LymeNet Flash: Floridians send ur story to Pres. of Fla. Senate

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»	LymeNet Flash » Questions and Discussion » General Support » Floridians send ur story to Pres. of Fla. Senate

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Topic: Floridians send ur story to Pres. of Fla. Senate

vrtualchik
Member
Member # 27927

posted

I'm not really sure which is the correct forum for this post, but I really feel this a important opportunity for Florida Lyme patients so I am posting it to all of them to give it the best chance at being read. If I offend anyone by placing it here I apologize.

Below is the information from an email that was sent to me by Dolores Claesson, a lyme advocate, who met this past Saturday with Mike Haridopolos the President of the Florida Senate. She asked that we pass this along to all Florida Lyme patients.
Here it is:

Please e-mail or call and tell your story to Mike Haridopolos, President of the FL Senate. His wife by the way is a physician and we need to get her involved. I talked with him about lyme disease in the State of FL and we need to get him to enact legislation to allow our physicians to treat long term for lyme. Same legislation as CT and many other states are enacting....He needs to know how this has affected Floridians, native born and naturalized !! The Squeaky wheel gets the grease. His assistant also gave me his contact info and we need to let them know what is happening in FL...

We need to ensure that the people of FL will also get treatment paid for by insurance companies, Medicare, Medicaid, Medicaid needy share a cost, Kids care or any other company operating within our State.

OK HERE IT IS NOW USE IT !!! [email protected] and he is on facebook www.facebook.com/SenatorMike or twitter at www.twitter.com/MikeHaridopolos or on the web at www.SenatorMike.com. His associate is Toby Philpot who is a GATOR by the way....and can be reached at 352-318-2008 or [email protected]. There are so many of us, and we have not connected so we do not know exactly how many there are...tell them your story...

Hugs to all, Dolores

I hope you all will take part. It'd be nice to have someone with political clout fighting on our behalf.

Posts: 86 | From Fort Lauderdale, Florida | Registered: Sep 2010 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

I can move it if you want me to. It may get more action in Activism.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001 | IP: Logged |

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