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A child’s understanding of Juvenile Arthritis

Arthritis is a wide spread problem throughout the world, with many people experiencing some form of the disease. With over 200 forms of arthritis officially recognized, it is important to know all that you can about the disease.

Three types of chronic arthritis affect children:

Pauciarticular Arthritis:   Affects about half of all children with Juvenile Rheumatoid Arthritis (JRA,) affecting mostly girls and especially girls under age eight who are most likely to develop this type of JRA.

Pauciarticular disease is a disease of few joints. It most commonly affects the knees, elbows, wrists, and ankles. The joints are usually affected asymmetrically (one joint on one side). Children affected by Pauciarticular disease usually have a positive antinuclear antibody (ANA) test and are prone to an inflammatory eye condition, iridocyclitis. Children with Pauciarticular JRA generally do well.

Polyartiucular Arthritis:   Polyarticular arthritis is a form of rheumatoid arthritis that causes pain and swelling in five or more joints. It can strike adults and children. Normally, Polyarticular arthritis affects larger joints like the knees, however it can also impair small joints in the hand, feet, jaw and neck.

Systemic Juvenile Arthritis:

The systemic form affects 20 percent of all children with juvenile rheumatoid arthritis. A small percentage of children develop arthritis in many of the smaller joints, which produce symptoms of general illness and can have severe arthritis that continues into adulthood.

The cause the arthritis is unknown; however, it is believed the disorder may be inherited. The inflammation of the joints can also be the result of a tick, which can cause Lyme disease. It is therefore important for you to be seen by your doctor and have the symptoms checked.

Juvenile Rheumatoid Arthritis.

If you have been diagnosed with JRA, you will have swelling in your joints. Many people get different forms of arthritis but having it when you are a child can be a little complicated, but most children do out grow JRA.

Symptoms:

  • The following symptoms may appear for several weeks or months.
  • Body temperature above 39◦C. or 102◦F.
  • Swollen glands over the whole body.
  • A blotchy non-itchy rash.

Treatments:

If any of the above symptoms are present, a doctor should be consulted within twenty-four hours from the time they first appeared.

You may find that your joints will start to hurt. Sometimes you will feel fine, other times the pain is very sharp and hurts a lot.  This is called a “flare-up” at these times you will find that the pain will keep you awake at night.   When you wake-up in the morning on these days you will find that soaking in a warm bath for a while will before you start you day will help, the pain a little and eases the swelling around the joints.

Although you cannot join in some of the activities other children participate in there are special exercises that are important in taking care of your arthritis.

To find out what is best for you, regular visits to physiotherapy are very important:

  • Weight training, helps your leg muscles to stay straight and in the right position.
  • Some children use braces or splints on their legs, hands and feet at night to keep them straight or prevent deformity in the joints or just to rest them during the day.
  • Swimming is another good way to exercise, as the water helps work your muscles without straining them.

Medications: 

Doctors may prescribe something to ease the discomfort and pain.

  • Aspirin, Non-steroidal anti-inflammatory drugs, (NSAID) such as ibuprofen to relieve pain and swelling.
  • If these drugs are not effective, drugs that are more potent may be prescribed such as corticosteroids.
  • At time some of these medications taste terrible, I always have a candy after mine.

Some of the steroid medications help with the pain a lot, but unfortunately they do have side effects, it can make your face all puffy, and take the calcium out of the bones making them soft.  In these cases, a diet high in calcium will help a lot.

Operation:

In severe cases, an operation may be performed to replace joints that are painful and damaged or to lengthen muscles that are causing a deformity.

Outlook:

As mentioned above most children do grow out of arthritis completely, one third will continue to have symptoms for many years.  In the remaining cases, the condition will get worse.

One other important thing note is that your eyes should be examined on a regular basis, for signs of Iritis, which is the inflammation of the iris and the muscular ring that surrounds it. Serious attacks are rare in childhood, but some children with JRA may suffer from a persistent or recurrent form of Iritis.

Over the years there have been many studies made and programs setup so as to give both children and adults some relieve, and as long as you listen to your body, you can be enjoy the things like other people, just doing them in a way so as not to put stress on your body.

For more information, please visit the following links, which will give you all the information you need on arthritis in your part of the world.

www.rheumatology.org.au, www.arthritis.ca, www.arthritis.org.nz, www.arthriticassociation.org.uk, www.arthritis.org.

