ABRAM MAYHEM
  • Home
    • About Abe >
      • Abram’s Viral Photo: The Wizard of Awws (Baby Ming) | Abram Mayhem
  • Blog
  • In the News
  • UBE2A Deficiency Syndrome
    • UBE2A Publication List
    • Abram's UBE2A Symptoms and Diagnoses >
      • Abram’s Pineal Cyst Journey: Insights, Updates, and Long-Term Care >
        • MRI Imaging of Pineal Cysts in UBE2A Deficiency
    • Why Genetic Testing
  • Helpful Links
  • Abram's Art

Reaching out to Iowa's Senators for Abe...

1/18/2016

Comments

 
Picture
 I think many of you can recall the mad dash I was making last spring and summer to be able to obtain CBD legally for my son, Abram. After having very scary and serious side effects on the pharmaceutical drugs Keppra and Klonopin, we had decided to pursue CBD as an option (at the urging of our Neurologist) however due to Unity Point's stance on CBD - he was unable to help us get the Cannabidiol Registration Card.

At that point, I began my fight: both for my child's health care and diagnosis and for his personal freedoms to try cannabis as a treatment option. I wrote to every single Republican Senator as well as every single Representative in the Republican House (but that's another post entirely).

I must be honest in saying that as a mother trying to fight for her child's rights - it is very disheartening to say that out of 24 Iowa Senators - only 5 have ever responded to my concerns and questions regarding my son's healthcare and his rights as an Iowan and an American. As a parent with a special needs child, I should be spending my son's nap time as my own down time but instead I sit in front of this computer tapping away on the keys begging for anyone and everyone to LISTEN. 

When I began writing to the Senators and House Members, as a mother sharing Abram's story - my son's story has changed immensely. First, he was a little boy needing legal access to CBD and I was begging for help since our city's own Children's Hospital was not helping us gain legality. Now he is a child who is TWO HUNDRED AND FIVE DAYS SEIZURE FREE and I am a mother who finally holds a Cannabidiol Registration Card in her hands today. However, they need to realize that in order to get the card, my son had to endure another MRI, a spinal tap, numerous meetings with geneticists, genetic researchers and medical researchers who were trying to help us. My son finally has a diagnosis that is incredibly rare and the only other family world-wide who shares this same mutation lost a child at age 11 to an epileptic seizure. These facts make me worry, make me squirm and make me realize even more WE NEED ACCESS NOW.

So here I am, over 100 e-mails deep just to our Iowa Senators to which only five of whom responded to my concerns. My issue with writing to our state senators is this: If you have a health issue like my son's - they don't want to hear about it unless you are in their district. I hear time and time again that I need to contact my own Representative (I already have) and to contact my own Senator (he's been to our home and met my family in person).  

Health concerns of a toddler is not a "district issue". It is an Iowan issue. It is an American issue. It is also a world-wide issue and phenomenon that we are dealing with. Once again, my zip code should NOT dictate if my son's story is worth responding to.

I have a friend whose child suffers similar issues to Abram and her family was DENIED access to the Cannabidiol Registration Card because her Neurologist resides at a Level 4 Epilepsy Unit out-of-state. So, despite the fact that he is the best-of-the-best in the country and supports the use of cannabidiol, that physician is not counted due to the fact that he is not an Iowan Neurologist. How is that fair? When you have a child who has rare diagnoses like many of Iowa's most fragile constituents, you are also going to be punished for being forced to get care out-of-state because our own hospitals aren't equipped or are unwilling to help our children?

My son is 205 Days Seizure Free. (My son was healed illegally for 163 of them.)

I am not a criminal. Please quit making parents choose between being lawful and being a good and present parent. Most importantly, please, take the time to respond to the parents of suffering children in your state. Please stop making children wait. We need action from you.

Many thanks to Senator Brad Zaun, Senator Charles Schneider, Senator Jake Chapman, Senator Tim Kraayenbrink and Senator Michael Breitbach for taking the time to respond to my concerns. Your time and attention to this matter is greatly appreciated.

Sincerely, 
Abram's Mom

Comments
    Picture

    About Me

    Erin is a green-haired, tattoo-covered mama powered by sarcasm, iced coffee, and the occasional emotional spiral.

    She’s raising an incredible son with a rare genetic condition, advocating with sharp knowledge and a softer heart — because both matter.

    She's trying not to lose her mind in a house that includes her husband, her son, her mother, a team of no less than five workers, and approximately 3,000 daily interruptions.

    She’s got a sixth sense for fake people, a deep love for horror movies, and a soft spot for anyone who’s ever felt like too much and not enough at the same time.

    Erin doesn’t pretend life is perfect. She shows up messy, honest, and real—whether she’s in advocacy mode, snack-fetching mode, or “why is everything a mess” mode.

    ​She’s built of grit, wit, compassion, and just enough rage to get things done.​


    MOST POPULAR BlOG ENTRY

    Picture
    The Isolation
    ​of Special Needs Parenting

      Subscribe!

    Subscribe to Blog

    JOIN US
    ON SOCIAL MEDIA!

    Picture
    Picture

    Archives

    June 2025
    February 2025
    December 2024
    November 2024
    October 2024
    September 2024
    July 2024
    March 2024
    January 2023
    May 2020
    December 2019
    March 2019
    January 2019
    November 2018
    September 2018
    July 2018
    May 2018
    March 2018
    February 2018
    January 2018
    December 2017
    October 2017
    September 2017
    July 2017
    June 2017
    May 2017
    April 2017
    March 2017
    February 2017
    January 2017
    December 2016
    November 2016
    October 2016
    September 2016
    August 2016
    July 2016
    June 2016
    May 2016
    April 2016
    March 2016
    February 2016
    January 2016
    December 2015
    November 2015
    October 2015
    September 2015
    August 2015
    July 2015
    June 2015
    May 2015
    April 2015
    March 2015
    November 2014
    October 2014
    July 2014
    May 2014
    April 2014
    February 2014
    January 2014
    December 2013
    November 2013
    October 2013
    September 2013
    August 2013
    July 2013

    RSS Feed

Proudly powered by Weebly
  • Home
    • About Abe >
      • Abram’s Viral Photo: The Wizard of Awws (Baby Ming) | Abram Mayhem
  • Blog
  • In the News
  • UBE2A Deficiency Syndrome
    • UBE2A Publication List
    • Abram's UBE2A Symptoms and Diagnoses >
      • Abram’s Pineal Cyst Journey: Insights, Updates, and Long-Term Care >
        • MRI Imaging of Pineal Cysts in UBE2A Deficiency
    • Why Genetic Testing
  • Helpful Links
  • Abram's Art

© 2024 Abram Mayhem's Journey. All Rights Reserved.

Stay connected with us on our website or follow our blog for the latest updates on Abram’s journey with UBE2A Deficiency Syndrome and advocacy efforts.

Facebook | Instagram | Twitter