With the new school year well underway, many kids are excited to go back. At the same time, some NF kids may face some social and behavioral issues. Let's revisit our interview with the University of Wisconsin-Milwaukee Psychology Department's Kelly Janke, M.S., to learn more about learning issues and NF children.
Tuesday, October 9, 2012
Back to School and NF Kids
With the new school year well underway, many kids are excited to go back. At the same time, some NF kids may face some social and behavioral issues. Let's revisit our interview with the University of Wisconsin-Milwaukee Psychology Department's Kelly Janke, M.S., to learn more about learning issues and NF children.
Monday, March 19, 2012
Little Sends Lots of Letters of Support
Since 1996, the Department of Defense’s (DOD) funding of the Neurofibromatosis Research Program (NFRP) has made important contributions helping people not only with NF but it also translates to cardiovascular, learning disabilities, war-related injuries, and other illnesses. The Littlest Tumor Foundation advocates keeping the research for NF ongoing. In order keep the DOD’s funding for the research going, the Littlest Tumor Foundation asked people throughout northeastern Wisconsin and beyond to sign a letter of support letting both the U.S. Congress and Senate that people wanted the research to continue. We went to the University of Wisconsin’s Oshkosh and Green Bay campuses collecting signatures of support and spreading the word about neurofibromatosis to students and others. Many people had not even heard of NF but when they did they were more than eager to sign the letter of support to potentially impact 175 million people. We had even met people who have NF as well!
After collecting the signatures, we sent out letters of support to our congressional representatives from the eight Wisconsin districts. We were able to meet with every congressional office and sentorial aide in both Washington D.C. and Wisconsin. When we got back in the Fox Valley region of Wisconsin, we had face-to-face appointments with Rep. Tom Petri in Fond du Lac, Rep. Reid Ribble and Tony, Senator Ron Johnson’s aide. At the meetings we discussed the importance of the DOD’s NF research and how it would impact millions of people in the US and abroad as well as raising awareness about NF. Since the sending of the letters of support and meetings, Representatives Reid Ribble, District 8, Gwen Moore, District 4, Tammy Baldwin, District 12, and Thomas Petri, District 6, have signed the letter. Thank you all who have taken a little time to sign the letter of support to continue the Neurofibromatosis Research program, our hard work has paid off thanks to you! In the end, we sent out 2,822 letters of support.
Wednesday, February 29, 2012
Interview with Kelly Janke, M.S., researcher of NF children and learning issues

NF not only causes issues in terms of tumors on the body and other medical ills, but also learning issues. Please read the following interview with Department of Psychology's Kelly Janke, M.S., of the University of Wisconsin-Milwaukee to learn more about learning issues and NF children.
1. Discuss some of the learning issues that you have seen with NF children in school.
Children with NF-1 are more likely to have learning difficulties than their siblings or same-age classmates who do not have NF-1. The rates of learning disabilities range from 30%-65%. Difficulties have been seen in all academic areas including word decoding (sounding out words), reading comprehension, math calculation, math problem solving, and spelling. We really see a lot of variability in the learning profiles of children with NF1.
2. I understand you’re doing a study on NF kids and their siblings, could you discuss that a bit further?
For our study, we recruit children with NF-1 and their siblings between the ages of three and six, and plan to follow them annually up until the age of 10 if possible. The goal of the study is to examine the cognitive and behavioral characteristics of NF-1 in young children to determine if we can see early signs of learning and attention problems. We are also hoping to learn more about the development of cognitive skills over time, and determine if this development differs from their siblings or other typically developing children.
3. What are some of the preliminary results you are finding?
We have found that learning and attention problems can in fact be identified in the preschool age range. There is no clear pattern to these difficulties. For example, some children have difficulty with verbal tasks (e.g., naming pictures, following directions), but do well on spatial tasks such as building with blocks. For other children, the opposite pattern is seen. Regardless of the pattern, most children with NF-1 have some difficulty in at least one area, although it may be mild. It is important that these difficulties can be identified at this young age because that allows interventions to be put in place earlier and prevents more pronounced learning and attention problems.
4. Discuss some of the medical drug studies that are being done.
Our research lab is not involved in medical drug studies, but please see http://www.ninds.nih.gov/disorders/neurofibromatosis/neurofibromatosis.htm for more information.