 

Written by Sylvia McGrath, October, 2011

**Please note: that this e-book is just to serve as an information resource, this is not to be used for diagnosis. If you have any medical concerns or questions, please see your doctor for a proper diagnosis

 



Hydrocephalus

 

Hydrocephalus comes from two Greek words: ‘hydro’ meaning water and ‘cephalus’ meaning

head. Hydrocephalus was also commonly called ‘water on the brain’.

There are two types of Hydrocephalus, congenital (present at birth) and acquired (by injury,

trauma to the brain).

Our brains are surrounded by a fluid known as CSF, (cerebral spinal fluid), which is constantly

made and circulated. CSF is produced in the ventricles, circulates through the ventricular

system through the brain and is absorbed into the blood stream. It has many functions. It acts

as a protective cushion for the brain and spinal cord. CSF contains nutrients and proteins the

brain needs for nourishment and normal function and also carries waste away from the

surrounding tissue.

When there is a problem with absorbing the CSF into the bloodstream, it starts to build up in

the brain causing swelling. This swelling can lead to a multiple of symptoms including:

enlarged head (for babies), vision problems, lethargy, irritability, vomiting, headaches, balance

problems and memory issues. These symptoms are varied and varied in degree with each

individual.

Other problems that can be associated with hydrocephalus and they vary from person to

person. Some problems may be:

• Learning disabilities. Although individuals are able to learn, they may require special

modifications and assistance.

• Memory deficits

• Psychological deficits

• Motor Skill disabilities

• Vision problems

• Hearing difficulties,

• Seizures, and

• Hormonal imbalances.

• Sensitivity to sound, pressure and bright lights may also be associated with the

condition.

Because each case is individualized, generalizations in this category are difficult to make.

 

When not treated immediately, Hydrocephalus can permanently damage the brain and cause

physical and mental developmental problems. If untreated, it can be fatal.

CT Scan and/or MRI are the tests done to check for or confirm Hydrocephalus. These

machines take pictures of the brain and ventricles to show swelling, flow issues, blockages and

any other details that will help them determine the reason or cause of the symptoms.

Hydrocephalus is not curable, but treatable. Typically, shunts are used to treat

Hydrocephalus. A shunt is flexible tubing that is inserted into the ventricle(s) and then fed to

another region of the body, usually the abdominal cavity where the fluid can be absorbed. It

also can be fed to one of the heart chambers as well. At the ‘top’ of the shunt, in between the

skin and the skull a valve is placed, which regulates the CSF flow. The valve has a pressure

setting and once that pressure is reached, it kicks in and diverts the CSF to the other region

and the CSF is then absorbed there.

There is another treatment for Hydrocephalus called, Endoscopic Third Ventriculostomy

(ETV), but not everyone is a candidate for this procedure. You can find more information on

this procedure here: http://www.hydroassoc.org/education_support/faq#22

Shunts are still prone to issues. They can become infected and/or become blocked. If they

become infected, they are removed, replaced and treated with antibiotics. If they become

blocked, and there is no infection, the part that is blocked, can usually be replaced.

When an individual’s health has been good for a period of time, check up CT Scans are done

yearly (depending on individual) as well, a shunt survey, which is an x-ray to make sure there

is enough tubing in the abdominal cavity for growth. Depending on how quick the individual

grows, the need for lengthening will vary.

Hydrocephalus is treatable. Talk to your doctor if you have any concerns, they will refer you,

if necessary, to a neurosurgeon for further assessment and treatment.

Below, is some helpful information on Hydrocephalus.

*Please note, this article is not intended for diagnosis, please consult your doctor if you have any

comments, questions and/or concerns regarding yourself or an individual. This article is meant for

information purposes only.

 

Some of the information above and more can also be found at the following links.

Hydrocephalus Foundation Inc. – http://www.hydrocephalus.org/

910 Rear Broadway, Rt. 1

Saugus, MA 01906

Phone: 781-942-1161

Hydrocephalus Association – http://www.hydroassoc.org/

870 Market Street, Suite 705

San Francisco, CA 94102

Telephone: (415) 732-7040 / (888) 598-3789

Fax: (415) 732-7044

Medline Plushttp://www.nlm.nih.gov/medlineplus/hydrocephalus.html

Written by Renée MacLachlan: November/08

**Please note: that this e-book is just to serve as an information resource, this is not to be used for diagnosis. If you have any

medical concerns or questions, please see your doctor for a proper diagnosis.

