University of california san francisco | about ucsf | ucsf benioff children's hospital search site | find a doctor conditions & treatments conditions & treatmentsa-z medical dictionary medical tests patient education patient experiences special programs doctors doctors & staff directory find a doctor expert q&a and profiles clinics all clinics & centers outreach clinics find a clinic clinical trials search clinical trials research ucsf latest research getting care appointments acute care or emergency? cheap no prescription viagra International services maps & directions mychart parking ucsf & hill physicians additional support bookstore newsletter archive patient services support groups your hospital stay admissions and discharge hospital policies patient rooms patient safety billing & records billing health insurance medical records notary getting to ucsf medical center maps & directions parking visiting patients accommodations food services visiting hours & guidelines send a patient a message gift shops patient referrals & transfers make a referral labor and delivery transport transfer a patient request a consultation additional resources careers at ucsf medical center continuing education newsletter archive nursing program ucsf medical group our organization annual reports executive biographies hipaa & patient rights ucsf partners in care quality of patient care mission bay join our team career information nursing program news & press ucsf in the news newsletter archive press releases ways to give how to donate volunteering print this page email this page font size home > conditions & treatments > blood diseases > amyloidosis conditions & treatments conditions & treatmentsa-z medical dictionary medical tests patient education special programs amyloidosis amyloidosis is a group of diseases in which abnormal proteins, called amyloid proteins, accumulate in organs or organ systems such as the heart, kidneys, nervous system or gastrointestinal tract. There are different types of amyloidosis, dependent on the type of protein being deposited in tissues. The most common form of amyloidosis in the united states is called primary amyloid. In primary amyloid, the protein being deposited is a part of the antibody protein called the light chain. Primary amyloid is now a treatable disease. The mainstays of therapy are the same agents used to treat a related bone marrow cancer, called multiple myeloma. Treatment options include chemotherapy, corticosteroid medicines, biologic agents, and in some instances, autologous stem cell transplantation. generic viagra fast shipping The goal of therapy is to halt the buildup of amyloid protein in organs and to prolong life. cheap viagra tablets Fortunately, amyloidosis is rare, affecting about eight out of every 1 million people annually. overnight viagra The majority of those affected are more than 40 years of age and 60 percent are male, although the condition can affect anyone. The cause is unknown. cheap viagra next day delivery Show more types of amyloidosis there are three main types of amyloidosis: primary amyloid — this is a plasma cell disorder originating in the bone marrow. cheap viagra Abnormal cells produce antibody proteins which deposit as amyloid. It is the most common type of amyloidosis in the united states, affecting 2,000 people each year. This condition, which is usually treated with chemotherapy, is not considered to be a type of cancer. However, it may be associated with multiple myeloma, which is a type of bone cancer. cheap viagra tablets The severity of the illness often depends on the number and extent of organ involvement. Secondary amyloid — this condition is caused by a chronic infection or inflammatory disease such as rheumatoid arthritis, familial mediterranean fever (an intestinal disorder), osteomyelitis (infection of bone) or inflammatory disorders of the bowel. buy discount viagra The amyloid deposits in this type of the disease are made up of a protein called the aa protein. Medical or surgical treatment of the underlying chronic infection or inflammatory disease can slow or stop the progression of this type of amyloid. Familial (or hereditary) amyloid — this rare form of amyloid is the only type that is inherited. It affects families of nearly every ethnic background. The deposits in this type are most commonly made up of the transthyretin protein produced in the liver. The condition results from a mutation in this protein. cheap viagra online Liver transplant is used to cure this form of amyloid. Show less signs and symptoms diagnosis treatment symptoms of amyloidosis depend on the organs it affects. discount viagra The wide range of symptoms often makes amyloidosis difficult to diagnose. Some people may not experience any symptoms and others may have many symptoms. Frequently described symptoms include: weakness weight loss shortness of breath numbness or tingling in the hands or feet diarrhea severe fatigue an enlarged tongue feeling full after eating smaller amounts of food than usual dizziness upon standing swelling of the ankles or legs fainting spells palpitations of the heart show more a complete medical history and physical examination is essential for diagnosing amyloidosis. Blood, urine and bone marrow tests also must be performed. Blood or urine tests can detect the amyloid proteins, but only bone marrow tests or other small samples of tissue — called biopsies — can positively establish the diagnosis of amyloidosis. A small tissue sample, or biopsy, will often be taken from the abdominal fat, rectum, and/or bone marrow to confirm the diagnosis of amyloidosis. generic viagra cost These biopsies are relatively minor procedures done in an outpatient clinic with a local anesthetic (numbing medication). Occasionally, samples need to be taken from damaged organs such as the liver, intestines, heart or kidney. The type of biopsy procedure required will vary from patient to patient. Treatment of amyloidosis is given to improve symptoms and extend life. cheap viagra tablets Treatment can limit further production of amyloid pr.
 
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