Mail bullieing to EMF sensitives

I have been receiving mail bullying from a local service agency due to my need to avoid exposure.  The letter is the same handwriting and same postal code and stamp as other things they sent, hence I know it's them.  Someone also told me they are the ones doing lots of backstabbing and trying to get me denied for needed services due to my condition.  The last thing they mailed me was a print out of the "scathing" wikpedia page that so many ES complain of and is grossly out of date.

What I received link here:  https://en.wikipedia.org/wiki/Electromagnetic_hypersensitivity

I do know the local ADA law center will not help as they feel as the "mail bullies" do.

I am ignring it for now. But really I should not be putting up w/ this kind of behavior from anyone:

I still require this agencies services or I will not have food on my table. But they are trying to cut me from their services as theydo not want to service a crazy person that claims wireleless makes them sick.

Any Ideas???

Would love feedback

Also note:  I have bookmarked and also saved to my computer the 2 previous posts of Dr's statements and Dr's sworn testimony our own Fog Top recently posted and may have someone forward those to the agency.

That is so bizarre and really disturbing.  I don't know how legally "feelings" about denying electrosensitives their human rights can fly.  The leading expert on EHS, Olle Johansson, has secured recognition of EHS as a functional impairment in an internationally applicable classification, so the justice department is obligated to administer ADA for electrohypersensitive citizens.  Are you saying this bullying is from a private organization trying to stop you from getting momentum in advocacy that would spread to others who are EHS? I'm sorry I'm not getting the picture.

The mail bullies are a private volunteer organization that shops for old/disabled shut in's-I have many other conditions besides ES that make me qualify, but due to the ES they have been looking for any excuse to dump me from their services.  I have to say this place has sent some wonderful volunteers and I am so grateful for their services and I need them so bad.  The latest volunteer assigned me and also my old case worker confided that they have issues w/ the ES and do not want to service a "crazy".  Tried to go to the social worker a month ago, but she is no longer there.  The current volunteer that is now doing my shipping has a science/logic background and understands what RF radiation can do to the body.  

The ADA law center, have tried to get them to work w/ me as I need access to  certain public services that are loaded w/ wifi and accommodation in other areas to not be forced exposure.  Both times they came back saying they will not help me as ES is not a condition they will work with.  I have found that in AZ there is big movement for all public/private agencies to refuse services as much as they can to the disabled-big scam that is so cleverly fixed-from the top officials down to the local offices. I have gotten court rulings in my favor or other things like food stamps, but they will not enforce.

Yes I would think that sending things like that through the mail would be highly illegal-as it's just nasty, but then if I complain, I may find that my packages will start being delivered to the bottom of a trash can again.  I finally got the carriers to stop listening to the landlord's badmouthing and see me for a person. Yes he is badmouthing me to again for being crazy, as he claims things that bother me put out "nothing".  The volunteer that is shopping for me now claims that he measured it  and saw the inside of the thing and it's not nothing.

I have just ignored it, as not to loose much needed and required services I do have, but yes I find this "mail bullying" extreme. As I am sure most here have previously read and been quite offended by that wikpedia article they sent.  I have seen post on that going way back.

Thinking of seeing if the guy shopping for me now will present those 2 documents by top MD's that fog top posted here earlier in other posts-by far the best testimonials I have seen!  I worry about making waves, as people are pretty set in their views about ES and no one can tell them different.  

At least in NM some will accommodate ES as it's considered a major mental condition and they must do so for those.  Here they do not.   Hope this helps explain. So getting advocacy and the other organization's services are very separate issues.  It would help much if I could get advocacy and would put a stop to the problem and many others I must face day to day.