AI summary & topic connections
Describes personal and children's symptoms attributed to wireless exposure, restricted travel and costly mitigation, and requests prompt regulation and support.
- Children & vulnerable groups: “d than done especially when I'm dealing with 2 special needs kids at home who need services. Both of my special needs kids struggl”
- Towers & siting: “y making the correlation of my symptoms with cell phone towers and boosters cities have put up. I noticed every time I drove through certain”
- Neurological symptoms & sleep: “oint she can't stand, she has to sit and her dizzy spells leave her crying on the floor. She too also gets really depresse”
- Housing, work & access barriers: “re too high like her brother. We have had to spend so much money trying different devices and clothing that claims to repel EMF's”
- Exposure limits & oversight: “ened bodies. We have no help, no support and nothing is regulated which HAS to change and not years from now, TODAY, PLEASE!!!”
ORIGINAL COMMENT · UNEDITED TEXT
I am submitting this comment in response to HHS’s Request for Information on Electromagnetic Fields (EMFs), Radiofrequency (RF) Radiation, and Wireless Radiation Exposure.
I am responding from the perspective of my own experience as well as 2 of my children. For myself I suffered for almost 4 years before finally making the correlation of my symptoms with cell phone towers and boosters cities have put up. I noticed every time I drove through certain areas of our city I'd get what felt like an electric jolt go through my arms and I'd be left with relentless fatigue. I now have to avoid areas of my city where cell signals are boosted as my body immediately feels the unpleasant jolts. I live in constant paranoia driving around town and especially to other cities knowing I may get these electric jolts going through my arms and then left with horrible fatigue. Doctors do not know what to do with me, I was told by one physician to "just move out to the country" which is easier said than done especially when I'm dealing with 2 special needs kids at home who need services. Both of my special needs kids struggle with EMF's, it's very clear when they have had way too much exposure via at school, malls, city parks w/cell towers etc... My son gets extremely agitated very easily and becomes self-injurious as well as depressed. When my daughter is exposed to everyday EMF exposures her POTS/MCAS and Ehlers-Danlos all collide into a nightmare. She sweats horribly, she is overly stimulated and can't get her words out her energy goes way down to the point she can't stand, she has to sit and her dizzy spells leave her crying on the floor. She too also gets really depressed when EMF's are too high like her brother. We have had to spend so much money trying different devices and clothing that claims to repel EMF's but when it's a constant bombardment life is never enjoyable, we are just trying to survive each day. I am fearful for 6G being rolled out as I fear its may land one of my children in the hospital which is riddled with EMF's and what that could do to either of them and their already weakened bodies. We have no help, no support and nothing is regulated which HAS to change and not years from now, TODAY, PLEASE!!!
Discussion
Reader replies are separate from the official HHS submission. They are reviewed before publication. Display names are not verified.