Moving to a new place can be nerve racking experience or a pleasant Furniture Removal Near Me in Rivonia one. It basically depends on how you choose it to be. Moving and packing go hand in hand and how you pack ultimately determines how your moving in experience to a new place finally concludes. You should focus on making things smoother rather than doing everything at the eleventh hour. Steps like getting together packing tools like padding, tapes, boxes, markers etc., cleaning the house for important items, and making reservations with the movers should be taken well before time. Similar steps which should be taken care of well in advance are discussed below –
Gather All the Goods and Items
Gather all the goods and items you need to pack in one place. It often happens that Small Furniture Movers important things are left behind and that is something you would not like when you are amidst unpacking in your new house/office.
Ready the Supplies and Boxes
Before you actually start packing your stuff, you need to make sure that you have all the pre-requisites such as boxes of different sizes, markers, duct tapes, and padding tools. It is very important that you have these in place before you start packing as it can be a real inconvenience getting these things later on.
Prepare Important Paperwork for the Move
Prepare a proper paperwork wherein you would have a detailed list of things that need to pack as well as the things that you have packed. It would come in very handy once you start unpacking.
Start Packing in Advance
It is always advised to start the packing process in advance. It not only saves you precious time but also reduces the hassles in the end. The lesser the hassles, Home Removalists the lesser the errors and mistakes. Even the best movers would advise you to do the same.
Use Proper Padding
Simply packing things is not enough. You need to make sure that you make proper provisions for the protection of the things you have packed. Proper padding is also important because you never know what is going to happen to your goods and how are they going to be treated. Sudden and uncertain accidents may damage your goods for good. It is thus, always advised to provide proper protection to your packed items. This can be done by bubble wraps or old and used clothes. You can even use Thermocol to add more protection to delicate items.
Take Pictures of Electronic Set-Ups
Electronic set ups can be hard to put back the same way as they were set up before. It often happens that people are unable to set up electronics the exact same way after they have moved into a new place. It is therefore highly recommended that you take photographs of such complicated electronic set ups so that you can late refer to these pictures while setting up again in your new house/office.
Pack in Separate Boxes
While packing your stuff, it is important that you use different boxes and that too of various sizes. It is imperative to do so as this will help you a lot while you unpack. Packers and movers would advise you the same as it is very convenient to unpack different things from different boxes as compared to unpacking everything from one single box.
Pack on An “Open – First” Basis
Last but definitely not the least, always pack your stuff as per ’Open – First” basis. While you pack, always put in stuff which you will need last. This way, when you start unpacking, you will get your hands on things that you need immediately.
Several Autoimmune DisordersDid you know there are more than 80 yypes of autoimmune disorders? No, I promise not to list all of them. I will briefly cover the more common autoimmune diseases that I haven’t written about in the past. I have recently written about Rheumatoid Arthritis, Sjogren’s Disease and several hubs on Lupus so you can read detailed information on those diseases. In the normal person, the body’s immune response protects them from invading diseases and infections. In a person with an autoimmune disorder things have gone haywire. Your body doesn’t recognize invaders from your healthy tissue, so your white blood cells or T cells attack healthy organs. They can virtually affect every part of your body. These diseases usually attack women, particularly African-American and Native-American women. Many autoimmune disorders have similar symptoms, which makes diagnosis that much more difficult. Often this process is frustrating as your first symptoms are fatigue, muscle aches and low fever. The diseases sometimes flare-up and sometimes go into remission. Most autoimmune diseases affect women more often than men, with higher percentages for Afro-Americans and Native-Americans people. Celiac DiseaseCeliac disease is another autoimmune disease characterized by an inappropriate immune response to dietary proteins found in wheat, rye, barley (gluten and gliadin). This response leads to inflammation of the small intestine and to damage and destruction of the villi that line the intestinal wall. These villi are projections (small folds) that increase the surface area of the intestine and allow nutrients, vitamins, minerals, fluids, and electrolytes to be absorbed into the body. When the villi are destroyed, the body is much less capable of absorbing food and begins to develop symptoms associated with malnutrition and malabsorption. When the body is exposed to the gluten and gliadin proteins, it forms antibodies that recognize and act against not only the grain proteins, but also against constituents of the intestinal villi. As long as the patient continues to be exposed to the proteins, he will continue