Author Archive for: DaveDias

Shattered, Shaken and Stirred

Please checkout the sidebar where we have added information about Gil Ahren’s new book, Shattered, Shaken and Stirred.  We hope you will purchase their book.  My friend Gil and his bride, Kim, have been Shattered, Shaken and Stirred…and you will be too, when you read about the horrific journey they have been on.

A devastating car accident upends, disrupts and derails a seemingly ordinary family. In the wake of devastation is where recovery and, ultimately, redemption are found. Shattered, Shaken and Stirred explores and embraces the process of brokenness and healing in a way that is honest, heartfelt, and yet at times reassuringly humorous. Gil Ahrens offers his own journey not so much as a prescription for adversity, but as a comforting guidepost for how we might cope when confronted with life-altering challenges…when what we thought was safe and secure is suddenly taken away. He reveals how God s love and grace appear not necessarily when we want them, but certainly when we need them. This book is a real-life example of the power of reconnecting with what matters most. It offers hope and encouragement to anyone feeling the strain of life’s struggles.

Blessings to you and yours this Thanksgiving Holiday.
Dave

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All is In the Air!

All is In the Air!

Fall is in the air ….!!!

Our friends, Buford McCharen and his wife Victoria, had a parking lot sale this weekend in anticipation of moving to their new chiropractic office in Rio Del Mar.

Irene and Vic have a great time together ….!!!  These are the gracious people that afford Irene her toxin foot baths twice a week which supplements the kidney dialysis treatment.  Dr. McCharen also keeps her spine aligned ….!!!

We celebrated Jocelyn’s 29th birthday at Mobo’s Sushi Restaurant in Santa Cruz.  Jordan, Jocelyn’s boyfriend, joined us for the evening.

Having toooooooooo much fun ….!!!!!!  Quail Egg sushi rolls ….!!!

Jocelyn sporting her new coat and the hand made scarf that Irene finished knitting just a few days ago ….!!!

Wow, it’s hard to believe our eldest daughter is 29 years old …. which occurs technically on Thanksgiving Day this year, November 26th…!!!

We have MUCH to be thankful for ….!!!

Thanks for checking in, and for caring,

Dave

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Amyloidosis Description and Summary

This is a really good summary of Amyloidosis:

Definition
Amyloidosis is a progressive, incurable, metabolic disease characterized by abnormal deposits of protein in one or more organs or body systems.
Description
Amyloid proteins are manufactured by malfunctioning bone marrow. Amyloidosis, which occurs when accumulated amyloid deposits impair normal body function, can cause organ failure or death. It is a rare disease, occurring in about eight of every 1,000,000 people. It affects males and females equally and usually develops after the age of 40. At least 15 types of amyloidosis have been identified. Each one is associated with deposits of a different kind of protein.
Types of amyloidosis
The major forms of this disease are primary systemic, secondary, and familial or hereditary amyloidosis. There is also another form of amyloidosis associated with Alzheimer’s disease.
Primary systemic amyloidosis usually develops between the ages of 50 and 60. With about 2,000 new cases diagnosed annually, primary systemic amyloidosis is the most common form of this disease in the United States. Also known as light-chain-related amyloidosis, it may also occur in association with multiple myeloma (bone marrow cancer).
Secondary amyloidosis is a result of chronic infection or inflammatory disease. It is often associated with:
familial Mediterranean fever (a bacterial infection characterized by chills, weakness, headache, and recurring fever)
granulomatous ileitis (inflammation of the small intestine)
Hodgkin’s disease (cancer of the lymphatic system)
leprosy
osteomyelitits (bacterial infection of bone and bone marrow)
rheumatoid arthritis
Familial or hereditary amyloidosis is the only inherited form of the disease. It occurs in members of most ethnic groups, and each family has a distinctive pattern of symptoms and organ involvement. Hereditary amyloidosis is though to be autosomal dominant, which means that only one copy of the defective gene is necessary to cause the disease. A child of a parent with familial amyloidosis has a 50-50 chance of developing the disease.
Amyloidosis can involve any organ or system in the body. The heart, kidneys, gastrointestinal system, and nervous system are affected most often. Other common sites of amyloid accumulation include the brain, joints, liver, spleen, pancreas, respiratory system, and skin.
Causes and symptoms
The cause of amyloidosis is unknown. Most patients have gastrointestinal abnormalities, but other

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