“When the world says, “Give up,”

Hope whispers, “Try it one more time.”

~Author Unknown

Toronto Special Education – Summer fun.

http://http://www.examiner.com/toronto-special-education-in-national/toronto-special-education-summer-fun

Toronto Special Education: Summer Fun http://www.examiner.com School will soon be finished for the summer and thoughts go through parents minds of what to do with the children. For the parent of a special needs child it

Special Diets For Special Needs

When you or a member of your family have the need of special diets because of your illness or treatment, your doctor or registered dietitian may prescribe a special diet. They also may suggest a commercial product to help you meet your nutritional needs.

There are several special diets used during cancer treatment.  There are also products that can boost nutrition. We will list the links at the bottom of the page which will give you a variety of information you may need.  Remember that special diets and products to improve nutrition should be used only as recommended by your doctor or registered dietitian.

Special diets are an important tool for correcting nutritional problems that occur during cancer treatment. For example, a soft diet may be best if your mouth, throat, esophagus, or stomach is sore. Or, if your treatment makes it difficult for you to digest dairy products, you may need to follow a low-lactose diet. Some diets are well balanced and can be followed for long periods of time. However, some special diets should be followed for only a few days because they may not provide enough nutrients for the long term.

Only your doctor or registered dietitian should decide whether you need a special diet and for how long. If you are already following a special diet for another health problem, such as diabetes or high cholesterol, you and your doctor and registered dietitian should work together to develop your new plan.

The organizations we show after each chapter will also be able to assist you. For each illness, they will advise the diet, you require; they will give you a brief explanation of when the diet usually is recommended, the major foods it includes, and suggested meal plans. This information will help you follow the diet recommended by your doctor or registered dietician.

http://www.hc-sc.gc.ca/fn-an/food-guide-aliment/basics-base/index-eng.php

http://fnic.nal.usda.gov/nal_display/index.php?info_center=4&tax_level=2&tax_subject=256&topic_id=1348

http://www.caringforkids.cps.ca/index.htm

http://www.amazon.com/Special-Diets-Kids-Lisa-Lewis/dp/1885477449#reader

http://rex.nci.nih.gov/NCI_Pub_Interface/Eating_Hints/eatdiets.html

http://www.clicsargent.org.uk/Aboutchildhoodcancer/Forparents/Food/Specialdiets

Written by Sylvia McGrath, April, 2009

Funding Disabilities come in various shapes and forms. With them as well, comes the necessity at times for particular equipment, whether it is for communication, mobility, hearing, vision…etc. There are many resources available.

Here we have listed a few of the important resources available to apply to get funding to help cover the financial part of these necessities. Every family should have knowledge of these resources, the criteria and how to apply for them. Some resources are geared specifically for particular areas. Each has their own criteria of who can apply and how much is available.

 March of Dimes http://www.marchofdimes.ca

Ontario March of Dimes is the largest community-based rehabilitation and advocacy organization for people with physical disabilities in the province. Our goal is to enhance the independence and community participation of people with physical disabilities every day through a wide range of programs and services across the province.” Some of the programs March of Dimes offers are Acquired Brain Injury services, Assistive Devices, Attendant services, employment planning, and Home & vehicle modification to name just a few. HVMP (home and vehicle modification program) provides funding for basic home and/or vehicle modifications. Persons who meet the criteria can apply for grant funding of: -Up to $15,000 lifetime maximum for home modifications -Up to $15,000 every 10 years for vehicle modifications You can find more information on programs under programs and services on the website.

Easter Seals http://www.easterseals.org

“Easter Seals Ontario is dedicated to helping children, youth, and young adults with physical disabilities achieve their full individual potential and future independence. Easter Seals funds disability solutions through financial assistance, summer camp, the Recreational Choices Funding Program, research, advocacy, and public and consumer education.” Easter seals, offers programs in camp and recreation, direct financial assistance, feature scholarships and the Incontinence Supplies Grant Program. There is a cap or dollar limit per year, per client. That maximum is $3000.00 for equipment and other needs. You can find more information on these and other services by clicking Programs and Services on the website. The Incontinence Grant comes in three levels and helps offset the cost of diapers and/or supplies for persons who are incontinent. You are required to keep all your receipts from your purchases of diapers/supplies, as you may be called upon to present them periodically to review your costs and make sure you are in the correct level for the grant. The grant comes twice a year, in February and in August.