to produce these auto-antibodies. Celiac disease is most prevalent in those of European descent, probably inherited, can affect anyone at any age. It is thought to be an inherited tendency that is triggered by an environmental, emotional, or physical event.. The possible symptoms include: abdominal pain and distension anemia bleeding tendency bloody stool bone and joint pain changes in dental enamel diarrhea fatigue greasy foul-smelling stools oral ulceration, weakness weight loss. Children with this disease may experience delayed growth and development. It is estimated that 1 in 133 people in the U. S. have celiac disease but only 3% have been diagnosed. Patients with celiac disease must follow a lifelong gluten-free diet.. Once all forms of wheat, rye, and barley have been removed from the diet the patient improves. It is important to detect and treat celiac disease as soon as possible, especially in young children. Celiac disease should be considered in infants who are not thriving, since foods with gluten are common and celiac auto-antibodies may begin to develop shortly after a child switches from milk to solid foods. In most cases the patient can lead a normal life by adhering to the diet. SclerodermaThis is in a group of rare, progressive diseases that involve hardening and tightening of the skin and connective tissues — the fibers that provide the framework and support for your body. Localized scleroderma affects only the skin. Systemic scleroderma also harms internal organs, such as the heart, lungs, kidneys and digestive tract. Scientists estimate that about 250 people per million have some form of scleroderma. The most prevalent signs of this disease include Raynaud’s phenomenon, Gastroesophageal reflux disease (GERD) which in addition to acid reflux you may have trouble absorbing nutrients, and skin changes which may include swollen fingers and hands, thickened patches of skin, particularly on the fingers; and tight skin around the hands, face or mouth. The skin will appear shiny because it is so tight. I have a friend with this disease and she must wear a restrictive binding on her left arm from the top to her wrist, which means she always wears long sleeves. That’s not much fun living in Florida. This disease affects not only your skin but also your blood vessels and internal organs; there are sub-categories defined by what area of the body is being attacked. One is called CREST and results from an overproduction and accumulation of collagen in body tissues. Native Americans get this disease 20 times more often than the general population, and it is more common with Afro-Americans as well. It occurs 4 times more often in women than men. While there is no known cause exposure to silica dust, common in coal mines and rock quarries, some industrial solvents such as paint thinners and certain chemotherapy drugs may exacerbate the disease. There is no cure and treatment is typically the same as that for lupus patients, corticosteroids, Plaquenil, and anti-inflammatory medications. PolymyositisThis is another uncommon connective tissue disease which is characterized by muscle inflammation and progressive weakness, particularly in skeletal muscles which control movement, involving those closest to the trunk of the body first. It most commonly occurs in 30-50 year old people. Signs usually develop gradually over weeks or months. The weakness is symmetrical; affecting both the left and right sides of your body, and tends to gradually worsen. Polymyositis is in a group of diseases or disorders of the muscles called inflammatory Periods of remission are possible. Treatment to strengthen muscles should start early as there is no cure. Other symptoms may include difficulty swallowing, speaking, mild joint or muscle tenderness, fatigue and shortness of breath. Treatment is corticosteroids, (which often start at very high doses then taper down), Cytoxan, cyclosporine and sometimes intravenous therapy of Immunoglobulin containing healthy antibodies from blood donors. There are several investigation drugs also being tried at the present time. These patients will need physical and speech therapy, plus a dietetic assessment. Raynaud’s DiseaseRaynaud's disease is a condition that causes some areas of your body — such as your fingers, toes, tip of your nose and your ears — to feel numb and cool in response to cold temperatures or stress. In Raynaud's disease, smaller arteries that supply blood to your skin narrow, limiting blood circulation to affected areas. It is more common in cold climates and also affects women more than men. This disease frequently is present along with other autoimmune diseases. During an attack of Raynaud's, affected areas of your skin usually turn white at first. Then, the affected areas often turn blue, feel cold and numb, and your sensory perception is dulled. As circulation improves, the affected areas may turn red, throb, tingle or swell. There are two type of Raynaud’s disease; primary and secondary. The secondary is considered the more serious disease and usually appear after 40 years of age. The causes of this disease are numerous; other autoimmune diseases, carpal tunnel syndrome, repetitive trauma, smoking, chemical exposure and certain medications including some blood pressure treatments Juvenile Rheumatoid ArthritisIts It is the most common type of arthritis of those under 16 years of age, affecting 50,000 in the U. S. It’s a chronic condition causing joint swelling, inflammation, pain, swelling, redness and stiffness. I t may also affect the eyes and internal