by Christy Winfree, M.S., Richard Williams, Ed.D., and
Gwynn M. Powell, Ph.D.
Since childhood cancer has evolved from an inevitably fatal illness to
a life-threatening chronic disease, children with cancer receive many positive
benefits by participating in a camp experience. These children can have
a variety of limitations, but first and foremost, they are still children
— and want to be treated the same as children without cancer with
opportunities to run, play, swim, and enjoy being with other kids.
The most frequent types of pediatric cancer include leukemia; tumors of
the central nervous system, sympathetic nervous system, kidneys, and bone;
and lymphoma (Bleyer, 1990). I changed the punctuation in this sentence
— before, it read like you could have a “tumor of lymphoma”
which according to Webster’s does not make sense. Is this change OK?
Because of the increase in long-term survival, quality-of-life issues have
taken a more prominent role in the comprehensive treatment for childhood
cancer. The trend in survivability has led to a shift in psychological emphasis
from crisis intervention and confronting death to facilitating and making
adjustments to a serious life-threatening chronic disease (Katz, Dolgin,
& Varni, 1990).
Chronic illnesses can be devastating to a person at any age. During childhood,
it can be especially destructive for the child’s psychological growth
and development. At a time when most children are deciding which sport to
play, pediatric cancer patients have their lives disrupted as they are faced
with harsh treatment methods such as chemotherapy and radiation in an attempt
to eradicate the cancer from their bodies.
A number of strategies have been used to reduce feelings of anxiety experienced
by pediatric cancer patients, including “diversions or activities
as means of catharsis” (Goertzel & Goertzel, 1991, p. 538). One
relatively new method that has been used to help children cope with their
terminal illness has been the development of summer camp programs designed
especially to meet their needs.
Children with cancer did not become involved in organized camping until
the late 1970s and early 1980s, because it was thought that the danger for
the children was too great and not worth the risk of additional pain or
injury. However, it has been recognized that the camp experience is very
valuable and can have positive impacts on all individuals. According to
the Children’s Oncology Camping Association (2002), there are currently
seventy-six camps that have been established to provide children with cancer
a chance to participate in the camp experience but more opportunities are
still needed.
Camp Rainbow is just one example of a camp program that has proven to be
an effective intervention for children with cancer. By making minor adjustments
(see Sidebar on page 30) to programs and providing children with recreational
activities, they are able to receive many benefits as well as learn coping
skills necessary to face the many issues brought on as a result of their
diagnosis and treatment process. Some of the critical issues that the camp
experience helps children address are:
- psychological effects of the disease;
- bodily changes;
- how they perceive themselves; and
- coping abilities of parents and siblings.
Psychological Effects as a Result of the Disease
One of the first issues that children with cancer face is how to adjust
psychologically and socially to living with this disease. As a result of
the progress in medical therapy, the psychological dilemma has been transformed
from one of adapting to death to coping with uncertain survival. According
to Bruneau (1981), a child with a potentially fatal disease undergoes psychological
reactions in four different stages:
- suspicion of having a serious disease, which leads to a sick child’s
identification with the staff and is shown as an eagerness to learn about
medical terms;
- aggression that comes from the child revolting against the disease
but realizing that there is no use;
- sinking into depression; and
- finally, experiencing feelings of grief.
Anxiety is a behavior that is commonly seen in all children with cancer
when they are diagnosed with cancer and becomes aware of the seriousness
of the disease (Kyngas, Mikkonen, Nousiainen, Rytilahti, Seppanen, Vaattovaara
& Jamsa, 2001). Researchers have concluded that children with cancer
experience significantly more anxiety related to the seriousness of their
illness than children with non-fatal chronic illnesses and that children
with cancer experience more anxiety during the progression of the disease
and with each clinic visit. Even when children are in remission, they can
still experience disease-related anxiety. It is this chronic uncertainty
about relapse and survival that poses a significant threat for the child
living with cancer. The amount of information children receive determines
the level of their anxiety and other psychological effects that they will
experience. If children are not told the truth about their disease, their
anxiety levels will increase. As a result, they will have unrealistic fantasies
leading to depression, withdrawal, and fear.