You can check out further information here, http://www.easterseals.org/services/?load=incontinence ADP – Assistive Devices Program: http://www.health.gov.on.ca/english/public/program/adp/adp_mn.html

“The objective of the Assistive Devices Program (ADP) is to provide consumer centered support and funding to Ontario residents who have long-term physical disabilities and to provide access to personalized Assistive devices appropriate for the individual’s basic needs.” “Devices covered by the program are intended to enable people with physical disabilities to increase their independence through access to Assistive devices responsive to their individual needs.”

“ADP covers over 8,000 separate pieces of equipment or supplies in the following categories: prostheses; wheelchairs/mobility aids and specialized seating systems; enteral feeding supplies; monitors and test strips for insulin-dependent diabetics (through an agreement with the Canadian Diabetes Association); insulin pumps and supplies for children; hearing aids; respiratory equipment; orthoses (braces, garments and pumps); visual and communication aids; oxygen and oxygen delivery equipment, such as concentrators, cylinders, liquid systems and related supplies, such as masks and tubing.”

 “Grants are provided for ostomy supplies, breast prostheses and for needles and syringes for insulin-dependent seniors.” Eligibility for ADP is any Ontario resident with a valid health card in their name and has a physical disability for a period of 6 months or longer. ADP covers up to 75% of the cost of certain equipment. For other equipment, there is a fixed amount. In most cases, the client pays a share of the cost and the rest is billed to ADP. If the client is not able to pay that share, there are other funding resources within their areas what will be willing to help cover the client’s portion such as, service clubs, social assistance, and even insurance companies.

You can acquire more information on their website if you require more specific information about any of their services. ACSD – Assistance for Children with Severe Disability http://www.gov.on.ca/children/english/programs/needs/disabilities/index.html

Parents with children with disabilities can also be eligible for this program. This assistance is to help parents cover some of the extra costs involved with raising a child with disabilities. Eligibility requires the child to be under 18 and has a severe disability.

This assistance also is based on income. Parents can receive $25 to a maximum of $410 to help with these costs. Other things taken into consideration are the severity of the disability and the kind of difficulties the child has doing personal care and everyday things.

Some of the costs covered could be:

  •  Travel to doctors and hospitals
  •  Special shoes and clothes
  •  Parental relief
  •  Wheelchair repairs
  •  Assistive devices
  •  Hearing aids
  •  Hearing aid batteries
  •  Prescription drugs
  •  Dental care
  •  Eyeglasses

 Some consideration is also provided for extra laundry being done in your household, if it is a result of taking care of the child and even special toys they require that would be beneficial to their ‘growth’. Contacting your regional office of the Ministry of children and youth services will get you an application form for ACSD. These are the most well known resources. There are many others out there available. Many cities will have particular organizations, clubs, legions, etc. that will help families meet the financial needs of ‘equipment’ necessities. Please do not hesitate to email us if you require information, or have any questions regarding the above information, we would be happy to help.

Written by: Renee MacLachlan – November/08

Special Olympics is humanity’s greatest classroom, where lessons of ability, acceptance and inclusion are taught on the fields of competition by our greatest teachers – the athletes”

 

Special Olympics Canada

http://www.specialolympics.ca/en/

Special Olympics International

http://specialolympics.org/

Special Olympics Ontario

http://www.specialolympicsontario.com/

 

MISSION STATEMENT

To provide year-round sports training and athletic competition for individuals with intellectual disabilities.

Special Olympics promotes opportunities to develop physical fitness, demonstrate courage, experience joy, and develop skills and friendship with their families, other Special Olympic athletes and the community.

