Some states fund homeless veteran housing, in various forms--never the VA. Sometimes it's a kinda scuzzy day shelter, meaning you can sleep and eat there but have to leave in the mornings. Sometimes it's a place more like a boarding house. I live at one of these: you pay a third of your income and get a roommate, or $400 a month for a room to yourself. These are not The Hilton.
Often the state (not the VA) then looks for a GOOD social worker on site, to help find services; and for a GOOD nurse on site and a GOOD job finder person on site. Not lousy VA services. Meals may be free, using food from the local food bank. Perhaps you may use their social services or get free on-site meals, even though you don't live there. Be bold--ask!
I am termed "homeless veteran" but I have a roof over my head--in fact, my own room, for which I am grateful.
For the location of a facility, the VA almost never tells seriously ill patients. Instead, try calling a public day shelter for drunks / hard drug users (not a place for a sick Lyme patient--very dangerous and they may not have a frig for meds, nor a secure location for expensive meds and often Home Healthcare nurses won't go near those places.) Call because they may know of a place for veterans in your area. If not, ask about the surrounding cities or states.
Or ask your democratic congressperson's local office people.
Veterans can go to: http://www.nchv.org/ (National Coalition For Homeless Veterans.)At that site, on the left, click and hold the "homeless" reference, then click "providers." You may find clues. Some places on there don't exist, never have. With others you may not be able to tell if it's a live-in place.
Please spread the word. And there are hundreds of thousands of we female vets, too!
Please tell veterans of Iraq and Afghanistan. They are probably the most ill treated of all veterans, by the VA.
By the way, the VA refuses to properly diagnose and to properly treat chronic Lyme disease patients. That is their nationwide, unwritten policy.
Service-connected contraction of Lyme disease may be possible, but you have to fight! Search for Military Lyme Support at Yahoo, or try health.groups.yahoo.com/group/militarylyme/
Here is [URL=http://www.streetsthatspeak.com,][/URL] a public forum for those homeless or going homeless.
thank you for sharing your expertise in this area as well! i think you covered all 3 major areas you wrote to me about privately.
this will help generate more discussion and other tips, etc. to help the veterans, lyme patients, etc.
i'll find out more about iowa's natl. guard employees about lyme disease as i was told in june or july that IOWA WAS NOW PAYING BILLS OR LYME PTIENTS WHO ARE GUARD MEMBERS!
IP: Logged |
minoucat
Frequent Contributor (1K+ posts)
Member # 5175
posted
Daise, thank you so much for posting this. You speak for people we often don't hear from and tend to forget. I hope we hear more from you.
I've added your info to my Disablity thread.
I'm so very glad you've found this site. It's dreadful that the most vulnerable and needy amongst us have the least access to the internet, and to information, medical care, and help in general.
There are many people in our LD group who don't have the gas money to attend meetings, who are not online, and who can afford only limited time on their phones. And those are the ones I know about -- it makes me ill to think of the people who are falling entirely through the cracks.
-------------------- ********************* RECIDITE, PLEBES! Gero rem imperialem! (Stand aside plebians! I am on imperial business.)
oops; slip of the tongue; send off meaning RETIREMENT!
i wasn't able to make it down that day; couldn't find a ride with my other brothers! with the high volume traffic, i didn't want to drive alone.
so didn't get a chance to talk to the higher ups as i planned on doing about their lyme/tick policies!
if i get a chance, i'll try to ask at xmas time, since 2 will be there; 1 retiree and 1 still working! they are so secretitive; so don't hold your breath!
IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/