LymeNet Flash: Anyone from CT know good support group?

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»	LymeNet Flash » Questions and Discussion » Medical Questions » Anyone from CT know good support group?

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Author

Topic: Anyone from CT know good support group?

humanbeing
LymeNet Contributor
Member # 8572

posted

So I need a support group to help me, I think.

My husband is getting tired of listening to me whine. My friend are creeping away.

I'm on costline of CT...looking for lymies who are whining together. [dizzy]

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We are spiritual beings on a human journey...

www.ruggierogallery.com

Posts: 906 | From CT | Registered: Jan 2006 | IP: Logged |

vitch
LymeNet Contributor
Member # 8094

posted

I PMed you.

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[email protected]

www.lymediseaseassociation.org/Conflicts.doc

Worthless tests & labs, a dangerous vaccine, insurance companies refuse to pay, undertreatment the norm, all about money. MO.

Posts: 281 | From CT | Registered: Oct 2005 | IP: Logged |

JustMeInCT
LymeNet Contributor
Member # 7237

posted

Where in Connecticut HumanBeing?

Posts: 122 | From Connecticut Shoreline | Registered: Apr 2005 | IP: Logged |

vitch
LymeNet Contributor
Member # 8094

posted

Chere took over Kathleen's support group and, last I knew, it was in Lyme/Old Lyme. I'm surprised it's not listed in the support groups on the left. It may not be in existance anymore.

--------------------
[email protected]

www.lymediseaseassociation.org/Conflicts.doc

Worthless tests & labs, a dangerous vaccine, insurance companies refuse to pay, undertreatment the norm, all about money. MO.

Posts: 281 | From CT | Registered: Oct 2005 | IP: Logged |

humanbeing
LymeNet Contributor
Member # 8572

posted

Thanks,
I will try Chere. Hope it is still there!

If others here are new to lyme (in the early stages of treatment)and from shoreline ct please pm me.

Thanks, [group hug]

Kim

--------------------
We are spiritual beings on a human journey...

www.ruggierogallery.com

Posts: 906 | From CT | Registered: Jan 2006 | IP: Logged |

pmerv
Frequent Contributor (1K+ posts)
Member # 1504

posted

You said you wanted other people to whine with. I'm not into whining that much, so I don't know about groups that whine, but if you want to do something constructive with your anger and discouragement, I know Time for Lyme does great work and would welcome more help. If you're interested, contact me and I'll give you some names and numbers.

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Phyllis Mervine
LymeDisease.org

Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001 | IP: Logged |

Andie333
Frequent Contributor (1K+ posts)
Member # 7370

posted

Human,

I know that early on in my treatment I was really confounded by the complicated nature of this disease -- how my feelings and symptoms shifted. I also felt overhelmed sometimes and depressed.

My SO was patient but that only stretches so far.

I found a therapist, made an appointment and set up twice-monthly appointments. Basically, I just needed to vent about my experiences and didn't feel I had the stamina to do any sort of volunteer type work.

Since my insurance covered the doc, it didn't cost much at all.

Hope this helps!

Andie

Posts: 2549 | From never never land | Registered: May 2005 | IP: Logged |

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