It is at the request of an awesome brother and quarterback for the Denver Bronchos, Tim Tebow, that I bring to you the story of a courageous young lady named Presli Collins and ask for your prayers. In 2008, This beautiful 9 year old little girl was diagnosed with a crippling condition known as NF1 or Neurofibromas. For those of you who are unfamiliar with NF1, CTF.org (Children’s Tumor Foundation) defines it as :
Neurofibromas, the most common tumors in NF, are benign growths which typically develop on or just underneath the surface of the skin but may also occur in deeper areas of the body. Neurofibromas, which are composed of tissue from the nervous system (neuro) and fibrous tissue (fibroma), usually develop around puberty although they may appear at any age. The tumors are not contagious. Nodule-like surface tumors are known as dermal neurofibromas. Plexiform neurofibromas grow diffusely under the skin surface or in deeper areas of the body.
The presence of multiple neurofibromas is an important diagnostic sign of NF. Single neurofibromas may occasionally occur in people who do not have NF. The number of neurofibromas varies widely among affected individuals from only a few to thousands. There is no way at present to predict how many neurofibromas a person will develop. Dermal neurofibromas rarely, if ever, become cancerous. Such a change, called a malignant transformation, may occur, although very rarely, in plexiform tumors. Therefore, it is important that patients be in the care of an NF specialist. Some neurofibromas, depending on their location and size, can be removed surgically if they become painful or infected, or cosmetically troublesome. A new tumor sometimes appears where one has been removed, particularly if that tumor was not removed completely. There is no evidence that removal of growths will increase the rate of appearance of new growths, or can cause incompletely removed tumors to change from benign to cancerous…
This is just a little about what this young lady has to deal with on a daily basis, but she is dealing with it like a champion. If you go to CTF.org you can read more about this disease and learn about ways you can spread the word and how to help. The symptoms and the complications alone from this disease is enough to make a grown man weep. Little Miss Collins has a facebook page that brother Tebow has asked for everyone to join to show your support, prayers, and love with this awesome young lady. Her Facebook profile is http://www.facebook.com/prayforpresli . If you would like to send letters of support or any other correspondence, you can send them to: Presli Collins, 1312 17th St. #116, Denver, CO, 80202.
Please show your love and support for Presli and her family as they deal with this life-altering illness. God bless you all. -Mike
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