The doctors I would like to thank and I am very grateful for are the ones that get up in the middle of the night to save lives in the operating room and spend six to eight hours doing so. What kind of super humans are these wonderful people who save lives by performing miracles? Their dedication is incredible.
I of course would like to thank all Lyme doctors as well and naturopaths acupuncturists and chiropractors and all dedicated doctors who help the sick and ill. YOU GUYS AMAZE ME AT TIMES!
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sutherngrl
Frequent Contributor (1K+ posts)
Member # 16270
posted
Thank you with all my heart to my wonderful LLMD. Thank you for all you do to help those who suffer with Lyme Disease. You are my hero and an angel.
Posts: 4035 | From Mississippi | Registered: Jul 2008
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'Kete-tracker
Frequent Contributor (1K+ posts)
Member # 17189
posted
Thanx 2 my LLND, in Portsmouth who I occ. follow up with. He ALSO deals w/ left-over neuro Lyme symptoms. (Dxed '02? On an ever-changing supplemental protocol. He looks as good as... I hope to eventually feel. )
Posts: 1233 | From Dover, NH | Registered: Sep 2008
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posted
Let me add my thanks to the LLMDs in our community. I am hearing great reports through PMs that so many patients are getting their lives back. It is amazing how things are turning around in my household!
THANK YOU LLMDs!!!! Posts: 170 | From New Jersey | Registered: Jun 2008
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bettyg
Unregistered
posted
TadichGrill,
for a newbie, what an outstanding way to start off posting .... things we take for granted!!
yes, i too am thankful for all our chronic LLMDS who practice ILADS guidelines; who have to fight to keep their medical licenses like:
Dr. Charles Jones, kids no. 1 llmd ... 3rd yr. of hearings by conn. health board,
Dr. Burrascano who stopped seeing lyme patients to do lyme research after he was hasseled!
Dr. Jemsek, NC, who had to move to SC, and start over losing his AIDS patients after building a new building for aids/lyme patients!
these are only a few of the handful of llmds i know who have had to FIGHT TO KEEP THEIR MEDICAL LICENSES in their states!
this is one time we can name llmds since they had charges filed against them!
What i love hearing most are the thank yous back to me for giving them names of our nationwide llmds in their states or their neighboring states.
it's a PERFECT MATCH; they are getting the help and personalities match too .... complete TEAMWORK !!
so to all llmds; THANK YOU for giving your lives so that we may get into remission and the few to be completely cured of lyme/co-infections! god bless each one of you!
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posted
Thank You LLMD's for helping the sickest of sick and the not so sick get so much better! You guys put your lives on the line for us and I personally can't thank you enough!
I hope some of the ducks see this as well so they can see these LLMD's care and are getting us better! Maybe someday they'll stop harrasing them and let them do what the do best!
posted
In addition to my wonderful LLMD, I'm very thankful to my PCP who is willing to work with my LLMD and help implement his treatment protocols! Just wish all PCP's would be as open-minded and compassionate.
-------------------- My comments on this site are not intended to be taken as medical advice as I'm not a physician. Posts: 206 | From Georgia | Registered: Dec 2008
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Starfall1969
Frequent Contributor (1K+ posts)
Member # 17353
posted
Yes, thank you to those doctors who help those of us who have any kind of hard to diagnose disease.
I am certain there has to be a place in heaven for LLMDs and others like them who take the time to CARE about the sickest of the sick!
God bless you all!
Posts: 1682 | From Dillsburg, PA | Registered: Sep 2008
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METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628
posted
Ugagal, did I end up getting the information on your PCP?
-------------------- I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.
I don't think I ever sent the info to you....I will send you a PM. Thanks for the reminder.
-------------------- My comments on this site are not intended to be taken as medical advice as I'm not a physician. Posts: 206 | From Georgia | Registered: Dec 2008
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Lyme police here, please delete LAST NAME of LLMD's.
betty???
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96220 | From Texas | Registered: Feb 2001
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Dekrator48
Frequent Contributor (5K+ posts)
Member # 18239
posted
A grateful thank you to my wonderful LLMD and his nurse (his wife), who tirelessly help many lyme patients.
Huge thanks to all the LLMD's who put themselves on the line everyday because they are courageous and want to do what is right.
Saying a prayer for all of them....
-------------------- The fibromyalgia I've had for 32 years was an undiagnosed Lyme symptom.
"For I know the plans I have for you", declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future". -Jeremiah 29:11 Posts: 6076 | From Pennsylvania, USA | Registered: Nov 2008
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seekhelp
Frequent Contributor (5K+ posts)
Member # 15067
posted
I have no doctors to thank outside of LLMDs. Everyone left me for dead.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
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bettyg
Unregistered
posted
peggy,
all 3 have had charges against them so their names are public which was explained to me long ago from the old-timers here. confusing i know.
dr. burrascano retired; so he's no longer active.
peggy, i do see your point otherwise.
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posted
Thank you Thank You to my LLMD who clinically diagnosed me and has saved me from the dreaded path of doctors who couldn't. I am lucky that I only went to 2 primary care physicians and one neurologist before my LLMD.
I would like to thank one primary for thinking enough to test me, but thats about all. Another primary for encouraging me to do whatever I had to to feel better even though he couldn't do anything else for me. He even suggested a holistic route.
And I would like to thank my friend who is a trauma nurse who wants to learn from me. Asks questions and listens so maybe she can help one day.
Posts: 193 | From New Jersey | Registered: Oct 2008
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I still don't understand why you think it's OK to post their last names. I've been a member of Lymenet for 8 years and I haven't heard this before. Has the policy changed?
5. You also agree not to post the last name, or the first name, of any person that treats Lyme disease. Instead, please use the first initial of the last name only, with the state, but not city. For example, Dr. B. in NY. This person's contact information should not be displayed on LymeNet. However, you may email this information. This is to protect those that treat Lyme and the Lyme community.
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/