Over the past 40 years Special Olympics has grown from a modest program serving local athletes to become the world’s largest movement dedicated to promoting respect, acceptance, inclusion, and human dignity for people with intellectual disabilities through sports.

~~~~~~~~~~~~~~~~~~~~~~

The purpose of this article is to bring attention and information of this great program that is available in most communities.  The benefits are great whether you are an athlete, coach, support staff or volunteer.  Your life will be enriched and forever changed.

Last summer, I had the wonderful opportunity to volunteer for the 2010 Special Olympics Summer Games held here in London, ON.  It was a time I’ll never forget!

London did an amazing job hosting and it showed in the faces and comments of the coaches, athletes and support staff.

The games created fun times and proud moments for the athletes, their teams and friends and family.  Many achieved goals, broke personal records and made new records for themselves and/or their teams.

Meeting so many wonderful people, athletes, coaches, support staff and other volunteers made this experience so amazing!  The athletes were the best!!

An Uncle of mine coaches a couple of the teams in Halifax.  When we have our family reunions they always consist of a softball game between the family and the athletes.  It’s something everyone looks forward to every year.  On top of that is a yearly BBQ my Uncle holds for them and many of the family are there to lend a hand in the preparations and happenings of the day.

There are 14 sports, and many Athletes do more than one!

http://info.specialolympicsontario.ca/programs-policies-procedures/14-sports

  • 5 Pin Bowling
  • 10 Pin Bowling
  • Alpine Skiing
  • Athletics (Track and Field)
  • Basketball
  • Bocce
  • Curling
  • Figure Skating
  • Floor Hockey
  • Golf
  • Nordic Skiing
  • Power-lifting
  • Rhythmic Gymnastics
  • Snowshoeing
  • Soccer
  • Softball
  • Speed Skating
  • Swimming

There are Regional, Provincial, National and World Games held.  Provincial Games are held on a rotating basis over a four-year period.  National Games are held every 2 years on a rotating basis. Athletes are selected from national competition to advance to World Games also held every two years on a rotating winter and summer basis.

Listed below are links to the District sites for Special Olympics, followed by a link to find Special Olympic programs by Community.

 

Central Ontario District http://central.specialolympicsontario.ca/

Eastern Ontario District http://east.specialolympicsontario.ca/

GTA District Sitehttp://gta.specialolympicsontario.ca/

Northern Ontario District http://north.specialolympicsontario.ca/

South Central District http://southcentral.specialolympicsontario.ca/

South West District http://southwest.specialolympicsontario.ca/

 

Special Olympic Programs by Community – http://directory.specialolympicsontario.ca/Community-Programs/

 

 

Special Olympics are proud to be affiliated with The Ontario Law Enforcement Torch Run.

http://www.torchrunontario.com/

The Ontario Law Enforcement Torch Run is a community-based, province-wide event that sees the “Flame of Hope” carried across Ontario by members of law enforcement agencies from across the province.  The objective of this and other events is to raise funds for and awareness of the Special Olympics movement in Ontario.

The Ontario Law Enforcement Torch Run is making a difference by raising funds for Special Olympics Ontario, and all funds raised are directed into community Special Olympics programs.  As well, the torch run involves law enforcement personnel in a community based, province wide program.  The torch run sets up community partnerships with sponsors, Special Olympics volunteers and local supporters, to reach a shared vision of helping athletes.

Special Olympics Ontario uses the funds raised to support three major initiatives:

  • Competition funding for communities hosting provincial and regional competitions, including travel and registration costs
  • Staff support, including SOO field staff
  • Support grants to new programs, competitions such as Hometown Games and programs in need, which amounts to approximately $250,000 per year

~~~~~~~~~~~~~~~~~~~~~~

The Special Olympics Programs are an amazing opportunity for youth and young adults to participate in a sport of their liking (some more than 1 or 2), make some great friendships, feel pride and accomplishment, attend some great social events, and enjoy new opportunities.

The joy and smiles on all of the Athletes faces is infectious and you can’t help but be taken in as you are surrounded by the warmth, happiness and pride!

Take a few moments to read some of the testimonials from the Athletes, coaches and family at the following link.

http://www.specialolympicsontario.com/default.asp?contentID=48

 

If you would like to become a volunteer for Special Olympics, here is where to start!

http://www.specialolympicsontario.com/default.asp?contentID=21

 

Facebook – http://www.facebook.com/specialolympicsontario

Youtube – http://www.youtube.com/specialolympicson

 

Irlen’s Syndrome

Initially call Scotopic Sensitivity Syndrome; Helen Irlen, an Educational Psychologist in the 1980’s, first identified Irlen’s Syndrome. Although the exact cause remains unknown, it is believed to originate in the retina of the eye or in the visual cortex of the brain. People with Irlen Syndrome tend to see words that are blurry, have patterns or appear to move on the page. The more the individual reads, the worse it seems to get. Coloured overlays and filters are used, because they appear to reduce the perceptual distortions and visual stress individuals experience.

