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Lyme Disease ForumsGeneral & SupportNew to lyme in past few months...
01/02/2012 07:58 PM
sebnova81
sebnova81
 
Posts: 624
Member

I started having health issues in August. It all started with a horrible flu-like state and then plateaued to a point where I felt horrible and not myself since then.

I went to the ER, numerous dr's and everything was 'normal.' I finally asked my dr. to do lyme testing and I was positive in both tests.

Just had my first LLMD visit last week (fiance and I made a 3 day trip out of it) and it went well. I have been on doxy since I was diagnosed in late Nov and he upped the doxy and added zith.

He was VERY optimistic that I'd be back to normal by summer and didn't seem too concerned since I caught it early.

I am anxiously awaiting results from the coinfection tests etc... he acted like he didn't think I had a coinfection, he said maybe 30-40% of people with lyme disease have one.

He also advised me to not spend so much time on msg boards (ironic that I'm posting here haha) since most of the people have chronic lyme's and I am in a different boat, which is probably true because I scared myself half to death the past few months reading msg boards and people's stories.

I have felt like I've had a setback the past couple days (maybe because of the upped doxy and new med?).

I start my new job in Feb and I have to study for boards and take them in the next couple months (can barely study bc of poor concentration/dizziness etc...) LLMD wrote me a letter so I can take boards un-timed!

The past 4 months have felt like hell to me and my fiance and I have learned so much about the mysterious controversy and topic of lyme disease.

I just cannot believe that this almost conspiracy exists and so many people's lives have been affected. It is horrific.

Post edited by: sebnova81, at: 01/03/2012 08:53 AM

emphasized, bettyg, leader

Post edited by: Bettyg, at: 01/04/2012 04:24 AM

Treating lyme, bart and babs

Hoping for better days in the near future.

"To be yourself in a world that is constantly trying to make you something else is the greatest accomplishment." -Ralph Waldo Emerson
Reply

01/03/2012 02:55 AM  Top
Bettyg
 
Posts: 26472
VIP Member
I'm an Advocate

Welcome to MD JUNCTION! I'm so glad you found us! You’ve come to the right place for education and support!

Private messages DELETED in 30 days!

ARCHIVE, upper right!

My WELCOME LETTER is posted at the top of SUPPORT FORUM in sticky pin full of good info and HYPERLINKS ready to be read.

http://www.mdjunction.com/forums/lyme-disease-support- forums/general-support/2356916-bettygs-welcome-letter-wgood- beginner-links-

The most important things are at the top; MUST READ and print off as mentioned there already to start your lyme/co-infection journey with us all.

The 1st things to do are:

• JOIN LYME BOARD;

• Post in LLMD REQUEST FORUM for a LYME LITERATE md; see my welcome letter and the INSTRUCTIONS there if you are SPECIALLY FROM CALIF. Where it’s broken down into 8 NAMED AREAS.

• You’ll need to give me my calif. NAMED area where you live in the areas shown there in SUBJECT LINE plus if it’s for ADULT or a child; we need age of CHILD; some llmds have AGE restrictions.

• OTHER STATES will show the SPECIFIC NAME OF THEIR STATE and closest, largest city to them in SUBJECT line plus adult or child; UNDER 21; we need their age!.

http://www.mdjunction.com/forums/lyme-disease-support- forums/llmd-info/Itemid=217/func=post/do=reply

• Also, I’ll need the following info in your request post:

in your llmd request, please EDIT and add more info ok.

Are you UNDER AGE 21;; if yes, I need your age shown as some of our llmds have AGE RESTRICTIONS; thanks!

how long you've been sick

if you've tested for lyme/co-infections;

which labs doing work for which specific test, etc.

did you have western blot igm/igg done by igenex?

if yes, what were the POSITIVE & INDETERMINDED numbers; NOT negatives.

thanks for understanding; just EDIT your post. you can find all by going to left MY DISCUSSIONS, click on it.

after you add more, i'll send you names ok.

just send me a PRIVATE MESSAGE left side, giving me the direct link to come to here, and i'll send you the names ok big thanks.

Betty’s suggested posting guidelines:

Many of members have neuro lyme, and it is hard to read long solid block text and be able to comprehend; example, me, 42 yrs. neuro chronic lyme, so we are UNABLE to comprehend and read. Thank you for helping us help YOU Wink

please post in short paragraphs like you see below or look at a few other posts, but we neuro folks need them short.

1-2 sentences MAX per paragraph and hit ENTER TWICE to doublespace between each paragraph. We’ve lost our comprehension skills to read solid block text.

we neuros lose our train of thought if the sentence is broken up in the middle; so please keep an ENTIRE sentence together as ONE. hugs

For easier reading, please edit your post. You can break up your longer paragraphs into smaller paragraphs. Please hit ENTER key twice after each paragraph.

