Wonder why your stomach still sticks out even though you're hammering the core exercises every day? It's a common myth that bulging belly is due to weak abdominal muscles. Some people can look fat with a bulging stomach even if they're not fat. It's called Bulging Belly Syndrome.
I recommend that you incorporate these 10 Simple Moves into your day. They take less than 15-minutes to complete.
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IDF 2015 National Conference session, “Autoimmunity & Immunodeficiency – What’s the Relationship?” was presented by Kathleen Sullivan, MD, PhD on June 26, 2015.
A short video about climbing at the Castle Video Rating: / 5
In October 2015 The Castle Climbing Centre, one of London’s largest climbing centres, turned 20 years old. This short film documents it’s history from 1995 to the present day.
Your immune system is critical for fighting off disease, but millions of people around the world are immunocompromised. This means their immune systems have been weakened either by a genetic disorder or by chronic illnesses like AIDS, Cancer or Diabetes. Living with such diseases is hard enough at the best of times, but in the age of COVID-19 a positive test could be a death sentence.
As nations race to get their populations vaccinated those with an already compromised immune system are often not at the top of the list. How can overburdened medical systems keep these at risk people from falling behind?
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Recent data suggested that about 3% of Americans are immunocompromised, according to ABC News contributor Dr. Alok Patel.
Here you have it, the full, mostly unedited and uncut footage of me ascending the World’s Tallest Rock Wall in Reno, Nevada. This video skips all the nonsense associated with how I normally make videos. This is what I wanted when I was preparing to climb, so I took it upon myself to make it for anyone else like me.
The wall is roughly 164 feet tall and broken into 2 main faces, 70 feet and then 94 feet. The entire wall is mounted to the side of the Whitney Peak Hotel and gives some fantastic views of the surrounding downtown area that you might not normally get to see.
Fair warning, it’s also not for the feint of heart since you are literally clinging to the side of a building. Also, because it is outdoors, the ability to climb is weather permitting. I was lucky enough to be able to change my plans and climb the day before my reservation because there was a ‘storm’ blowing in.
If you feel up to the challenge too, you can find more info about pricing and signing up here:
Chronic Diarrhea | Approach to Causes, Secretory vs Osmotic vs Inflammatory, Watery vs Bloody Diarrhea
Chronic diarrhea is diarrhea occurring for greater than 2-4 weeks, and it is broadly categorized into secretory, osmotic, functional, inflammatory, and malabsorptive causes. Causes include medications, crohn’s disease and celiac disease among many others. Depending on the cause, we can see either watery diarrhea or bloody diarrhea, or diarrhea with or without food. In this lesson, we look at an approach to the cause of chronic diarrhea, including a variety of factors that can help determine the cause of chronic diarrhea.
I hope you find this lesson helpful. If you do, please like and subscribe for more lessons like this one!
JJ
**MEDICAL LEGAL DISCLAIMER**: JJ Medicine does not provide medical advice, and the information available on this channel does not offer a diagnosis or advice regarding treatment. Information presented in these lessons is for educational purposes ONLY, and information presented here is not to be used as an alternative to a healthcare professional’s diagnosis and treatment of any person/animal. Only a physician or other licensed healthcare professional are able to determine the requirement for medical assistance to be given to a patient. Please seek the advice of your physician or other licensed healthcare provider if you have any questions regarding a medical condition.
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Common Variable Immunodeficiency (CVID)
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Common variable immunodeficiency (CVID) is a primary immune deficiency disease characterized by low levels of protective antibodies and an increased risk of infections. Although the disease usually is diagnosed in adults, it also can occur in children. CVID also is known as hypogammaglobulinemia, adult-onset agammaglobulinemia, late-onset hypogammaglobulinemia, and acquired agammaglobulinemia.
NIAID supports research to determine genetic causes of CVID that may lead to therapeutic approaches to address the disease. Researchers also are exploring how antibody-based drugs may lessen the severity of the condition.
Causes
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CVID is caused by a variety of different genetic abnormalities that result in a defect in the capability of immune cells to produce normal amounts of all types of antibodies. Only a few of these defects have been identified, and the cause of most cases of CVID is unknown. Many people with CVID carry a DNA variation called a polymorphism in a gene known as TACI. However, while this genetic abnormality confers increased risk of developing CVID, it alone is not capable of causing CVID.
CVID is also linked to IgA deficiency, a related condition in which only the level of the antibody immunoglobulin A (IgA) is low, while levels of other antibody types are usually normal or near normal. IgA deficiency typically occurs alone, but in some cases it may precede the development of CVID or occur in family members of CVID patients.
