MAN, I COULD GO ON FOREVER!
Now do you want to know about his staff?
DITTO
So good of you lymetoo to help your neighbor!
You are one in a million!
Love,
Janie
He sides with your spouse and picks on you..oh wait..that's not the kind of stuff you wanted to hear. Hahhaa.
Nothing is to 'weird' to tell him. I think he's only laughed at me once!
Hahaha.
I think he's the greatest. I've never met a doctor like him...here or when I lived in Canada.
DT
I went to Dr. C on a very strong recommendation my hero, just don! I had a lenghtly talk one evening with him. Dr. C should be giving him commissions!
I cannot wait until he sees this post, he will fill it up for us, so I have to get my words in so he does not "rain on my parade"!
The knowledge this man carries in incredible! His honesty about the disease is one I had never heard from any of the other doctors I had seen. He is a man with much integrity.
He thinks he has heard it all until you come with another symptom. I told him when I was so sick, even my finger nails hurt! He laughed, said that was a "new" one, wrote it down and shook his head! It was a great moment and......did not doubt me! (they really did not hurt!)
You can call anytime with questions or problems. He always answers the questions with the concern that a doctor should have. I have gotten my answers promptly, I did not wait for 3 days for a call back!
He believes in you! More than I can say for the other 30 ducks that I seen. He doubts nothing. He even told me that some of the things I have told him do not make sense on paper, but.......he has had other patients tell him the same thing......he believes it, he said with this disease, anything is possible!
The encouragement he gives is incredible! His excitment is overwhelming! I had a phone consultation with him 2 weeks ago. He was so excited about the progress I had made, he was more excited than I was! I guess I made more progress than I thought!
He is excited about you. He is concerned for your health. He is concerned for you.
In closing of this long post, the one thing that has stuck out in my mind was a statement he made to me the first time we met.
"I will not promise I can cure you, but I will give it my best shot. I know you have seen 31 other doctors with this disease. I am number 32 and I will be the last."
He restored my self confidence and gave me a new lease on life!
Janell
Ok..I remember again!
Hahhaha!
My duck *cough cough* told me that he had actually been in Doctor school with our good Dr. He also said that if there's a chance to beat LD, then I have the right doc looking after me. He told me that our Doc was the first physician in Missouri to ever diagnos LD. However, our Doc does not remember my duck.
Hahhaha
(First impression mean a lot, ha!)
DT
quote:
Originally posted by dt:
..... He also said that if there's a chance to beat LD, then I have the right doc looking after me. He told me that our Doc was the first physician in Missouri to ever diagnos LD.
WOW, dt!! That's awesome!!
DT
Did ya see the post by daybyday on medical!
Dr. C. is reachin out to help another doc become LL and to help this doc's family!
I am so proud of our GREAT doc. HOORAY!
And Sheila yes you will get better!
Take care,
Janie
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Lymetutu
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I really like the idea that he allows those of us who are really far from him to work with our local doctors on getting our blood
work done.
The fact that he doesn't insist on return visits every month or so, really helps those
of us who can't travel that far that often.
That shows to me he is more concerned about
the patient getting treatment than the dollars in his pocket.
Now that's refreshing.
Really, I enjoyed my visit with him and his handouts are the best explainations.
By him allowing us "distant patients" to work locally with our reg PCP's (if we have one who is understanding), then he is giving
a chance that more reg docs will recognize
LD with future patients with it and thereby
educating more doc about this disease and
how hard it is to treat.
Thanks Dr. C in Missouri!!!!!!
I agree with everything posted....
works to educate all other non-literate doctors he can.
Wonderful, wonderful man.
Trout Scout 
[This message has been edited by troutscout (edited 30 October 2002).]
[This message has been edited by momtoeight (edited 30 October 2002).]
Well, in addition of what I said in an earlier post, I get to go on a little vacation at least twice a year! The best part about this is my sister is in Kansas so I get to see her so much more than ever before! All kinds of little benefits to this disease....hahaha.....
