How can I help?
There is so much you can do to help, if and when you are
needed.
Learning about the symptoms and any side
effects of treatment your loved one might have means you can
better understand what is happening to them and their
behaviour.
Help upon diagnosis
You may feel shell-shocked, angry or confused when you find
out someone you care for has Hepatitis C. It is common to feel
a whole range of emotions, at the time and later on once the
information has had the chance to sink in. There is no right way or
wrong way to deal with the news, everyone handles things
differently.
It is important to remember that many people have Hepatitis C
and treatment is available, meaning it is possible to clear the
virus. Try to help both of you to stay calm and be positive, there
are many things you can do together to slow down the disease to reduce the effect of the
virus. There are also people you can speak to so both of you
can find out more about the virus, treatment and to talk things through.
Help during treatment
Most patients do not suffer symptoms from the illness itself,
at least not for many years. It is however, common to suffer side
effects whilst on treatment. These can include forgetfulness,
confusion, depression, stress and mood swings. There can also be
physical effects such as exhaustion and loss of appetite, and flu
like aches and pains. This may have a knock on effect on your
relationship, finances, loss of libido or some changes in lifestyle
e.g. diet. Knowing it's the virus or side effects that cause this
can help understanding and lessen frustrations. Side effects will
vary depending on the person and which drugs you are prescribed.
New drugs mean treatment durations are also reducing.
Support for families and carers
Supporting someone through any serious illness can be very
demanding. At times you may feel tired yourself, as well as
emotionally drained. This is well recognised, so contact a support
organisation or helpline to speak to someone if you need
help.