Comment from Murphy Diane
AnonymousOpposeIndividual
Summary: Diane Murphy, a patient with a thyroid condition, opposes the FDA's reclassification of desiccated thyroid extract (DTE) as a biologic. She argues that this change creates unnecessary barriers to access, threatens the role of compounding pharmacies, and will lead to higher costs and fewer treatment options for patients who rely on DTE.
Docket No. FDA-2015-D-4750-0439
Food and Drug Administration
5630 Fishers Lane, Room 1061
Rockville, MD 20852
Please do not let my access to natural desiccated thyroid hormone to be taken away from me. As a patient who no longer has a thyroid for 21 years I need to have all the hormones T4, T3, T2 , T1 to be a fully functional member of society and to continue to work and provide for myself and help my aging family members. Natural desiccated thyroid hormone has been prescribed to me by my doctor as it has the best medical outcomes for me. I also have DIO1 & DIO2 gene mutations that make it nearly impossible for my other organs to convert inactive T4 into active T3 thyroid hormone.
I cannot function well without it - natural desiccated thyroid hormone relieves severe brain fog, (possibly dementia overtime) , and improves all my metabolic outcomes and greatly improves my eye health and vision.
Thank you , Diane Murphy
Re: FDA’s Reclassification of Desiccated Thyroid Extract (DTE) as a Biologic
To Whom It May Concern:
I am writing with deep concern about the FDA’s recent decision to reclassify desiccated thyroid extract (DTE) as a biologic. For more than 100 years, DTE has been a lifeline for patients like me who do not do well on synthetic thyroid medicines. The decision puts that lifeline at risk.
For many of us, DTE isn’t just another treatment option, it’s the only treatment that makes daily life possible. Without it, we face fatigue, weight gain, brain fog, depression, and countless other symptoms that make even basic tasks difficult. I have seen how quickly quality of life deteriorates when DTE is taken away, and I am not alone.
This reclassification just doesn’t make sense for patients. It creates unnecessary barriers and opens the door for a single company to control the product, driving up costs and shutting out the compounding pharmacies that have provided access to this medicine for years. The result will be fewer choices, higher prices, and patients left with no effective alternatives.
I urge the FDA to reconsider this harmful action. Please keep DTE regulated the same way it has been for decades, protect patient choice and access, and put patients first by ensuring DTE remains available at compounding pharmacies for when other treatments fail.
For hundreds and thousands of Americans, this is not an abstract policy change. It’s about whether we can live full, healthy lives. I ask you to stand with patients and preserve access to DTE.
Respectfully, Diane Murphy