Showing posts with label advocacy. Show all posts
Showing posts with label advocacy. Show all posts

Tuesday, March 19, 2013

Follow Wellness at our new Blog!

Hello subscribers!

We are now moving our content over to our new blog found at littlesttumorfoundation.org/blog/. There you will find more on wellness, recipes, interviews and of course, more info on us, Littlest Tumor Foundation!
Thanks for the years of reading and thoughtful insights. See you at the new blog!


Saturday, February 16, 2013

LTF Gets Signatures in Oshkosh

This week, the staff and interns of LTF is asking for signatures in Oshkosh that will be sent to the politicians on capitol hill to keep funding NF research. Interns are finding support among Oshkosh residents. We raising awareness by interacting with students and informing them about the importance of the continued research by the Department of Defense (DOD) for people with NF. With every last signature on the letter, Oshkosh students are letting us know that "tumors in children, we do not like them." So far we have over 900 letters of support of NF research that we'll send to our senators and congress people! You + me = a cure!





Tuesday, February 5, 2013

DC Advocacy!



This week Tracy and Lilla are in Washington D.C lobbying for the NF cause. We want Washington to know about the issue of NF and its affects on and families. Both in the Fox Valley and worldwide, we at the Littlest Tumor Foundation will be advocating for the continued NF research by the government.

In the meantime, interns back in Appleton are working around the clock planning for upcoming events at the Foundation. Don’t forget on February 23, 2012, we will be holding our ski-a-little benefit and talking circle at the Bubolz Nature Reserve here in Appleton. In addition, we are preparing for the crossover from our old website to our new website. Stay tuned for more updates!

Thursday, December 20, 2012

A Little Gala Tomorrow!

Don't let the winter snow keep you in. Come out in your ugly sweater for a great night of food, friends, and more! Tomorrow is the big day when we will have a little gala hosted by Littlest Tumor Foundation at the Copper Rock Coffee House's party room on College Ave. Appleton, Wisconsin from 6 p.m. to 9 p.m. See you there!

Friday, October 26, 2012

NF Symposium by Kimberly Burton





On October 13, 2012, NF Midwest held its 21st annual symposium in Chicago. I was blessed enough to be in attendance with many NF families to hear three wonderful presenters, Dr. James Tonsgard, Dr. David Viskochil, and Dr. Tiffany Dell’aquila.  Each professional held true to his or her topic of the day and gave us hope that change in the field is about to happen.


Dr. Tonsgard started the day off with his talk on the Natural History of NF1.  In his presentation, he discussed his work on the NF database and how it has helped him see differences in complications in the disorder. In addition, he also discussed his treatment of NF patients and how he would like to see more aggressive treatments that he believes is based on chemotherapy.  He also discussed briefly genetics, which was a natural transition into the topic of Dr. Viskochil. 

Dr. Viskochil’s morning presentation was on genetic testing in NF1 and his afternoon presentation was on NF1 and bone health.  Both presentations were very interesting.  The morning presentation was very heavy-handed on genetics, but he was very successful in presenting the material in a manner that everyone could understand.  He explained how the NF mutation occurs and what happens, when it happens. By using cartoon illustrations, he made this complicated process easy to understand.  In both presentations, he made it very clear that NF is a spectrum disorder, meaning that one person’s symptoms will be different than the next.  However, like most disorders, there are commonalities that occur among most people diagnosed with NF. 

In the afternoon presentation he discussed leg bone bowing and the research occurring to help correct the false joints that can happen if and when the bone breaks.  He also touched on scoliosis and how it affects most people diagnosed with NF.  Dr. Viskochil briefly discussed learning disabilities in children with NF.  He stated that about 51% of children with NF have school problems, but only 34% receive special education services.  He did not explain in more detail the reasons behind this, but it proved to be a natural transition into the next presenter.

Dr. Dell’aquila is a clinical psychologist who specializes in executive functioning.  Her presentation emphasized on an individual’s ability to manage daily routines and setting goals.  It was very informative for anyone who may have executive functioning problems.  She gave many signs to look for and easy ways to work on correcting them.  Overall, she was very inspirational and gave very good tips as to how to keep on track and accomplish the goals you have in sight. 

This was a great event put on by NF Midwest, it was very informative and gave a lot of hope for the research being done and that will be done in the future.  I think in time we will see the world of NF being changed for the better, as researchers discover new modifiers and factors that affect NF.  It is something to be on the look out for in the months and years to come.  

Monday, September 3, 2012

A Little Goodbye



Three of our LTF interns are hanging up the purple and are going to spread the principles of hope, love and compassion to their next endeavors. Let’s learn a little more about what they did for the foundation.
Kim was part of our social work branch of LTF. She spread the message of LTF across the Fox Valley and beyond! Pierson spearheaded our web presence. Seneca spent countless, but very fruitful hours, helping coordinate many of our activities from April’s Kids-On-Chemo to our Sam-i-am race and finally our Family Wellness Retreat.
We wish them the best of luck in the future!