The Cookbooks

Family and friends are jumping in to help. They put together this wonderful cookbook to sell to help with the cost of Jared's liver transplant. They gathered 650 recipes and typed each one up. Sent them off for printing and we ended up with beautiful cookbook full of fabulous recipes from all our family and friends. Special thanks goes to those that helped type in recipes and proofread each one...twice. Also, there is much gratitude to those who submitted recipes and who are in full swing selling cookbooks so fast we will likely be sending for a second shipment soon, and the first one arrived only a day ago. You all know who you are. THANK YOU!

Cookbooks are $14 each + $3 shipping if you live outside of the Salt Lake City, Utah area.
Please contact Paulette if you would like to order a book, paulemay@msn.com Thank You!

Miles away????

Time for an update. So Jared had his apt. with the hepatologist yesterday. And we left feeling quite discouraged. The Dr. said he thinks the pains Jared has been having are his gallbladder and is doing some tests and looking at removing it now if it needs to be. He went over his chart and asked a bunch of lame questions...seriously, LOL. To sum it up he told us Jared is miles away from Transplant...."miles" what the heck does that mean?? The appt. took 2 1/2 hours and what we took from it was it is going to be a long time before they even consider listing him, and he scheduled our next clinic appt. for next May. I was annoyed and we were both a little upset when we left. Well I decided I wanted more answers so I called the transplant coordinator this morning. Long story short. Jared's MELD score jumped from a 10 last August to a 14 as of yesterday. They will list him at a 15. She said with a 14 they recheck the MELD every three months unless he gets really sick, then we can call them and they will check it. Patients usually get the transplant when the MELD reaches somewhere in the 20's. She is going to speak with the Dr. and let me know what the game plan is. So anyway I feel a little better now and I am not thinking it is going to be years away. On another note I am happy to tell everyone the cookbooks have been completed and shipped and should be here by Monday or Tuesday of next week YAY

Waiting

I don't like waiting. It's been about two months now, since we found out Jared needs a liver transplant. He has a "supposedly" rare genetic disorder called Alpha 1 Antitrypsin deficiency. He has the ZZ phenotype and it is destroyed his liver. I guess they call it rare because of the people that have this ZZ phenotype 95% of them have lung problems not liver. Anyway He has to get dental clearance before they will move ahead with putting him on the transplant list. He has 2 dentist appointments left, then we can move along. Well move along to more waiting......

Alpha-1 Antitrypsin Deficiency

Alpha 1 and a liver transplant

Jared is a 34 year old husband and father of four children. He comes from a family of ten siblings. Family is everything to him. Jared has been sick off and on for the last few years. He got really sick in February of 2010 while visiting family in Colorado. He went to the urgent care there and they did numerous tests and CT scans and found his liver and spleen to be much enlarged. The doctors told him and his wife that he may have Lymphoma. After returning home they saw his regular doctor and they did more blood work and CT scans and came to the conclusion that he had a virus called CMV. He seemed to be better after about a month. About the same time the following year he began having the same symptoms again. He went back to the doctor where more tests were given. Tests for the same virus came back negative so he was sent for more blood tests and CT scans. His liver and spleen were again much enlarged and they were told again that Lymphoma was a possibility. Jared was referred to a gastroenterologist who ordered more blood work and a Liver biopsy. Before the results came back the doctor stumbled onto something and immediately sent Jared for more blood tests and a chest x-ray. He found that Jared has a rare genetic disorder called Alpha 1 Antitrypsin deficiency (ZZ gene) and stage four cirrhosis of the liver. The only cure for Alpha 1 and liver disease is a liver transplant. After learning about the disease they had their family tested for it. Two of Jared’s sisters have the same disorder with the ZZ gene but are not showing any signs of liver or lung disease yet. Two of Jared’s children have the SZ genes, which puts them at risk for lung disease. Right now it is just an awareness issue with the children and they are taking precautions to avoid harmful substances that are harmful to the lungs. Right now the main focus is getting Jared a liver transplant. The cost for a liver transplant is about $500,000. While the family does have health insurance it will still be quite a financial burden, we anticipate the out of pocket costs to be approximately 20,000 the year he receives the transplant. The cost of the surgery is only the beginning. Prescription medications following the surgery are $120 per month after insurance pays. There are several medications Jared will have to take for the rest of his life so his body doesn’t reject the new liver. These medications will surpass the family’s annual deductible within the first few months each year.

Alpha 1 (ZZ) leads to emphysema in 95% of people with the disorder, only 5% get liver disease. Alpha 1 is often misdiagnosed for 7 years or more. Many people that have the disorder and have no idea it even exists. Awareness is the key, and a simple blood test is all it takes.

What is Alpha-1?

Alpha-1 Antitrypsin Deficiency (Alpha-1) is a condition that is passed from parents to their children through their genes. This condition may result in serious lung and/or liver disease at various ages in life. For each trait a person inherits, there are usually two genes and one gene comes from each parent. People with Alpha-1 have received two defective alpha-1 antitrypsin genes. One defective gene came from their mother and one from their father. There are many types of defective alpha-1 antitrypsin genes. The most common abnormal genes are called S and Z. Normal genes are called M. A person who does not have Alpha-1 will have two M genes (MM). People identified with Alpha-1 most commonly have two Z genes (ZZ). Current evidence suggests that there are about 100,000 people with Alpha-1 (ZZ) in the United States. Another deficient gene combination is SZ, although people with this gene combination are less likely to get lung or liver problems than those with two Z genes.

Alpha-1 occurs when there is a lack of a protein in the blood called alpha-1 antitrypsin or AAT that is produced by the liver. The main function of AAT is to protect the lungs from inflammation caused by infection and inhaled irritants such as tobacco smoke. The low level of AAT in the blood occurs because the AAT is abnormal and cannot be released from the liver at the normal rate. This leads to a buildup of abnormal AAT in the liver that can cause liver disease and a decrease of AAT in the blood that can lead to lung disease.

Governor, Gary Herbert of Utah has graciously proclaimed November 2011 as Alpha-1 Awareness Month. This is the 2nd year the Governor has issued a proclamation for the Alpha-1 Community