Guest guest Posted August 11, 2005 Report Share Posted August 11, 2005 Hi Beverly and all I have been writing letters since I was bitten in 1993. I know it is helping because there are lots of articles in the paper now. We need to keep it up. Each person that reads something is ONE more that may be educated or at least the light bulb may go on.............. hugs to all, Connie, Michigan Re: [ ] Re: disability (reply) > Thank you so much , I pray every night for all > of us with lyme that there will be a cure. The the > government will step up and to something, anything. > They will treat aids patients. (This is not intended > to put down anyone with aids, honest). But we are > just as ill. I have wrote to everyone of my State > reps, congresspeople, senators to tell them about Lyme > and that they need to LEARN something TRUE about it. > > God Bless you and your family. > > Love, > Beverly > > --- McGillycuddy <@...> wrote: > >> Beverly, >> >> I do sympathize with you. My family (wife and son) >> have Lyme and >> we're all trying to grasp why Lyme is such a big >> secret. The bottom >> line is money; the cost of long term antibiotics >> that the insurance >> companies would have to pay out. That's the >> pathetic reason why it >> is being kept such a big secret. >> >> My prayers will be with you and your family! >> >> Be well, >> >> >> >> >> > >> > > In a message dated 08/07/2005 1:52:47 AM US >> Mountain >> > > Standard Time, >> > > tnbarbsmom@y... writes: >> > > >> > > >> > > > Our income is so low and since i have >> > > > lost my Tenncare, no medical insurance and no >> > > pharmacy >> > > > insurance. I can't even get my meds. This >> scares >> > > me so >> > > > bad. I am going to send copies of all kinds >> of >> > > info >> > > > about lyme disease and what I can find about >> the >> > > co >> > > > infections (have not been tested for them >> though) >> > > > probably would be negative since fortunately I >> > > still >> > > > have a few doxy left. >> > > >> > > *******Beverly....I am putting together a >> project >> > > that perhaps I can help you >> > > with a solution for your meds. Send me a lists >> of >> > > the meds you are on and I >> > > will find the manufacturer for you and see if >> they >> > > have a " free " to the needy >> > > program. Since your income is low and you are >> > > without insurance, I assume you >> > > would qualify. This means thaat they send you 4 >> > > months of free meds at a >> > > time. >> > > You doctor files (fills out) the form and they >> mail >> > > the drugs to your doctor >> > > and the forms filed will last for one year. >> Most >> > > pharmaceutical companies >> > > have these programs. You can look them up >> > > yourself, or I just might already >> > > have the website and 800 number. I'm doing this >> for >> > > our " new " website. All your >> > > doc has to do it call at 3.5 months for your >> refill >> > > and they mail them out >> > > again. I'm assuming you have already files for >> SS >> > > disability? The good news is >> > > even if they take a couple of years for approval >> > > (God forbid) you will get >> > > back benefits from the day you filed.... >> > > >> > > Angel Huggzz >> > > or Angel >> > > >> > > Keep a smile on your face, love in your heart >> and >> > > walk with the angels, >> > > holding hands in the " chain of love " ..... >> > > >> > > Angel Huggzz >> > > or Angel >> > > >> > > L.E.A.P. Arizona, Inc.~~www.leaparizona.com >> <<<NEW >> > > http://leaparizona.com/ >> > > >> > > LYME Disease MESSAGE BOARD >> > > >> > >> > http://www.activeboard.com/forum.spark?forumID=31898 & >> > > sparkKey=5deb6043cb822f894a67a93a42ebc294b0 >> > > >> > > SUBSCRIBE TO: PhotonGenieElectromedicine (email >> > > group) >> > > >> > >> > PhotonGenieElectromedicine/ >> > > >> > > >> > > Hepheimers Hepatitis Hut General Boards >> > > >> > >> > http://www.activeboard.com/forum.spark?forumID=28120 & >> > > sparkKey=3bb629fe2d3efa7663cb48c41896c349b0 >> > === message truncated === > > > > > ____________________________________________________ > Start your day with - make it your home page > http://www./r/hs > > > > > Questions and/or comments can be directed to the list owner at > -Owner > > Quote Link to comment Share on other sites More sharing options...
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