Many people are unaware they have Irlen’s. It is most often confused for an optical problem. The problem is with processing, the inability, or weakness in processing visual information. It often is genetic and runs in families. It tends to go mis-diagnosed as a learning disability or dyslexia.

Symptoms of Irlen’s Syndrome can consist of the following:

  •  Trouble read words
  •  Weak concentration
  •  Headaches while reading
  •  Weaker academic performance
  •  Tires while reading
  •  Complains of eye strain while reading
  •  Depth perception is much weaker
  •  Often exhibits sensitivity to lights, especially fluorescent
  •  Can affect math performance
  •  Trouble focusing
  •  Weak or poor comprehension
  •  Reads in a strained word-by-word fashion and with hesitancy
  •  Difficulty tracking words on a line and often skip words
  •  Weaker written work
  •  Avoids reading
  •  Trouble copying
  •  Random letter sizes
  •  Random spacing
  •  Writing up or downhill
  •  Inconsistent spelling

 These symptoms are largely due to the fact that the print looks different to people with Irlen’s.

 Who can benefit?

Children and adults with reading and learning difficulties, low motivation, attention deficit disorder, or discipline problems are some of the people who can benefit from this service. Good readers and gifted students can benefit also.

 Testing

There is a 2-step process to identifying Irlen’s Syndrome, Problem identification, and Colour identification. Family members participate with their children in the evaluation. Colour, which is different for each person, is the key to the success of the program.

A certified, educational, professional trained person in the Irlen Method is required for an accurate diagnosis. Wearing the wrong colour can cause and/or worsen your problems.

Coloured lenses provided by and optometrist and/or vision specialist to treat reading problems are NOT the same as the Irlen Method. These professionals don’t have the right colours, or diagnostic process for colour selection. Inaccurate selection can result in headaches, eyestrain, and fragmented brain processing, resulting in more distortions and reading issues.

Find a centre near you: http://irlen.com/index.php?s=findclinic

Irlen’s Syndrome: http://irlen.com/

Irlen’s Syndrome: http://specialed.about.com/od/disabilities/a/Irlen.htm

Self-Tests: http://irlen.com/index.php?s=selftests

Written by Renee MacLachlan: March/09

**Please note: that this e-book is just to serve as an information resource, this is not to be used for diagnosis. If you have any medical concerns or questions, please see your doctor for a proper diagnosis.

Hepatitis

The most common cause of hepatitis (inflammation of the liver) is a viral infection. The cause of the infection can be anyone of several strains.

Hepatitis B Virus: can be found in some cases among newborn babies who may have been infected during birth if their mothers are carriers of the virus. In most cases if a baby is thought to be at risk are immunized against hepatitis B.

Hepatitis A Virus: This is the strain that most often the cause of hepatitis A virus in children. The hepatitis A virus is usually, caught by swallowing water or food that had been contaminated with infected feces.

If you or family members are planning a visit to any one of the developing countries where the disease is most prevalent, you may be, advised to be, immunized against this strain.

What is hepatitis C? Hepatitis C is a disease caused by a virus that infects the liver. In time, it can lead to permanent liver damage as well as cirrhosis, liver cancer, and liver failure. Many people do not know that they have hepatitis C until they already have some liver damage. This can take many years. Some people who get hepatitis C have it for a short time and then get better. This is called acute hepatitis C. However, most people who are infected with the virus go on to develop long-term, or chronic, hepatitis C.

Although hepatitis C can be very serious, most people can manage the disease and lead active, full lives.

Causes: Hepatitis C is caused by the hepatitis C virus. It is spread by contact with an infected person’s blood.

Symptoms:

Most people have no symptoms when they are first infected with the hepatitis C virus.

If you do develop symptoms, they may include:

  • Feeling very tired.
  • Joint pain.
  • Belly pain.
  • Itchy skin.
  • Sore muscles.
  • Dark urine.
  • Yellowish eyes and skin (jaundice). Jaundice usually appears only after other symptoms have started to go away.