Thompson and Stanford (1981) reported a relationship between the decrease
in anxiety and the knowledge children with cancer gain about their disease.
Melman and Sanders (1986) concluded that children with an increased amount
of knowledge regarding their disease were able to contribute positively
to their psychosocial well-being.
Benefits of camp: reducing disease-related anxiety
Camps are effective modalities for reducing fear and anxiety in children
with cancer by providing opportunities where they can interact with other
children and learn ways to cope with cancer. A study by Bluebond-Langner,
Perkel, Goertzel, Nelson, & McGeary (1990) was designed to determine
whether cancer and its treatment were discussed informally among first-
time campers diagnosed with cancer. Results suggested that when such informal
discussions occurred there was a significant increase in the children’s
knowledge about cancer and its treatment. Perhaps the most important results
were an increased amount of knowledge in each group, especially in younger
campers. The study results confirmed that a large amount of free- flowing
conversation occurred between children regarding their type of cancer and
where they were being treated. Children in the study often introduced themselves
by the cancer they had and openly discussed side effects from treatments
and how they were coping with their illnesses. For most campers, having
opportunities to learn and acquire knowledge from other children who were
undergoing similar experiences was beneficial. It was reported that knowledge
of cancer was found to be positively related to self-image and aided in
better adjustment for the children attending the cancer camp.
Bodily Changes as a Result of the Disease and Treatment
Besides psychological effects, children with cancer also experience changes
in their physical appearance. The chemotherapy and radiation therapy that
a child undergoes has many harsh side effects. These side effects may be
reversible, such as weight gains or losses, loss of hair, and mouth ulcers,
or may be permanent such as amputation or skeletal abnormalities. The impact
of visible disfigurements, especially hair loss, is one of the most common
side effects of cancer treatment. The change in physi-cal image is a constant
reminder for children with cancer that they are different from other children.
The side effects of treatment continuously change the child’s body
image and often cause a loss of self-esteem for the child. This loss of
self-esteem can also lead to a lack of self-confidence resulting in regressive
behavior, a withdrawal from peers and a fear about going to school —
thus affecting their emotional and social adjustments, as well as their
academic performances. Children with physical disorders who experience this
disease and treatment-related changes in physical appearance are at a greater
risk for difficulties with peer relations and may face teasing, questions,
and comments from peers, in addition to relating their concern of feeling
different and unattractive. Participants in a study by Ross and Ross (1984)
reported that being teased on returning to school because of hair loss from
chemotherapy, weight gain from medicines, or weight loss from the disease
was worse than physical pain from the disease and treatment procedures.
During the childhood years, physical appearance and social acceptance are
important predictors of adjustment. Varni, Katz, Colegrove, and Dolgin (1995)
concluded that higher perceived physical appearance predicted lower depressive
and anxious symptoms and higher general self-esteem.
Benefits of camp: bodily changes
When children are able to interact with others like themselves, they are
able to realize that they are not alone. Camps can offer children with cancer
the opportunity to interact with peers who accept their limitations as well
as with others who have or are experiencing similar physical changes. Children
are able to tell each other what treatments they have undergone, the physical
changes that resulted, and ways they are coping with the changes. Opportunities
such as these allow children with cancer to discover interests, enhance
skills, and develop a greater respect for themselves and their abilities
(Varni, et al., 1995). According to research, when chil-dren with cancer
attend camp, they develop better self-concepts and enhance their self-esteem.
These changes allow chil-dren to deal more effectively with comments that
they will face from peers at school, thus enabling them to fit into their
social environment, as well as enhance academic performance (Melman &
Sanders, 1986). When children feel competent, they are able to feel good
about themselves, interact with others, and be less anxious (Children’s
Oncology Camps of America, 2002).
