryptasemia Syndrome, or HATS, have struggled through years of doctors, specialists, tests, and medications already. Determining whether one has multiple copies of the TPSAB1 gene has become easier since 2018.

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Faces of Tryptasemia HATS

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities

Xander 2014

If you have recently discovered you have Hereditary Alpha Tryptasemia Syndrome, you're not alone. We're gradually adding faces and stories.

Read more: Faces of Tryptasemia HATS

Twenty Minutes (with Tryptasemia) HATS

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities
  • mastcell
  • music
  • cough
  • performance
  • hymns
  • Giardini
  • piano
  • itching
  • pain
  • maneuver
  • heal
  • healing
  • cell
  • mast
  • hereditary
  • alpha
  • tryptasemia
  • syndrome

post it piano

This is the original published version of this story. An abridged version was published on Mast Cell Research as a winner in their October 2017 story contest. In March 2018, I was diagnosed genetically with Hereditary Alpha Tryptasemia Syndrome.

 

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Apology Accepted

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Written by: Karen Smith-Will
Parent Category: Research
Category: Tryptasemia & Co-Morbidities

Photo of waspThis article was written in 2010, 8 years before I was confirmed genetically to have Hereditary Alplha Tryptasemia Syndrome. It was written as a business article, but it details the challenges I experienced before understanding the nature of my illness and how it impacted daily life.

Read more: Apology Accepted

Subcategories

HATS Stories Article Count:  4

 

 

Every rose has its thorn

When the mountains too hard to climb

20 minutes (with Tryptasemia)

Apology accepted

Thirst

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