5. Have you found NF families having issues with the school in regards to learning issues?
The success that families have in getting services needed is variable based on the school system and the severity of difficulties the child has. NF-1 is associated with more mild difficulties compared to some other genetic disorders; however, children may qualify for an Individualized Education Program (IEP) under the Other Health Impairment category. This category is used when children have an identifiable medical condition (like NF-1), and have learning difficulties associated with the condition that require extra support in school. Children with NF-1 who are also diagnosed with ADHD may also qualify for a 504 plan. Generally, a 504 plan is used instead of an IEP when supports in the classroom alone (without additional special education supports like therapies) can help children succeed. Sometimes the learning or attention difficulties seen for children with NF-1 are a bit subtle. Parents may see them clearly, while schools see only mild differences from peers. In those cases, it can be challenging to show the school that the child needs extra supports.
6. Name some ways that parents can help their NF children who may have some learning issues.
Parents can help their children be successful by getting them a comprehensive assessment at an early age. These assessments are used to identify strengths and weaknesses so appropriate interventions can be put in place. This can help families get the services needed at school and direct parents about how to give their children extra practice with academic-related tasks at home. For example, if their children are having difficulty with early learning skills, it will be important for families to spend time playing rhyming games and reading together, and to talk about numbers and math-related concepts in everyday contexts. Parents can also help their children improve their attention and learn strategies to complete tasks by building up the amount of time their child can spend working in a structured setting.
7. Are parents reluctant to tell the teaching staff NF kids may have learning issues, if so why?
Some parents choose to not tell teaching staff about their child's NF-1 diagnosis to ensure that (s)he is not treated differently than other children. However, awareness of the diagnosis and the types of interventions that may help children with NF-1 is necessary if these children are going to get the services needed. We have found that most of the time, parents find it helpful for teachers to know that their child has NF-1.
8. Can NF kids also have attention issues such as ADD or ADHD in addition to any issues with NF, if so how often does this happen?
ADHD with or without hyperactivity is very common in the NF-1 population, with rates ranging from 30-60 %. For some, there are milder attention problems or organizational difficulties that don't reach the level for diagnosis, but nevertheless have some effect on the child's ability to do their best at school.
9. Name some of the behavioral issues that NF kids might have.
Given that attention problems are so common in NF-1, children with a diagnosis of both NF-1 and ADHD may be at risk for social difficulties. It will be important for parents to teach their children socials skills if any difficulties are noticed, and to give their children opportunities to practice these skills in social situations.
10. Explain the psychological issues that NF kids with learning issues have.
It is possible that children with NF-1 may experience anxiety or self-consciousness related to their physical symptoms and learning problems. There is not currently a lot of research looking at how common feelings of anxiety or withdrawal are in children with NF-1.
11. How and in what ways do the NF learning disorder differ and can they be confused for other disorders?
There is not yet enough research looking at whether the learning problems that children with NF-1 experience are very different from the learning problems of other children with learning disabilities but do not have NF-1. Learning problems in NF-1 are currently assessed in the same way that they would be for other children.
12. Explain some ways that NF kids with learning issues are helped. Are there special programs for them to help them succeed?
Children with NF-1 often have fine-motor difficulties and some have language difficulties. Depending on their pattern of strength and weakness, they may benefit from physical, occupational, and/or speech/language therapy services. Participation in extracurricular activities can give them opportunities to practice social skills. It may also be beneficial to attend NF-1 camps or find a local group to provide social support and show children with NF-1 that they are not alone. Local groups can be found at http://www.nfnetwork.org/
Thursday, February 9, 2012
Cancer Survivor Hollye Harrington Jacobs Shares Story

Since the time of my breast cancer diagnosis, we have talked openly with our five year-old daughter. While the personal nature of this circumstance made the conversations emotionally challenging, my professional experience as an adult and pediatric hospice nurse gave me both the tools and confidence to ensure that we gave her the developmentally appropriate answers.
Right after my treatment finished, our daughter has been revisiting a lot of the original questions as well as asking some new ones. For example, the other day while driving to school, Finally Five asked, “Do you think that your cancer will come back?” GULP.
So, I thought I’d take this opportunity to share with you her questions and our answers. These questions tend to be typical of most children affected by a cancer diagnosis.
- What is cancer?
- The body is made up of cells. Cells make our bodies work. They are so tiny that you need a microscope to see them.
- Cancer cells don’t look or act like normal cells. They don’t allow our normal, healthy cells to work properly. They can grow very fast and spread. Cancer cells may group together to form a tumor.