Symptoms & Diagnosis
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People with CVID may experience frequent bacterial and viral infections of the upper airway, sinuses, and lungs. Acute lung infections can cause pneumonia, and long-term lung infections may cause a chronic form of bronchitis known as bronchiectasis, which is characterized by thickened airway walls colonized by bacteria.
People with CVID also may have diarrhea, problems absorbing food nutrients, reduced liver function, and impaired blood flow to the liver. Autoimmune problems that cause reduced levels of blood cells or platelets also may occur. People with CVID may develop an enlarged spleen and swollen glands or lymph nodes, as well as painful swollen joints in the knee, ankle, elbow, or wrist. In addition, people with CVID may have an increased risk of developing some cancers.
Doctors can diagnose CVID by weighing factors including infection history, digestive symptoms, lab tests showing very low immunoglobulin levels, and low antibody responses to immunization.
Treatment
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CVID is treated with intravenous immunoglobulin infusions or subcutaneous (under the skin) immunoglobulin injection to partially restore immunoglobulin levels. The immunoglobulin given by either method provides antibodies from the blood of healthy donors. The frequent bacterial infections experienced by people with CVID are treated with antibiotics. Other problems caused by CVID may require additional, tailored treatments.
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En este video les traemos una rutina de biceps y triceps (brazos) organizada en 3 bi series de biceps y 3 bi series de triceps. Asegurense de seguir las indicaciones exactamente como lo explica Emilio aqui para obtener los resultados ideales.
Climbing plants are perfect for brightening up bare walls and fences or hiding unsightly ones!
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PlantDo is here to give all of you home garden, landscaping, and home decor ideas. Here, you will find what you have been looking for.
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00:30 Clematis ☘️
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Rheumatoid arthritis is a chronic inflammatory disorder that can affect more than just your joints. In some people, the condition can damage a wide variety of body systems, including the skin, eyes, lungs, heart and blood vessels.
An autoimmune disorder, rheumatoid arthritis occurs when your immune system mistakenly attacks your own body’s tissues. Video Rating: / 5
This video “Primary Immunodeficiency” is part of the Lecturio course “Immunology” ► WATCH the complete course on http://lectur.io/primaryimmunodeficiency
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Severe combined immunodeficiency (SCID) is a group of rare disorders caused by mutations in different genes involved in the development and function of infection-fighting immune cells. Infants with SCID appear healthy at birth but are highly susceptible to severe infections.
Severe combined immunodeficiency – A deadly combination of defects of T & B lymphocytes + Natural killer cells
Its a primary immunodeficiency (inherited in the family) affecting T lymphoocytes, B lymphocytes and Natural killer cells in different combinations.
These children die within one year without a bone marrow transplantation.There have been cases like “David the bubble boy” who survived for 12 years in a sterile chamber isolated from pathogens.
Patients are small babies that suffers from fungal, bacterial, or viral infections since their immune system is not functioning as it should.
The symptoms can be:
recurrent infections resistant to antibiotics,
failure to thrive with abnormal growth curves,
diarrhea,
diaper rash,
bronchitis,
pneumonia,
otitis media,
liver abscess,
morbilliform rash,
oral candidiasis
Doctors can check the sequence of DNA to determine any mutations that would cause this disease.
One have to remember that the levels of antibodies decline after about 6 month of age if the baby fails to produce new ones for himself, since the antibodies from the mother are depleted.
So these babies may appear healthy for about 6 months.
Therefore we can check blood values of lymphocytes, natural killer cells and antibodies to easier determine which type of Severe combined immunodeficiency we are dealing with.
What are the types of this disease?
Mainly X linked recessive (IL2RG gene mutation at Xq13.1) and autosomal recessive .
The autosomal recessive have many types:
adenosine deaminase deficiency,
Jak3 intracellular kinase mutation,
Purine nucleoside phosphorylase mutation,
Omenn syndrome with RAG gene mutation,
Bare lymphocyte syndrome with MHC 2 gene mutation.
The adenosine deaminase deficiency cause an accumulation of dATP, which blocks the enzyme Ribonucleotide reductase (converts NDP to dNDP). Without dNDP there is no DNA synthesis and therefore no production of cells like T & B lymphocytes.
You can imagine that without T & B cells there is no real immunity against infections. We can see depleted zones in the hypoplastic lymphoid organs. One example being a small thymus lacking lymphocytes and Hassall’s corpuscles. On X-ray there is an abscence of thymic shadow.
The treatment?
Bone marrow transplantation and gene therapy. About 1 patient out of 5 have a risk of getting acute T cell leukemia when treated with bone marrow transplantation.
These videos are for informational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any Nordic Health Organization video. Video Rating: / 5
