Back in November, Fox News 13 of Memphis, TN reported on a 3-year-old child that had exhausted her options in search of a treatment for her debilitating seizures. That is, except for one medicine that her family couldn’t get access to due to state and federal laws that block access to the medicine.
By age 3 Chloe had suffered from more than 75,000 seizures, affecting development of muscles, coordination, and cognition. Suffering from around 100 seizures per day, doctors tried everything in the book to heal young Chloe, including multiple surgeries at Le Bonheur Children’s Hospital and 20 different types of medication. In November her family reported that she was taking 5 medications 3 times a day including medications like Methadone. One of the medications forced Chloe’s parents to sign a waiver due to a severe risk of blindness as a side effect.
Back in January Chloe’s grandmother, Gail Grauer, went in front of state legislators to ask for access to the non-psychoactive form of cannabis oil. Legislators soon passed a bill allowing clinical research from Vanderbilt University in conjunction with Tennessee Tech to grow and distribute the medicine to sick children in need. However, Federal regulations blocked this course of action putting Chloe and her family in life-threatening bind.
In November, Chloe’s mother, Elizabeth Peden said, “You want to do anything, you would do anything, you would literally do anything to save the life of your child.” Her father Shea added, “One day we will be able to try it and we will be able to get those smiles and those little laughs that a lot of people to take for granted.” Tragically, that day never came for Chloe.
On December 10, Fox News Memphis reported that Gail Grauer died waiting for the treatment she so desperately needed. Sadly, many parents around the country could be facing this life-threatening scenario with their hands tied by the Federal government. In the United States alone, around 3 million individuals suffer from epilepsy.
At the Federal level traction is picking up, but children who are dying for a cure can’t wait for the slow and politicized legislative process to creep along. In July, Pennsylvania Representative Scott Perry introduced a bill that would allow legalize the non-psychoactive CBD oil at the national level. The bill, H.R.5226 – Charlotte’s Web Medical Hemp Act of 2014 has just begun to gain traction in Congress and will likely be subject to a vote in early 2015. So far there are a total of 38 cosponsors on the bill.
If you would like to take action you can find your district’s Representative here. Write your Congressional leaders and urge them to jump on board with the bill before another child’s life is shamelessly lost due to an inhumane and undignified Federal law.
via: Fox News 13