- There are many different types of cancer. Cancer can grow anywhere in the body.
- Finally Five wanted to know if a person could get cancer in your eyes, on your skin and in your legs.
- There is an iPad application called 3D4medical that has an image of a breast cancer cell. It is an ominous looking beast of a cell. This was really helpful for Finally Five to envision what was in my body and to then understand the sense of urgency (& drastic measures!) to get it out.
- Is cancer contagious?
- Cancer is not something that you can catch from someone else like you can a cold or the flu.
- You can be close to the person who has cancer and not worry about catching it.
- Did I cause cancer?
- No. Nothing that anyone does, says or thinks can cause cancer in someone else. Ever.
- Though they will rarely ask the question out loud, YES, children wonder whether they caused cancer. It’s sad, but true. If this question isn’t addressed, children can carry this fear (that they had some hand in causing cancer) with them into adulthood.
- Why do people get cancer?
- Most of the time, no one knows why someone gets cancer. It’s hard to not have all of the answers, but the truth is we don’t.
- What causes cancer?
- There is still a lot we don’t know about how cancer begins and what causes it?
- Sometimes cancer can be caused by some chemicals, air pollution (smoke), certain viruses and other things inside and outside the body.
- Do children get cancer?
- Yes, unfortunately children do get cancer. It is rare for children to get cancer. More adults get cancer than children.
- Who will take care of me?
- There are lots of people who will help me take care of you when I’m feeling sick. When I’m finished with my cancer treatment, I will be strong again. When I’m getting my treatment, I’ll be around as much as I possibly can and we will do different things when I’m sick, like watch Silver Lining movies and read books.Another reason to process information about cancer with parents is that children learn about cancer from other sources, e.g., school, television, the Internet, their classmates, and listening to other people talk. Some of this information is correct but a lot of it is not. Not knowing what is really going on or how to cope with information about cancer can be terrifying to a child.So, doesn’t it just make more sense to hear the information at home?Talking about cancer does not have to be traumatic. If anything, NOT talking about it is ultimately more traumatic. In the past, misplaced embarrassment about cancer has allowed misunderstandings and fears about the illness to grow. Remember: there are always professionals who are willing and able to help when parents feel overwhelmed by talking with children (Silver Lining). Engaging professional help when coping with cancer is a sign of strength and resourcefulness.Honesty is the first chapter of the book of wisdom.~Thomas Jefferson
- Go to the following sites to learn more about Hollye:
Monday, January 30, 2012
Interview with Rosie's mom

What are some words of advice that you have for other families who have children with NF?
Tuesday, December 13, 2011
Q & A with Catherine founder of Weelicious

Q1: Your website Weelicious, has become a go-to for easy, fast, nutritious meals and recipes for may families. What inspired you to get started on this cooking path?
A: I wanted to inspire my kids to be great eaters. I have always been fascinated how some children love good food--- why some are great eaters and some are picky. The idea of how much impact do you as a parent have on your children’s eating.
Q2: What do you love about cooking?
A: Beginning, middle and end. I love finding the produce at farmer’s markets that have fresh seasonal produce. I love cooking it and finally feeding my family.
Q3: What is the most popular dish people love from your website?
A: Oh so many-- Raspberry Cream Cheese Tart, Kale Chips, Cinnamon Roasted Chick Peas, Crock-pot Mexican Lasagna.
Q4: What is your all-time favorite recipe?
A: Parchment Fish. Cut pieces of parchment and your ready to go. You can throw in anything vegetables, fish, shrimp, tofu (for vegans), sauces and bake. It is great for a dinner party as everyone has a hand-in-creating what the are eating.
Q5: What is you son Kenya’s favorite hands-on dish to make?
A: Anything and everything. My children will eat anything when they help-out. Pick it at the farmer’s market or from a garden and chances sky rocket of them eating it. My son will actually say this pizza needs kale. Have them stuff the blender for smoothies. Really just get them involved.
Q6: Any tips on how we should stock the refrigerator and pantry?
A: Fruits in season, bananas, avocados, chicken, make pancakes or waffles and double, pasta rice beans, oatmeal, parmesan cheese.
Q7: Because we love green juice at the Littlest Tumor Foundation, what is a great smoothie you like for kids.
A: Get the kids to make. Super Juice-- kale, water, agave and lemon. It gives super-powers.
Q8: Daily recipe posts, weekly video clips, and much more on Weelicious. What is in the future for Weelicious?
