Do you have a family member with cancer?
Grants- Families that qualify are awarded grants to help with the financial burden cancer places on nearly every family. We typically
follow a family through their treatment plan and award multiple grants when we see a need.
Support - Sometimes we just need to know that the way we are feeling is normal. Talking to another family that has gone through
something very similar can help. Each type of cancer and stage brings different treatment. We connect families with others
that have gone through, or are going through, a similar treatment plan.
Raising Money- We help families set up pages on Facebook, Go Fund Me, other forms of social media, and crowd funding.
Fundraisers- We help families plan fundraisers. We can utilize our non-profit status and receive donations on behalf of cancer families.
Coping- Grieving is a normal response to a loss. The loss can include the loss of your previously healthy child, the loss of your normal
daily routine, the impact of the diagnosis on other family members, and the financial impact of the diagnosis. The grieving process
varies from person to person in terms of the order in which one experiences the stages of grief, as well as the time it takes to go
through the grief process. We are a shoulder to lean on through every step.
Other Resources Available- Many families end up in hospitals far away from home. Family members might need travel money or a
place to stay. Many family members need help covering the mortgage or rent on their home while they spend time with their child. Some
families need meals for themselves or other family that is still at home. Each type of cancer is different and so are the resources. Many
non-profits offer grants for specific types of cancer.We notify families on the resources that are available.
Coping with a Diagnosis of Cancer in Children
Learning that your child has cancer usually makes parents feel like their world has been turned upside down. Everything in their life may suddenly feel out of control. Your initial thoughts may be "How could this have happened to my child?" and "How will we get through this?"
A cancer diagnosis is shocking and overwhelming, particularly in children. However, prognosis of childhood cancer continues to improve, and the chance of being cured continues to increase.
Grief is usually divided into five stages:
Denial. Denial is a stage where people try to believe that the cancer diagnosis is not happening to them, their child, or their family. One may feel numb, or in a state of shock. Denial is a protective emotion when a life event is too overwhelming to deal with all at once. It is normal, and is not a problem unless it stands in the way of getting the child needed medical care.
Anger. Anger is a stage in which you understand the cancer diagnosis and are very upset and angry that it has happened in your family. One of the best ways of dealing with bursts of anger is to exercise or participate in another type of physical activity. Talking with family and friends, other parents who have a child with cancer, and the hospital staff, may also be helpful. The child also needs to be able to express his or her anger by therapeutic play, talking to other children, drawing pictures of how they feel, or writing in a journal.
Bargaining. Questioning God, asking "Why my child?" and "What did we do to deserve this?" are common questions in this stage. It is normal for parents to make bargains with themselves or God, in hopes that this will make the cancer diagnosis go away. Guilt is a primary emotion during this stage. Searching for something that you personally did, which could have contributed to the cancer in your child, is all part of bargaining. Parents tell themselves or God that they promise not to do something they previously did (such as arguing with family members), or to start doing something they have not done (such as going to church regularly), in exchange for their child's cancer recovery. It is important to remember that there is nothing that you or your child did which contributed to the cancer. It is no one's fault.
Depression or sadness. This is a stage in which the diagnosis of cancer can no longer be denied and parents and children may feel a profound sense of sadness. This is normal. It can be accompanied by physical changes, such as trouble sleeping, or excessive sleeping, changes in appetite, difficulty with concentrating on simple daily activities, or feeling a constant fear that someone else in the family will be diagnosed with cancer. It is important to talk about depression with a healthcare professional, such as a social worker or counselor, or meet with a support group to help you cope with these feelings.
Acceptance. Acceptance is a stage in which you have accepted the cancer diagnosis and are at a point where cancer has been incorporated as part of your life. You have made an adjustment to your child's illness. This does not mean that you will never feel other emotions, but usually families find that they are better able to manage their lives overall once they reach this stage.
Going through the grieving process is the best way to cope with a cancer diagnosis. You may find yourself moving in and out of the various stages as your family goes through the cancer experience. By giving yourself, your child, and your family permission to do this, you will be able to cope.Coping with the diagnosis
Some practical things that you can do to help during this time include the following:
Learn as much as possible about your child's disease. At times, ignorance or a lack of understanding is your worst enemy. Arm yourself with information in order to lessen frustration. Do not hesitate to ask questions about your child's disease. You may wish to keep a notebook with all of the medical records and information about your child's diagnosis. Sometimes, parents can be too numb or too upset while at the hospital or healthcare provider's office with their child and realize later that they forgot everything the healthcare provider had said. Write things down. You may even want to talk to the healthcare provider about recording your conversations so you can review them later.
Keep a journal of your feelings about your child's disease and the impact on your life. As time goes on, you will be able to look back and see that things are improving and that you are moving forward, even though at times it may not seem so.
Learn about your health insurance benefits. This way you will understand what expenses will be covered and what you may have to pay.
Continue doing at least some of your usual, daily activities. You will still have grocery shopping, laundry, and going through the mail to do on a daily or weekly basis. Having some of these "regular" activities will help you cope and feel more in control. Using a cell phone to communicate with the hospital is one way to accomplish these activities and still be in touch with what is happening with your child.
Take care of your family relationships. Although your primary focus is on your child with cancer, it is important to also spend time as you normally would with your other children and your spouse. It is healthy to have fun together, even when a child in the family has cancer. Relieving stress and strengthening family relationships will help all of you cope better with your child's disease.