Change in the Child/Adolescent’s Perception of Self
as a Result of the Disease
The new role of being sick or different involves a change in nearly every
aspect of the child’s life. Children will experience a change in their
relationship with other people and in their perception of themselves. The
illness also causes major developmental changes in the areas of control
and competence. This developmental change is a factor that must be managed
in order for children and adolescents to have greater control of self and
autonomy. The illness deprives the child of control of daily routine, privacy,
relationships with family and friends, and control of life itself. When
children and adolescents feel in control, they are motivated to take better
care of themselves. This concept is known as locus of control. According
to this theory, individuals differ in their beliefs about their ability
to take active steps to promote their own health. Individuals with an internal
locus of control are more likely to take positive steps to control their
health behaviors and to experience less anxiety. Research by Goertzel and
Goertzel (1991) focused on children’s self-concept, locus of control,
and level of anxiety. Participants ranged in age from eight to eighteen,
had a diagnosis of leukemia, and were all outpatients who attended the American
Cancer Society Camp. The results suggested that an individual could do a
great deal to control his/her personal health and showed that they were
able to decrease their levels of anxiety through participating in activities
such as sports, gardening, talking to friends, drawing, and receiving support
from family and friends.
Benefits of camps: self-perception
For children with cancer, camps can provide both support and opportunities
to be in control of their experiences. By choosing the activities in which
they wish to participate, they are able to gain a sense of normalcy. It
is important for camps to allow campers these opportunities, since many
children and adolescents have come from environments where they have little
independence as a result of their many hospitalizations and protective parents.
When children and adolescents are given this freedom, they are able to participate
in activities that help them master their feelings and gain a greater sense
of autonomy. Bates (1984) conducted research on eighty-four campers with
a variety of disabilities including cerebral palsy, sickle cell anemia,
brain tumors, diabetes, asthma, and congenital defects to determine how
a camp experience affected their lives. It was reported that an increase
in self-esteem resulting from camp better prepared these children to compete
in society. In addition, it was concluded that camp is a learning and enriching
experience for all who participate. When children go to camp, they learn
to be more independent and acquire social skills. Furthermore, it was noted
that the positive view of self and life gained during camp experiences ultimately
reduces an individual’s dependence on others.
Coping Abilities of Parents and Siblings as a Result of
a Cancer Diagnosis
A final issue with which children with cancer have to deal is the way their
parents and siblings react to and cope with their diagnoses. The disease
can have both positive and negative effects for each family member —
especially the child with cancer — depending on parents’ perception
and coping abilities. Researchers have concluded that anxiety, grief, anger,
hostility, guilt, and disbelief are the responses most often observed in
parents (Kyngas et al., 2001). Parents’ reactions to the disease not
only influence their own approach to parenting but place extra demands on
their parenting skills. For example, parents are faced with the role of
having to talk with their child about the disease, support the child, take
care of the child’s physical condition, and prepare the child for
death as well as living. Although parents are advised to treat their child
as normally as possible, many parents overprotect and overindulge their
child. When this occurs, children are either brought up in environments
where there are too many rules limiting their independence or environments
where no structure is provided. The child’s cancer treatments can
also disrupt the family routine and lifestyle, requiring a change in family
rules, goals, and expectations for the future. Anxiety and depression often
occur in as many as 50 percent of these parents — with most of these
symptoms disappearing during the treatment phase.
An increasing amount of attention is being given to the emotional problems
shown in siblings of children with cancer. Parents have often reported that
their healthy children displayed symptoms of irritability, feelings of guilt
and jealousy, academic underachievement, and behaviors of acting-out. Also,
during this time, siblings reported feeling the loss of a close relationship
with their parents and feeling isolated from supportive systems outside
the family. These feelings of isolation, guilt, and jealousy may be aggravated
when siblings have not received reliable information to explain the change
in parental attitude. Often families have not discussed the disease or have
given insufficient information about the disease to the siblings. Siblings
must be made aware of what is happening to their brother or sister who has
cancer and have their concerns discussed and validated. Also, siblings must
be made to feel they are important and can play effective roles in helping
their brother or sister get through their treatments.
Benefits of camp: parents and siblings
Camps are able to provide benefits to all family members. Camps provide
parents with respite assurance that their child is in a safe environment.
