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Hypokalemic Periodic Paralysis, Gitelman's Syndrome, Andersen Tawil Syndrome and Bartter's Syndrome are a group of rare genetic disorders affecting more than 14,000 men, women and children in North America alone.
People with this disorder have a dramatic and urgent need to test their potssium level frequently.
Many cannot work because of their disorder and to make matters worse did not discover their disorder until they had children. Today there are families suffering from the same genetic disorder. The hardship and daily struggle is unimaginable to those of us without the disorder. Go to Facebook and look at the following groups for an idea as to how important what we are trying to achieve really is.
Gitelman's Syndrome,
Andersen Tawil Syndrome,
Parents Of Periodic Paralysis Kids,
Fighting Bartter's Syndrome,
Amigos del Sindrome de Bartter-Gitelman,
Periodic Paralysis International,
Periodic Paralysis Association
Go to Statpathtech.com to read about what it's like to live with on of these rare genetic disorders on a daily basis.
These pages represent a fraction of the people all over the world suffering because their potassium levels do not adjust correctly.
At Statpath Technologies, we are 6 months and $100,000US away from making our dream a reality.
We are 6 months and $100,000US away from helping thousands and thousands of families get back their lives.
The donated money will be used immediately to begin the final stage of converting our current system to digital so that the analyzer will be compatible with smartphones.
We need your donations now.
We need $10 or $20 per person or as much as you can afford.
As soon as we get to $75,000US we can start the conversion.
Please review the links above and google Hypokalemic Periodic Paralysis etc. to understand how much of a difference your donation will make to the people afflicted with these terrible genetic disorders.
You can get more info at statpathtech.com.
People with this disorder have a dramatic and urgent need to test their potssium level frequently.
Many cannot work because of their disorder and to make matters worse did not discover their disorder until they had children. Today there are families suffering from the same genetic disorder. The hardship and daily struggle is unimaginable to those of us without the disorder. Go to Facebook and look at the following groups for an idea as to how important what we are trying to achieve really is.
Gitelman's Syndrome,
Andersen Tawil Syndrome,
Parents Of Periodic Paralysis Kids,
Fighting Bartter's Syndrome,
Amigos del Sindrome de Bartter-Gitelman,
Periodic Paralysis International,
Periodic Paralysis Association
Go to Statpathtech.com to read about what it's like to live with on of these rare genetic disorders on a daily basis.
These pages represent a fraction of the people all over the world suffering because their potassium levels do not adjust correctly.
At Statpath Technologies, we are 6 months and $100,000US away from making our dream a reality.
We are 6 months and $100,000US away from helping thousands and thousands of families get back their lives.
The donated money will be used immediately to begin the final stage of converting our current system to digital so that the analyzer will be compatible with smartphones.
We need your donations now.
We need $10 or $20 per person or as much as you can afford.
As soon as we get to $75,000US we can start the conversion.
Please review the links above and google Hypokalemic Periodic Paralysis etc. to understand how much of a difference your donation will make to the people afflicted with these terrible genetic disorders.
You can get more info at statpathtech.com.
Organizer
Richard Krelstein
Organizer
Beverly Hills, CA