LymeNet Flash: LLMD who follows Burrascano's Protocol in CA or out of state too

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD who follows Burrascano's Protocol in CA or out of state too

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Author

Topic: LLMD who follows Burrascano's Protocol in CA or out of state too

muddyfeet
Member
Member # 26633

posted

My current LLMD, or actually her LLNP, says they use Burrascano as a reference.

I really want to find someone who truly knows and goes by Burrascano.

I've been on treatment for 4 months, which I know is not long, but I have felt no improvement and I've read that after 4-6 months if you have no improvement your treatment should be changed.

I also am attempting the low carb, high fiber, high protein, low glycemic diet (as a vegetarian) of my own accord.

In addition, no one has mentioned the exercise Burrascano says is so important.

I just feel like I need more guidance based on Burrascano.

I live in San Diego but would be willing to travel both in and/or out of state for the right LLMD who really uses Burrascano and would do phone consults.

Thanks

--------------------
Labcorp 6/10: IgM + 41, 39, 23

IGenex 7/10:
IFA Ind
IGenex/CDC IgM +:
18+, 23-25+, 30+, 31+++, 34++, 39++, 41++, 58++, 66+, 83-93+
IGenex IgG +:
31+, 34 IND, 41++, 58+

No memory of tick/rash. Sick 1/09. Diagnosed CFIDS 7/09. Diagnosed Lyme 7/10.

Posts: 56 | From San Diego, CA | Registered: Jun 2010 | IP: Logged |

jblral
LymeNet Contributor
Member # 8836

posted

Recommend you join the CaliforniaLyme on-line support group:

http://health.groups.yahoo.com/group/CaliforniaLyme/

There are members in your area who can tell you about doctors.

Also, the California Lyme Disease Association website maintains a list of support groups throughout the state. Check for one in your area:

http://lymedisease.org/california/california_support_groups.html

Posts: 991 | From California | Registered: Feb 2006 | IP: Logged |

muddyfeet
Member
Member # 26633

posted

Hi jblral,

Thanks for the info. I am a member of the CA Lyme yahoo group and posted there as well but have not gotten a response.

One reason why I'm willing to go out of state. If there is an excellent LLMD out of state with a proven track record of getting people better then I would seriously consider going to them.

I will ask at the next San Diego support group. Good idea.

--------------------
Labcorp 6/10: IgM + 41, 39, 23

IGenex 7/10:
IFA Ind
IGenex/CDC IgM +:
18+, 23-25+, 30+, 31+++, 34++, 39++, 41++, 58++, 66+, 83-93+
IGenex IgG +:
31+, 34 IND, 41++, 58+

No memory of tick/rash. Sick 1/09. Diagnosed CFIDS 7/09. Diagnosed Lyme 7/10.

Posts: 56 | From San Diego, CA | Registered: Jun 2010 | IP: Logged |

Remember to Smile
Unregistered

posted

Sorry you've not seen much progress in your tx yet.

Several states are blessed with ILADS-active LLMDs who successfully help LD patients into long-term remission.

If you don't find an excellent LLMD in Ca, select several states to which you'd enjoy travel, then start a new post (or change title of this one) to include just one or two other states.

States with some of the best U.S. LLMDs:
CT
MD
NY
PA
VA

Best wishes,
Smile

IP: Logged |

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