organs. About 1/5th of patients have an enlarged spleen. There are 3 categories: Pauciarticular- about 50% of the cases are this type and most common in girls under 8 years old Polyartifular – about 30% of the cases and it affects 5 or more joints, especially in the hands and feet. Systemic – about 20% have this type and if affect both joints and internal organs. These children may have frequent fevers and rashes that come and go rapidly. Doctors diagnosis this disorder once a patient has had the symptoms for at least 6 weeks. These symptoms may include morning stiffness, limping, reluctance to move an affected joint, joint pain and swelling. Patients with systemic JRA may have intermittent fever, rash, swollen lymph nodes, and in some cases liver, spleen, (very rarely) lung involvement and eye inflammation. The cause of this autoimmune disease is also unknown. It tendency may be inherited but is believed to that a triggering event is required for it to emerge. Several types of blood tests and x-rays are done to aid diagnosis. There is no cure so treatment is to relieve the discomfort of the symptoms. It is a heart breaking disease to see children suffer. Autoimmune PancreatitisThe term "autoimmune pancreatitis" was first used in Japan in 1995 to describe a newly recognized form of chronic pancreatitis. Since then, Mayo Clinic has played a major role in identifying, describing and treating the disorder in the United States. Mayo Clinic researchers have identified 2 types of this disease including one that can develop as young as 12 years of age. It is diagnosed from several test with the most accurate being a core biopsy. Symptoms of autoimmune pancreatitis often improve dramatically after a short course of corticosteroids. But relapses are common, and some patients require additional or long-term therapy. Multiple Sclerosis This is a chronic autoimmune disease that affects the central nervous system. It causes Inflammation and the destruction of myelin. Myelin surrounds nerve fibers and acts like insulation on a wire preventing “short-circuits” that divert a nerve signal from having its desired effects. The “demyelination” process interferes with nerve impulse transmission, affects muscular control, and causes a variety of sensory, motor, and psychological symptoms. Again the cause is unknown but it is thought to be an autoimmune process triggered by a virus, environment factors and it has a genetic predisposition The first symptoms usually occur between ages 20-40. It affects women more frequently than men, is more common in Northern European Caucasians. It important to manage the symptoms of multiple sclerosis, as well as, treating the disease before permanent damage causes symptoms. Interferon, corticosteroids and several other medications are used. Wegener’s GranulomatosisThis is another uncommon autoimmune disease that affects about 1 in 20,000 people. Again there is no known cause or cure. Symptoms are due to inflammation that can affect many tissues in the body, including blood vessels (vasculitis), which makes it a very serious disease. It affects the upper (sinuses and nose), and lower (lungs), respiratory system and frequently involves the kidneys, lungs, eyes, ears, throat, skin and other body organs. Other symptoms include nasal membrane ulcerations and crusting, saddle-nose deformity, inflammation of the ear with hearing problems, inflammation of the eye with sight problems, cough (with or without the presence of blood), pleuritis, (inflammation of the lining of the lung), rash and/or skin sores, fever, lack of energy, weakness, fatigue, loss of appetite, weight loss, arthritic joint pain, night sweats, and blood in urine which may or may not be indicated by a change in urine color. Diagnosis is established by clinical and laboratory findings such as the ANCA blood test, other blood and urine tests, x-rays, and tissue biopsy. Treatment varies based on patient symptoms and disease activity. Corticosteroids and Cytoxan are the initial treatments, then Methotrexate or Azathioprine. Graves DiseaseGraves’ disease is the most common cause of overactive thyroid gland. It is caused by an auto-antibody that acts like thyroid-stimulating immunoglobulin which cause the thyroid to produce excessive hormones. It is usually seen in women over 20 and may cause symptoms and signs such as weight loss, increased appetite, hand tremors, heat sensitivity, sweating, nervousness, and in some patients, protruding eyes. Patients often have a higher heart rate and an enlarged thyroid (goiter).Radioactive iodine uptake in measured amounts is swallowed and considered a critical component for treatment. I had a friend with this disease and they finally "killed" her thyroid as she didn't respond to treatment. The symptoms made her miserable in the meantime. There Are So Many More DiseasesMy intent was to give you an overview of some of the better known autoimmune diseases. If you have one of the disease I'm sure you know a good deal more about it than what I wrote, but if you have symptoms maybe one of these descriptions will help you. Of course, you want to be seen by a doctor and remember your symptoms are real, not in your head as many of us were told before we got a diagnosis. Living with a chronic illness isn't easy but it is certainly better when you get it diagnosed and find out what you can do to improve your health. There is so much literature available on the internet, in books and I linked several hubs from other authors from Hub-pages that may be of help. I wish you all to be in the best of health!