While children are at camp, they can gain independence from parents, meet
friends, develop new skills, and discover new interests by participating
in activities that may not have been available at home (e.g., canoeing,
sailing, swimming). Some camps even offer special support programs for parents
to attend at the same time as their child. These programs provide opportunities
for parents to relax, gain support from other parents, and spend quality
time with their child in a fun environment. According to the Children’s
Oncology Camping Association (2002), there are camps that have been created
so that both children with cancer and their siblings can attend. Studies
on these types of camps have found that children with cancer and their siblings
are able to connect in a “normal” environment by participating
in activities together, thus resulting in the formation of a stronger bond.
Siblings also gain support from other siblings who are experiencing the
same things they are going through. Through the camp experience, siblings
are able to discover they are not alone, are able to have their feelings
validated, and discover effective ways to cope.
A Beneficial Environment
Overall, camps have proven to be a beneficial environment for all children
— especially those with cancer. Through the camp experience, they
can learn many of the skills necessary to meet the extraordinary challenges
that they will face while fighting their disease and the everyday struggles
of life. Camp allows children with the cancer the opportunity to be themselves
by allowing the focus to be off of their disease and on meeting friends,
swimming, sailing, horseback riding, and making crafts. By participating
in enriching camp experiences, these children are able to gain confidence
in themselves and learn activities that they can carry with them throughout
their lives. While at camp, children are able to develop skills and abilities
as well as see that they are still able to do many of the same activities
as everyone else. Camp directors need only to examine their current programs
and discuss possible modifications with staff in order to incorporate children
with cancer into their programs. Cancer need not be a limitation that prevents
children from being children. In essence, we all have limitations, but with
the proper support we are able to overcome obstacles, learn ways to cope,
and develop the necessary skills for adapting to any circumstance we face.
References
American Camping Association, (2002). Research.
Bates, E. A. (1986). Project gateway. Camping Magazine, 40, 28-31.
Bluebond-Langner, M., Perkel, D., Gorertzel, T., Nelson, K., & McGeary,
J. (1990).
Children’s knowledge of cancer and its treatment: Impact of an oncology
camp experience. The Journal of Pediatrics, 116, 207-213.
Bruneau, J.P.(1981). Soins infirmiers dans la dimension psychologique
de l’enfant mourant. Soins 26, 79-87.
Children’s Oncology Camping Association (2002). Research.
Goertzel, L., & Goertzel, T. (1991). Health locus of control, self-concept,
and anxiety in pediatric cancer patients. Psychological Reports, 68, 531-540.
Katz, E. R., Dolgin M. J., & Varni, J.W. (1990). Cancer in childhood
and adolescents. In Gross, A. .M., and Drabman, R. S. (eds.), Handbook
of Clinical Behavioral Pediatrics, Plenum, New York, 129-146.
Kyngas, H., Mikkonen, R., Nousiainen, E. M.; Rytilahti, M., Seppanen,
P., Vaattovaara, R., & Jamsa, T. (2001). Coping with the onset of
cancer: Coping strategies and resources of young people with cancer. European
Journal of Cancer Care, 10 (1), 6-12.
Melman, J. E., & Sanders, J.A. (1986). Psychosocial aspects of childhood
cancer: A review of the literature. Journal of Child Psychiatry, 27, 145-167.
National Cancer Institute (2001). Research.
Ross, D.M., & Ross, S.A. (1984). Stress reduction procedures for the
school-age hospitalized leukemic child. Pediatric Nursing, 10, 393- 395.
Thompson, R. H. & Stanford, G. (1981). Child life in hospitals: Theory
and practice. (2nd ed.). Springfield, Ill.: Thomas Publishers, Inc.
Varni, J.W., Katz, E. R., Colegrove, R., & Dolgin, M. (1995). Perceived
physical appearance and adjustment of children with newly diagnosed cancer:
A path analytic model. Journal of Behavioral Medicine, 18, 261-278. |
Originally published in the 2002 November/December
issue of Camping Magazine.
|