Most people go on to develop chronic hepatitis C but still do not have symptoms. This makes it common for people to have hepatitis C for 15 years or longer before it is diagnosed.

Many people find out that they have the virus by accident, when their blood is tested before a blood donation or as part of a regular check-up. Often, people with hepatitis C will have high levels of liver enzymes in their blood.

If your doctor thinks you may have hepatitis C, he or she will talk to you about having a blood test. If the test shows hepatitis C antibodies, you have had hepatitis C at some point. A second test can tell if you have hepatitis C. treatments; you and your doctor need to decide if you should take antiviral medicine to treat hepatitis C.

It may not be right for everyone. If your liver damage is mild, you may not need medicine. If you do take medicine, the best treatment is a combination of two medicines that fight infection: peginterferon and ribavirin. How well these medicines work depends on how damaged your liver is, how much virus you have in your liver, and what type of hepatitis C you have.

Taking care of oneself is an important part of the treatment for hepatitis C. Some people with hepatitis C do not notice a change in the way they feel. Others feel tired, sick, or depressed. You may feel better if you exercise and eat healthy foods. To help prevent further liver damage, avoid alcohol and illegal drugs and certain medicines that can be hard on your liver.

For more information on Hepatitis please visit: Canadian Liver Foundation: Hepatitis A

http://www.liver.ca/Liver_Disease/Adult_Liver_Diseases/Hepatitis_A.aspx

The present report describes the status of hepatitis A in Canada. … Implications for hepatitis A vaccination policy in Canada:

Current hepatitis A status in Canada http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2094846

Prevention and treatment of different viral hepatitis diseases with links to fact sheets,

research – Hepatitis Public Health Agency of Canada – http://www.hc-sc.gc.ca/dc-ma/hep/index-eng.php

The Web Site of the American Liver Foundation – http://www.liverfoundation.org/education/info/hepatitisa

African Americans and Hepatitis C

American population with hepatitis C, compared with other groups infected with the virus. – http://www.hcvadvocate.org/hepatitis/factsheets_pdf/African_American.pdf

Hepatitis B – January 1, 2004 – American Family Physician

A patient information handout on hepatitis B, the American Association for the Study of

Liver Disease (AASLD) http://www.aafp.org/afp/20040101/75.html

Written by Sylvia McGrath, February 2009

**Please note: that this e-book is just to serve as an information resource, this is not to be used for diagnosis. If you have any medical concerns or questions, please see your doctor for a proper diagnosis

Heart

Heart arrhythmia, a common problem, is caused by the improper action of electrical impulses that are responsible for coordinating the heartbeats, by either causing the heart to race, flutter, and miss, or skip a beat.  Sometimes heart arrhythmia’s signs and symptoms can be quite bothersome and life threatening.  A damaged or weak heart can make arrhythmia worse and troublesome.

Medical technology advances have added new procedures, treatments and processes to eliminate or control the arrhythmia.  Changing to a heart healthy lifestyle will also assist in reducing the arrhythmia risk.

Heart failure (congestive heart failure) happens when the heart cannot pump enough blood to meet the body’s requirements.  Underlying conditions such as high blood pressure or coronary artery disease can leave the heart too stiff or weak to efficiently pump, by slowly sapping the heart of its strength.

Medications can improve symptoms and signs of chronic heart failure leading to survival but the condition cannot be reversed.  Like most chronic illnesses, heart failure can improve with the changing of lifestyle by eating healthy and exercise, which also improves the quality of life.

Mitral valve regurgitation (mitral valve prolapse) is a condition where the blood flows backwards into the heart.  This is caused by the mitral valve that does not close tightly.  When the valve does not work properly, the blood does not move through the body as efficiently as it should.

Mitral valve stenosis (mitral stenosis) with this disease the valve is blocked from opening properly and the blood flow is obstructed in the left chamber of the heart due to a condition where the heart mitral valve is narrowed.  With the narrowed mitral valve the blood is unable to flow efficiently through the heart onto the rest of the body.

Symptoms are similar for both valve problems

  • Fatigue
  • Shortness of breath

Treatments are similar for both mitral valve problems, the valve may have to be repaired or replaced and if left untreated can lead to serious heart complications.