Use support groups in the area, as well as national support groups and their resources. Find out about supportive services available at the hospital to help you cope, such as the availability of social workers and/or meeting with other families. Do not be afraid to ask for help. Each family's need for support is unique. Friends and family members will often ask "Is there anything I can do to help?" Consider saying "yes" to this question and ask them to pick up your groceries, help with the laundry or housecleaning, pick up your other children from their extracurricular activities, or make dinner. "Assigning" a friend or family member something to do to help you will also help them feel like they are contributing.
Avoid emotionally draining situations. Sometimes, well-meaning friends and family members will say the worst possible thing at the time of a cancer diagnosis. They truly want to help or be supportive, but sometimes do not know how to respond. Their words may hurt you or disappoint you, even though that was not their intention. You must realize that people will not know what your needs are unless you tell them. Sometimes, it is simply easier to be forthright and tell someone "I would just like you to sit quietly with me and keep me company" or "I need to spend some time alone right now." Do not be afraid to express your needs during this time.
Other parents or acquaintances may want to talk to you about their experiences with cancer. They may believe that they are being helpful to you, but instead may be making your situation feel even more overwhelming. It is important for you to avoid these discussions if they are not helping you. It is healthy to be "selfish" and ask for what you need, as well as what you do not need during this time.
Share what you have learned. You will have important knowledge and skills that you learn as you experience your child's illness. You could help other parents and their families by sharing your experiences in a support group or other setting.
The following is a list of suggestions for patients, parents, and siblings that may help each individual cope with his or her emotions, depending on the age of the child with cancer and the age of the siblings:
Infants and very young children (birth to 3 years of age):
Distracting with toys or colorful objects
Creating a cheerful, hospital room
Having siblings visit
Keeping their regular schedule for sleeping and feeding
Arranging visits to ill brother or sister
Keeping them near parents, if possible
Using relatives, friends, or a daycare center to maintain their usual daily routine
Having one parent spend time with them daily
Recording lullabies, stories, messages when parent cannot be at home
Offering reassurance often to toddlers that mommy or daddy will soon be back
Toddlers, preschool (3 to 5 years of age):
Giving very simple and repeated explanations for what is happening
Providing comfort when child is upset or fearful
Checking on child's understanding of what is happening
Offering choices when possible
Teaching acceptable expression of angry feelings
Maintaining a normal daily schedule for feeding and sleeping
Giving simple explanation for parent's distress, sadness, or crying
Giving a simple explanation that brother or sister is sick and that people are helping
Offering comfort and reassurance about parent's absence
Arranging for reliable daily care and maintenance of usual routines
Having one parent see child daily, if possible
Remaining alert to changes in behavior
Reassuring child about parent's distress or sadness
School-aged children (6 to 12 years of age):
Offering repeated reassurance to your child that he or she is not responsible for the cancer
Teaching that sadness, anger, and guilt are normal feelings
Allowing your child to keep feelings private, if that is preferred
Suggesting personal recording of thoughts, feelings through writing, drawing
Arranging for physical activity, when possible
Providing explanations your child can understand about diagnosis and treatment plan; including your child, when appropriate, in discussions about diagnosis and treatment
Answering all questions honestly and in understandable language, including, "Am I going to die?" (talk with cancer care team about how to answer)
Listening for unasked questions
Facilitating communication with siblings, friends, and classmates, if desired
Arranging contact with other patients to see how they have dealt with diagnosis
Teaching about normal feelings of fear, anxiety, sadness, or anger
Encouraging sibling to communicate feelings; suggesting sibling write, telephone, send drawings or recorded messages to patient
Providing understandable information about diagnosis and treatment
Answering all questions honestly, including, "Will he or she die?"
Listening for unasked questions, especially about personal health
Offering repeated reassurance that sibling is not responsible for causing the cancer
Informing teachers and coaches of family situation
Arranging for school and other activities to continue on schedule
Supporting sibling's having fun, despite brother or sister's illness
Planning for daily availability of one parent
Explaining that parents' distress, sadness, or crying is okay
Adolescents (13 to 18 years of age and older):
Giving information on normal emotional reactions to a cancer diagnosis
Encouraging expression of feelings to someone: parents, family, or staff
Tolerating any reluctance to communicate thoughts and feelings
Providing repeated reassurance that they are not responsible for causing the cancer
Being included in all discussions with parents about diagnosis and treatment planning
Being encouraged to ask questions (parents should listen for unasked questions)
Addressing spiritual concerns about "Why me?"
Permitting private time for interaction with team professionals
Offering assurance that parents and family members will be able to manage crisis
Encouraging sharing news of diagnosis with peers, and classmates
Arranging for visits of siblings and friends
Facilitating contact with other adolescent patients, if desired
Involving adolescent in events around diagnosis
Reassuring that cancer is not contagious
Offering assurance that nothing they did or said caused the cancer
Providing detailed information on diagnosis and treatment plan
Answering all questions honestly
Arranging access to treatment team, if desired
Discussing spiritual issues related to diagnosis
Encouraging expression of feelings
Arranging for management of daily life at home
Providing assurance that family will be able to handle crisis
Informing teachers and coaches of family situation
Encouraging usual involvement in school and other activities
Asking relative or friend to take a special interest in each adolescent sibling
The various members of the cancer team can assist your family, as needed. The seriousness of a cancer diagnosis and the difficulties of treatment cannot be forgotten.
- Levy, Adam S., MD
- Ziegler, Olivia, MS, PA