Trout Scout

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Lymetutu
Trout
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Lymetutu
He actually does a call in show every Monday pm to help educate people about pain mgmt. He wants people to know you don't have to live your life in pain, there are many alternatives out there. Pain is a symptom and you need to find the cause of that.
What a wonderful doctor. I was really impressed by the show and told him so the next day during my appointment. I hope those of you close to Springfield are listening every Monday. TuTu? Any others?
Pam
About 2 months ago I remembered to tune in and I surprised him with a call on the radio! I just thanked him for his care. I think I embarrassed him a bit! He's so humble!
He said, "I promise I didn't put ***** up to this!"
The next time I was in his office, Rose said they heard me call and thought it was great.
You know, it's time for another get together in doc's honor.....anybody game??
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Lymetutu
[This message has been edited by Lymetoo (edited 28 July 2003).]
When I walk in the office a little down, it never lasts because he quickly builds you back up, and you leave there knowing you will get well. He truly is terrific!
I actually look forward to my office visits with him, and I usually walk in loaded with questions. Dr. C answers them all before I leave.
Do make that appointment with him quickly...and you'll be on the road to wellness. He wants you well...that's his goal for you.
Each patient gets his undivided attention. The staff is equally as terrific.
There is no finer LLMD. That's my story and I'm stickin' to it!!!
Cheers,
lifeline
I just read all the replys on Dr. C in Missouri and I am also a patient of his since September of 2000. The first visit I had with him he even prayed for me. That was a first doctor that ever done that and it really impressed. His encouragement is fantastic. He is totally honest with you also. I would like to hear from some lyme patients that are having head, neck and shoulder problems. I have so much pressure in my head it is scarry. My bones are also beginning to hurt. I have swelling in my face, neck and shoulders. This is the first time I have shared this and I hope someone can give me some advice on what helps them.
Thanks
Margaret Castellaw
I told Steve (DadOf2's post in Medical) that this would be a great post for his mom to read.
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Trout
I am now off of all of my meds for 7 weeks as of today!
I have not "fired" him yet because I am not sure what is going to happen just yet, but I FEEL WONDERFUL!
Is there hope? YES!
Does he know what he is doing? YES!
Would I have a life without him? NO!
Do I give him all the credit? YES/NO!
I have been working in combination with Dr. Crist and some natural stuff. I truly believe that it is a combination of the two, which Dr. Crist also encourages, balancing the body, has contributed to my "success so far"!
Would I recommend him? ABSOLUTELY! Without him, I honestly do not think I would be here today!
Dr. Crist, keep up the good work, hard studies and the faith and belief you have in these people and God!
Together, we will all win!
God Bless You!
JJ
hypercoagulation
Hypercoagulation, or thrombophilia, may be defined as a greater
tendency than normal for blood to coagulate, or clot. Of
approximately 500 borreliosis patients that I have tested, 90 percent
have hypercoagulation. Comparatively, only five percent of the
general healthy population has
hypercoagulation.
Two major aspects of hypercoagulation are infections and hereditary
or genetic abnormalities. Chronic infections such as borreliosis,
Epstein-Barr virus, cytomegalovirus, human herpes virus 6 and
mycoplasma have all been associated with hypercoagulation. These
infections appear to be the driving force behind the greater tendency
to form blood clots. Infections may elevate levels of fibrinogen,
fibrin, thrombin/antithrombin complexes, fragment 1+2, and Factor II
(prothrombin)
activity.
When you get a cut, the fibrinogen in your blood converts into
fibrin, which in turn forms a mesh to create a blood clot to help
stop the bleeding. Antithrombin binds to thrombin to form a complex
to prevent thrombin from causing blood to clot. Antithrombin
protects against too much clotting, when it binds
thrombin.
When thrombin is forming a clot it produces fragment 1+2.
Prothrombin (Factor II) converts into thrombin, which causes blood to
clot. When these coagulation components are high, it indicates that
the blood has a greater tendency to clot.