Medications

Medications can calm the Mitral valve, which improves the symptoms and the survival rate.

Heart Murmurs are abnormal sounds during a heartbeat.  The sound is made by turbulent blood near the heart making a swishing or whooshing noise.  Most murmurs do not need treatment, as they are quite harmless.  These are called “innocent” murmurs and are often found in new babies and children.  In fact most children have heart murmurs at sometime during their lives.  In some children abnormal murmurs can be serious if they are due to congenital heart disease.  Abnormal murmurs in adults are usually caused by valve problems.

Treatments

1.  Innocent Heart Murmurs usually do not require treatment unless they are caused by hyperthyroidism or fever.  Once the condition is treated, the murmurs go away.

2.  Abnormal Heart Murmurs treatment is not usually given at first.  Depending on what is causing the heart problem the doctor will monitor the condition for a while and may prescribe either medication or surgery.

Signs and Symptoms

Although most people are not aware that they have a heart murmur, the following signs would prompt the doctor to order diagnostic tests.

  • Skin that turns blue on both lips and finger tips.
  • Swelling.
  • Shortness of breath.
  • Enlarged liver.
  • Enlarge neck veins
  • Poor appetite.
  • Weight gain.
  • Heavy sweating for no reason.
  • Chest pains.
  • Dizziness.
  • Fainting.

Medication

Depending on the type of heart condition, medications are given to ease or help the following symptoms.

  • To help your heart pump harder.
  • Prevent blood clots (which can cause blocked blood vessels).
  • Prevent fluid retention.
  • Lower blood pressure.

Surgery is used to

  • To patch a hole in the heart.
  • Fix a valve.
  • Rebuild blood vessels
  • Widen a narrow blood vessel.

Diagnostic Testing

  • When the murmurs happen.
  • The length of time they last.
  • The murmurs’ pitch: high, medium or low.
  • How loud a sound it makes
  • Where the heart is actually situated.

Additional Tests

  • Chest X-ray.
  • Electrocardiogram (ECG).
  • Echocardiogram.
  • Ultrasound.
  • Cardiac catheterization.
  • Endocarditic
  • Valve calcification.

 

 

 

 
For more information

www.heartandstroke.ca

www.bhf.org.uk,

www.americanheart.org,

 

Written by Sylvia McGrath, 2007

**Please note: that this is just to serve as an information resource, this is not to be used for diagnosis.  If you have any medical concerns or questions, please see your doctor for a proper diagnosis.

Hemophilia

Hemophilia is a genetic disorder that causes occurrences of spontaneous bleeding. Hemophilia can affect about one in ten thousand boys. This condition is caused by deficient activity of “factor vii,” a clotting factor in the blood. Girls who carry hemophilia gene have no symptoms; however, their sons may be infected by the disorder.

Symptoms:

Prolonged bleeding after an injury or minor surgical procedure; such as a tooth Extraction. Painful swelling of muscles and joints caused by the result of internal bleeding. The extent and frequency of bleeding vary extensively from one person to another. Some people suffer from only occasional period of minor bleeding. Others have extensive bleeding where there is the risk of damage to muscles caused by the internal bleeding.

Treatments:

Injections of “factor vii,” given by parents via drip – to treat bleeding episodes, in a severe case of bleeding the child may require to be admitted to hospital. “Factor vii” is in current use and is free of viruses such as HIV (The aids virus).

Outlook:

Children with Hemophilia should avoid hazardous activities, such as contact sports. As long as the “factor vii” is given, promptly when the bleeding occurs or regular infusions are given, muscles and joints may not be damaged and the life expectancy should be normal. For more information, please visit the following.

Canadian Hemophilia Society (CHS) Aims to improve the quality of life, for all persons with hemophilia and other inherited bleeding disorders and to find a cure. Also offers educational materials. www.hemophilia.ca

Hemophilia Federation of America: The vision of the Hemophilia Federation of America is that the bleeding disorders community has removed all barriers to both choice of treatment and quality of life www.hemophiliafed.org

 

Written by Sylvia McGrath, April, 2009

**Please note: that this e-book is just to serve as an information resource, this is not to be used for diagnosis. If you have any medical concerns or questions, please see your doctor for a proper diagnosis.