Spleen Pain LocationSpleen pain can be perceived on the left side of the abdomen. The pain is generally perceived on the upper left side of the abdomen and somewhat felt near the back. The perception of pain on the upper left portion of the abdomen can also radiate towards the shoulder. The spleen is part of the lymphatic system and plays a part in the immune system while it is responsible for filtering and removing abnormal cells. The spleen is involved in so many functions of the body that it has a great risk for diseases and disorders. The approximate weight of the spleen in normal healthy adults is 200g with a size almost the same as the clenched fist. It is particularly located on the left side of the body just behind the stomach parallel to the 9th and 11th ribs and its structure is similar to the lymph node. The spleen is regarded as the largest organ of the lymphatic organ and contains two types of tissue known as the white pulp and the red pulp. The white pulp is the lymphatic tissue made up of white blood cells while the red pulp tissue is composed of venous sinuses and the "splenic cords". Numerous functions are being played by the spleen in the human body but humans can live without the spleen as many of its functions can be performed by other organs such as the liver and the bone marrow. The drawback in spleen removed from the body is the frequent episodes of infection one may suffer after it has been disengaged in the body. SymptomsIdentifying spleen pain is rather difficult during the early onset. There are signs and symptoms however that can help in determining a spleen pain and isolate it from other condition that may have similar symptoms with spleen pain. Symptoms are usually rare in spleen pain and the manifestation will only occur when the spleen has enlarged enough to cause signs and symptoms. The common signs and symptoms of spleen pain include the following: Pain perception on the upper left portion of the abdomen. The pain gets worse with every deep breathing. Pain radiates towards the back and shoulder. Abdominal tenderness Onset of high fever accompanied by spleen pain and may also be accompanied with chills. Frequent episodes of infection which can make an affected individual experience recurrent sickness. Occurrence of night sweats Loss of appetite and inability to eat a full meal Uneasiness or discomfort General body weakness and feeling of tiredness and restlessness. A symptom of low blood pressure and internal bleeding is a manifestation of ruptured spleen which requires an immediate medical attention as it is potentially life-threatening. Worsening abdominal pain with every deep breath also requires a prompt medical attention. The normal healthy spleen is usually not palpable during physical examination. Spleen pain in enlarged or swollen state can be easily palpated and felt by the attending physician or the examining physician. The onset of spleen pain should not be disregarded once noticed. It is beneficial to seek medical advice to prevent further medical complications and irreversible damage of the spleen. CausesThe involvement of spleen in various functions of the body made it potentially at risk for diseases and disorders. The soft and spongy characteristic of the spleen makes it potential for easy damage. A wide range of diseases and disorders can affect the spleen and its function while there are various causes of spleen pain such as: Splenomegaly This is the swelling of the spleen causing it to enlarge. The enlargement of the spleen will cause undue pain while it is potential for rupture when left untreated. It is necessary for an immediate medical intervention once the spleen ruptures as it is potentially life-threatening. The enlargement can affect the vital function of the spleen. As the spleen gets larger, it will both filter the normal red blood cells and damage the red blood cells as well. Mononucleosis Mononucleosis is a viral infection that can cause pain in the spleen. The infection is characterized by a swollen lymph node and onset of high fever. The level of mononuclear monocytes in the blood is marked with an elevation beyond the normal level. Endocarditis This is a bacterial infection of the inner lining of the heart or the endocardium. It is caused by a certain type of bacteria that infected other part of the body transmitted to the heart through the bloodstream contaminated with the bacteria. Toxoplasmosis Toxoplasmosis is an infection from a single celled parasite called Toxoplasma gondii. The single celled parasite is transmitted through an infected cat. Gaucher’s disease Gaucher’s disease is a rare hereditary disease that is characterized by accumulation of fatty molecules called cerebrosides. This hereditary disease can affect multiple organs of the body including the spleen. Felty syndrome Felty syndrome is a syndrome that is composed of three syndromes such as the enlargement of the spleen, rheumatoid arthritis and a very low count of the white blood cell. Some blood disorders can lead to the enlargement of the spleen which can give the spleen pain such as: Polycythemia Vera Polycythemia Vera is a chronic blood disorder characterized by a rapid overproduction of the bone marrow of both the white and the red blood cells including the platelets. Hemoglobinopathies Hemoglobinopathies is another blood disorder that can cause spleen pain. It is a genetic disorder of the blood that is marked by an occurrence of abnormal hemoglobin. Other causes of spleen pain include the following: A direct blow or injury to the spleen from any forms of physical trauma and accident Development of cyst or large pus adjacent the spleen Pressure on the lymphatic vessels that resulted from the blockage or clots TreatmentSpleen pain treatment is directed towards the cure of the underlying condition that is causing the pain. The mode of treatment depends on the underlying condition while the immediate action is pain relief to provide patient with comfort. Both pharmacological and surgical treatment is beneficial to spleen pain. Medications to reduce the inflammation and enlargement of the spleen may be prescribed. Spleen pain resulting from infections can be managed with antibiotics. Surgical removal of the spleen is also another option for patient suffering from spleen pain although post operation requires regular and careful monitoring as spleen removal will result to a frequent infection.
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