Inherited or genetic disorders may also predispose to blood
clotting. Some of these hereditary defects include antithrombin
activity deficiency, protein C activity deficiency, protein S
activity deficiency, Factor II gene mutation, APC resistance
(Activated Protein C resistance is also called Factor V Leiden
deficiency), elevated lipoprotein(a) or Lp(a), elevated PAI-1
(Plasminogen Activator Inhibiter-1), and elevated homocysteine.
Hereditary hypercoagulation test panels are abnormal in 74 percent of
borreliosis patients, as opposed to about two to five percent of the
general healthy population.
Treatment for hypercoagulation caused by infections is heparin, which
is a blood thinner. Typically, heparin is given subcutaneously
(under the skin) by injection twice a day in low doses for not more
than nine months. It can also be compounded into a troche that
dissolves in the mouth, but that is usually more expensive and is
often less effective than injections.
Symptoms that improve with heparin are pain, fatigue, cognitive
problems and neurological problems. About 80 percent of borreliosis
patients feel better with heparin, and it has been a safe treatment
so far. (One patient did develop bleeding from the rectum, but then
a colonoscopy revealed a colon cancer that had not yet spread to the
local lymph nodes. In other words, the heparin unmasked a hidden
malignancy, so in this case the side effect was a blessing.)
Heparin is not only a blood thinner, it is also anti-inflammatory,
antiviral, antibacterial, and may even be anti-cancer (unproven).
Therapy with heparin usually lowers the level of the coagulation
components fibrinogen, fibrin, thrombin/antithrombin complexes,
fragment 1+2 and Factor II activity. This is desirable, because
elevated levels of these coagulation components can cause decreased
capillary blood flow, if they are high enough. Capillaries are
microscopic blood vessels that are about eight microns wide. A
normal red blood cell, which travels through the capillaries, is
about seven microns wide. When elevation of coagulation components
occur, they could conceivably attach to the inside surface
(endothelial surface) of capillaries, thereby narrowing them. For
example, fibrinogen attached to the inside surface could make it
harder for a seven-micron-wide red blood cell to squeeze through the
narrowed capillary. Reduced blood flow in capillaries would in turn
reduce oxygen and nutrients, and reduce removal of toxins from
tissues. It stands to reason that if heparin could improve blood
flow, antibiotics and hormones would be more effective because they
could pass through capillaries easier.
Life is in the blood. Less blood flow means less "life," and
possibly more symptoms and diseases -- perhaps even death.
Hypercoagulation is associated with other chronic diseases, not just
borreliosis. It is my opinion that how hypercoagulation is treated
will become a paradigm shift in medicine, once further research has
been accomplished.
back to Borreliosis
� 2003 Dr. Charles L. Crist, MD. All Rights Reserved.
healing thoughts,
Wallace
A lady friend of mine would probably come with me. Is there a place closeby to stay that doesn't cost a fortune?
Thanks in advance and God Bless Us All,
Pam
Hope all these beautiful accolades will be copied and placedin a lovely binder to take to him.
He deserves to have these as a tribute to his care and dedication to all of you.
I have not had the priviledge of meeting him, but my sister, Chocolat, sees him and thinks the same as all of you. She's on her way to visit me arriving tomorrow so she doesn't know about this post.
I'll show her when she gets here and she can reply with her thoughts about this wonderful physician who obviousely believes the oath he took, "to do no harm"
So when I went to see my previous LLMD I guess I really didn't expect that any Lyme dx would be forthcoming since dr. shoe was so convinced. My favorite thing about a gifted lyme doctor is that he can finish your sentences for you. By the time you reach the right doc, you need that. You are too tired to speak anymore.
Funny thing about the costs of Lyme. I used to think to travel to see a doc was too expensive. But now I think it is too extensive to not go that route. I'm just feeling blessed that all those other lyme patients paved the way for me.
Lymielu
texastoast
If you go through OK City, OK it's about a 13-14 hr drive. You can also go thru Muskogee.....then to Joplin, then to Springfield.
Well worth the trip! Email me! 
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Lymetutu
If you're a patient of Dr C's and haven't posted here, please add your info!
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Lymetutu
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Lymetutu