A: Two books! One next summer --it will have 30% content of philosophy on how kids become great eaters. The second will be in 2013 a school lunch cookbook.
We at the Littlest Tumor Foundation cannot wait!
Thursday, December 8, 2011
Neurofibromatosis intern
My name is Mardy Wiesman, a recent spring 2011 graduate from University of Wisconsin-Oshkosh. I had gone to college for a journalism degree with an emphasis in advertising and religious studies minor. I enjoy writing and my dream job someday will to be a copywriter. I have recently started at the Littlest Tumor Foundation (LTF) in late November 2011. Here, I am going to be in charge of the blog and contacting fellow bloggers on the net to join the LTF blog.
Prior to my internship here, I had no idea what neurofibromatosis (NF) was at the time. I sometimes would watch The Learning Channel (TLC) from time to time and there were a handful of specials on the disorder from time to time, although I forgot the disorder’s name over the course of time. After reading the book “Understanding Neurofibromatosis: 2nd Edition An Introduction for Patients and Parents” by James Tonsgard, Ph.D., for LTF, I was able to connect the disorder with the documentary specials I had watched years before. One of the points of both the book and the documentaries was the mentioning of cafĂ©-au-lait or coffee mixed with milk-colored spots that were present on those who were afflicted with NF.
Then it came back to me. I remembered how some people would have these spots on their body and that would be all they would be afflicted with. Then I remembered how other people would get a more severe case of NF and have neurofibroma or tumors all over their bodies. Yet at the same time, NF is a common, yet relatively unheard of disorder. Here at LTF we are spreading the word on NF by means of social media such as blogging and Facebook, but also through events and campaigns. Together we can find a cure for children with NF before they reach adulthood. Join LTF today and soon we will find a treatment because, “Tumors in children, we do not like them!”
Wednesday, November 30, 2011
Neurofibromatosis and Green Juice
I was moved this week when I read an article written by my friend's sister. I wanted to use my blog this week to share it with you for two main reasons.
First, I wanted to give some publicity to the rare condition of Neurofibromatosis as it is something that many of us know nothing about. Briefly, it affects 1 in 3,000 children and causes tumors to grow anywhere in the body including the brain and spine and can cause a series of other significant health issues. They range from serious skeletal abnormalities, to endocrine issues, to difficult-to-treat cancers. Much is not understood.
Tracy Wirtanen, the author of the article I read, and my friend's sister, is the mother of an 8-year-old boy, Sami, who is diagnosed with Neurofibromatosis. You can read her blog here, where she wrote as a guest on Kriss Carr's website crazysexylife.com and you can find out more information about Neurofibromatosis at the website of the foundation she created at www.littlesttumorfoundation.com
Secondly, in her article, Tracy talks about the changes she and her family have chosen to make with regard to their nutrition, both for Sami and the other members of her family. She talks about the fact that Sami drinks green juice every day, and loves it, he even asks for it! I bring this up, because it highlights something that can get forgotten when we talk about juicing. This stuff is really good for you, at a cellular level. There is a real theraputic benefit in drinking vegetable and fruit juice. Our bodies can use the nutrients provided by the juice to both prevent future tumour growth, and help the body deal heal itself.
Yes, juice is a great vehicle to boost health and vitality, and help us to clean our systems when we have overindulged, but there is a more serious side to its benefits as well. If incorporating it into your diet will allow your body to battle cancer tumours, or give your body the tools it needs to prevent them developing in the first place, then what an incredible gift you can give to yourself, and your children every day! The gift of good health!
For those of you with juicers, then try the following Green Juice recipe, packed full of antioxidants, chlorophyll and good health.
Green Delight
3 kale stalks
1/4 pineapple (not peeled)
1 apple
1/2 piece ginger (not peeled)
1 stick celery
1/2 lime (not peeled)
Pack the kale into the juicer chute, and put the apple on top, then whizz every thing through the juicer. If you want to add some extra nutrients, then add a spoonful of spirulina to the juice and blend it with some ice.
Please do click on the link to both Tracy's article and her foundations website, she is doing terrific work to educate us about this potentially devastating disease.
If nothing else, give Tracy, Sami and her family a thought or a prayer over the coming weeks, and if you are lucky enough, be thankful for you and your families good health.
Happy Juicing,
Jx
http://millburn.patch.com/blog_posts/neurofibromatosis-and-green-juice