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Psychosocial Aspects

How can I deal with financial difficulties?

Severe symptoms of HCV or the side effects of treatment may affect your ability to work. You may find you could use some form of income assistance. Depending on your circumstances, you may be able to collect benefits from the following places:

  • Human Resources Development Canada Employment Insurance (EI): Benefits are calculated based on the number of hours worked. Applicants for EI Sickness Benefits must have a minimum of 600 hours of insurable work in the past 52 weeks. If you provide medical proof of illness, Sickness Benefits will last for 15 weeks. EI also offers retraining programs if illness prevents you from keeping your current position.
  • Canada Pension Plan (CPP) and Quebec Pension Plan(QPP): If you have paid CPP/QPP premiums, you may qualify for a disability pension. Eligibility is based on the number of years you have contributed and a detailed medical assessment you must submit to indicate your condition is both “severe and prolonged.”
  • Social Assistance: Your local welfare office may provide you with financial assistance for shelter, living expenses and essential medical needs. Eligibility for a disability pension varies among provinces/territories.
  • Employee Benefits Package: A disability pension paid out by a private insurance company may be available through your employer. Check with your personnel department or union representative for specific plan details.

What is the impact of HCV on family relations?

Family relationships may be affected by HCV even if you do not have symptoms. At first there may be tension or friction between family members because it takes time for some  people to adjust to even small changes in lifestyle. Be sure to keep communication open and try to maintain usual family activities. A counsellor may be able to help.

How do I tell my children that I have HCV?

There may be visible effects of HCV or the treatment, and changes in your life that children will pick up on. Your children may actually experience more worry from not knowing what is wrong than from knowing the truth. If you decide to tell your children about HCV, do so honestly and directly.
  • Carefully choose a time to tell your children.
  • Tailor explanations to suit the ages of your children. Be prepared to reassure them if they ask about death.
  • If children avoid the subject, provide information in a non-threatening way such as leaving a booklet on the table.
  • Just like you, children of all ages need reassurance and information. It takes time to adjust, so be patient with them and yourself.

As a parent, how can I help my teenager with HCV?

Teenagers tend to think of the present and believe that nothing bad can happen to them. They also tend to have a strong desire to show independence. A lack of symptoms and the desire to fit in with friends may result in risky behaviour. These are all obstacles to getting your teenager to understand the possible long-term effects of HCV.
  • Promote healthy options for personal exploration, e.g., sports, arts, hobbies.
  • Encourage your teenager to talk to you or someone supportive about his/her feelings.
  • Avoid overprotecting your teenager.

How can I support a family member or friend with HCV?

Having a network of people who are socially supportive is important because it helps to buffer or moderate the effects of stress on physical and mental health. Your friend or family member will cope better if information, emotional support and practical assistance are available when needed.
  • Learn about HCV.
  • Avoid judging the person.
  • Listen to the person before trying to take over. It allows the person to express what he/she needs, wants and expects from you. You’ll see where you fit in.
  • Expect the person’s mood and outlook to vary.
  • Reinforce hope and optimism.
  • Try not to neglect other relationships.
  • Take care of yourself and talk to your own supportive people.

As a young man with hemophilia, how will HCV affect me?

It is difficult to feel different and usually very hard to say no to your friends if they are experimenting with alcohol, drugs and sex. Having HCV, with or without HIV, can have an impact on your lifestyle and self-esteem. To protect your health:
  • Do your best to follow the treatment plans for each diagnosis (e.g. hemophilia, HCV, and possibly HIV and arthritis).
  • Avoid risky behaviour such as drinking at parties.
  • Practice safer sex. Although HCV is rarely transmitted sexually, you may wish to consider telling anyone with whom you had unsafe sex. Your present partner(s) may also want to get tested.
  • Learn how to correctly interpret symptoms. The musclepain associated with interferon may feel like a bleed, or a bleed may be mistaken as a side effect of treatment.
  • Get vaccinated for both hepatitis A and hepatitis B. There is evidence that hepatitis A can cause worsening of liver disease if you already have HCV. If you were born after1983 you probably have been immunized against hepatitis B.

What emotions can people with HCV experience?

If you are living with HCV you may feel as if you have lost something in life due to changes in health, routine and perhaps your vision of the future. The emotions you and your family experience may mirror those felt by people going through a grieving process. Grieving is usually associated with death but people diagnosed with HCV (and other illnesses) can feel grief too, due to the sense of loss.

The following steps may not occur in this order, but they will likely touch your life at some point.

  • Shock and denial. You may feel so numb that you act as if nothing has happened. This may help you cope initially as a sort of anaesthesia, but can become a problem if you don’t take care of yourself (e.g., drinking instead of avoiding alcohol, and not seeing a health care provider).
  • Emotions erupt. Your emotions may break out in heavy sighs or crying spells as you become more aware of your painful loss.
  • Loneliness. You may withdraw from others that you feel “don’t understand.”
  • Illness. Your body may temporarily break down due to this new stress in your life.
  • Panic. You may not feel like your old self, or you might wonder “How will I manage?” This panic should pass.
  • Guilt. With no ready answer on who or what was responsible for the HCV infection, you blame yourself. This will naturally lead to feelings of guilt or even anger at yourself.
  • Depression. Commonly precipitated by feelings of isolation, hurt and sadness.
  • Anger. Precipitated by the unfairness of your loss, your anger may be directed at your health care team, those close to you, God.
  • Difficulty adjusting to a new situation. You may resist letting go of your attachment to the past. You may consequently withdraw further into yourself in an attempt to analyze your own thoughts and emotions.
  • Hope. Eventually breaks through and begins to grow again.
  • Affirming reality. Involves reconstructing your life using the resiliency and strengths you have learned you possess when experiencing the grieving process. You adjust to any limitations, set new goals, and learn to appreciate your new life.

How can I deal with my feelings?

  • Go ahead, feel what you feel. Don’t tell yourself that a particular feeling is bad or try to pretend it’s not there. Your feelings are natural and you have a right to them. They can even help you move on to a more comfortable state of mind.
  • Recognize your feelings. What are you actually feeling? Sometimes one emotion is covering up a different emotion. For example, sadness might cover up feelings of anger; anxiety might indicate excitement. Admitting to yourself “I’m angry” or “I’m scared” is a big step toward coming to terms with your feelings.
  • Get to know what triggers your feelings. What led up to the feeling? Do some people, situations or anniversary dates create a certain feeling in you?
  • Express your feeling and then let it go. You might fear alienating friends and family, but repressed feelings can fester and grow. “Bottling” up anger, for example, can result in excessive bitterness. Expressing your feelings can be done in constructive ways that cause no damage to yourself or others. Examples include crying, talking with others, or writing in a journal.
  • Try to be as active as you can. Activities that hold your interest will help keep your mind off fears, depression and worry. Look for people and situations in which you can invest your love and energy.
  • Reward yourself. Give yourself something pleasant to anticipate. Set aside at least 15 minutes daily to do something you really enjoy.

How can I get emotional support?

Living with HCV can cause emotional responses that you may need help dealing with. It’s not unusual to feel stressed or depressed. At those times some people may only feel comfortable talking to a family member or friend. Others may prefer to consult with a qualified therapist. There may be a local support group or organization that can arrange to have you meet others with HCV.