Comments on: Help for Chronic Lyme Disease Victims in Connecticut – Will It Stimulate Other States?

By: The Intensity of Lyme Disease Pain | About Lyme Disease

The Intensity of Lyme Disease Pain | About Lyme Disease — Mon, 28 Nov 2011 23:40:02 +0000

[...] Help for Chronic Lyme Disease Victims in Connecticut – Will It Stimulate Other States? [...]

By: Financial Aid for Testing Lyme Disease | About Lyme Disease

Financial Aid for Testing Lyme Disease | About Lyme Disease — Thu, 24 Nov 2011 13:49:10 +0000

[...] Help for Chronic Lyme Disease Victims in Connecticut – Will It Stimulate Other States? [...]

By: Social Security Disabilty for Lyme Disease | About Lyme Disease

Social Security Disabilty for Lyme Disease | About Lyme Disease — Sun, 20 Nov 2011 03:29:22 +0000

[...] Help for Chronic Lyme Disease Victims in Connecticut – Will It Stimulate Other States? [...]

By: New Treatment for Lingering Neuropathic Pain from Lyme Disease | About Lyme Disease

Wed, 02 Nov 2011 13:13:53 +0000

[...] Help for Chronic Lyme Disease Victims in Connecticut – Will It Stimulate Other States? [...]

By: NH Doctors can finally treat Lyme with long-term antibiotics legally | About Lyme Disease

Sun, 30 Oct 2011 14:52:20 +0000

[...] Help for Chronic Lyme Disease Victims in Connecticut – Will It Stimulate Other States? [...]

By: John

John — Thu, 23 Jul 2009 22:56:20 +0000

Hey Jenna i think i have rss feed on Dr. Frankenstein on my web site don’t remember doing it LOL but anyway i like your spirit we need to make as much noise as we can for all that we are going through with this Disease. I am most worried about the kids what about them and what future do they have with this awful Disease, we really need a break through so this war can end and we can get some research and some much needed relief.

http://www.ipetitions.com/petition/TheLymeShame/

By: Jenna Smith

Jenna Smith — Mon, 11 May 2009 18:01:43 +0000

Bob – I feel so very sympathetic to your despair, but don’t give up! There are docs who will treat your Lyme aggressively, you just have to hunt them down. Use the Federal programs that exist to help you with medical care, disability and medicine – just apply for the programs listing one of your disabling symptoms instead of Lyme. That is the key.

The cost for just my treatment – let alone a whole family – caused us to lose everything and now we are relying on the programs I mentioned to get by – so I feel your pain!

Don’t give up!

Blessings,
Jenna

By: Bob

Bob — Fri, 08 May 2009 16:50:22 +0000

It is very, very sad.

I have LD and my whole family has LD.

Spent tons of money, before being Diagnosed & still. Its to late for me & many of my family members. Most of us have chronic LD & Babisia.

Doctors Don’t beleive &/or care, are looking out for them selves.

I hope their will be a large Lawsuit against our goverment, etc. For not doing anything.