Go to left hand corner; click edit send. Then go to bottom and click SUBSCRIBE TO THIS DISCUSSION.

Thank you for posting in a manner that makes it easier for all to read and help others.

bettyg, llmd coordinator/group leader/iowa activist

****************

hi Wink please EDIT your post and break it up using my guidelines above so we neuro lyme folks will be able to read/comprehend it.

thanks for helping us help YOU Wink

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

01/03/2012 06:42 AM  Top
waxby
waxbyPosts: 4108
VIP Member

~~~Hello sebnova, Welcome!

~~~Re your " He also advised me to not spend so much time on msg boards (ironic that I'm posting here haha) since most of the people have chronic lyme's and I am in a different boat, which is probably true because I scared myself half to death the past few months reading msg boards and people's stories."

~~~It is good (you know what I mean) to see you here with us chronic sickoes. It is good that you are scared. Sorry. What I'm saying by this is that if you are very fortunate, you will not become one of us.

~~~So this is to say stick with your treatments until at least two months past NO symptoms before even thinking of stopping yet, even IF this takes years, yes years!

~~~Here's some info to help you get started ...

~~~Hello Newbies ...

~~~Lyme cannot be treated as a lone entity.

~~~Lyme Disease can be, and often is, a very serious, chronic persistent, potentially dangerous and life threatening, COMPLEX disease, and so, Lyme Complex Disease, or LCD, most often with any number of co-infections, such as Babesia, Bartonella, Erlichia, and many more, that must be treated before Bb, Borrelia burgdorferi, or Lyme, one by one, or simultaneously until at least two months of symptom freedom before even considering stopping treatment yet!.

~~~LCD knocks your whole body/mind/spirit out of sight. You need to rebalance, and rehabilitate your whole being!

~~~It IS important to realize that each of our needs, and symptoms, are unique and require our careful and discerning, educated, well read, attention.

~~~And there is no magic cure or magic DR or magic clinic. And there are a lot of "snake oils" and "snake oil salesmen" out there, so be cautious!

~~~Some find relief or remission from conventional/pharmaceuticals alone or naturals/alternatives such as herbs etc alone or a combination of any.

~~~AND, relief or remission from ONLY long term treatment, even years, in MOST IF NOT ALL chronic persistent cases. That is, if not caught immediately and treated with at least three months of antibiotics, and not necessarily for longer ONLY if symptoms are not present after the first month and through the second two months of treatment!

~~~We each have our own combination lock, code, puzzle, conundrum, or mystery to figure out.

~~~Here is another of the main issues with Lyme Dis-ease...

~~~If you do not see a Lyme Literate Dr. (LLDr), and your tests APPEAR “negative,” (or positive), they may treat you for whatever symptoms that your symptomology SEEMS to fit.

~~~Also, by not seeing a LLDr, a non-LLDr will normally follow the IDSA’s guidelines, rather than the ILADS’ guidelines, http://www.ilads.org/files/ILADS_Guidelines.pdf , or a LL, Lyme Literate/ILADS/IGeneX Lyme Disease test, and so may declare you negative of Lyme Disease based on false standards of detection, including not basing your diagnosis of LCD on symptomology and pathology, even with a “negative” Lyme test.

~~~And in most cases, if you are or are not being treated for the actual culprit, LCD, the phantom treatments for mocking symptoms will do almost nothing or nothing at all or even cause more problems.

~~~Incorrect treatments can even do damage, such as being treated for MS, which Lyme mocks, with steroids, or any other drug designed to suppress the immune system, etc, that will only intensify the Lyme invasion and wreak additional havoc inside of you and on your life.

~~~Some have even been prescribed surgery, by a non-LLDr for a Lyme mocking "phantom" problem and the surgery, in many or most cases, failed.

~~~Lyme dis-ease can mock 300 dis-eases and exhibit hundreds of symptoms, in any number or combinations and timelines, coming and going, and to be repeated or not.

~~~However it remains important to carefully rule out other possible problems.

~~~But, let an LLDr do this to save you many middle steps.

~~~If you are working with, WORKING WITH (as in not blindly following) a Dr, hopefully a LLDr, Lyme Literate Dr, OR only with yourself as your healer, if you so choose for your own reasons, pay careful attention to your reactions to each potential remedy.

~~~If the reactions are much too intense, and you are monitoring and comparing them to possible allergic response and …

~~~having carefully ruled out adverse allergic response, as many reactions are the "herx", the Jarisch/Herxheimer reaction to therapies that actually make you feel worse before better, and are a sign of effective therapy, and may be indicative of probable Lyme Complex Disease …

~~~try trimming down, ramping down, dosages to 1/2 or 1/4, even as much as 1/8 the dosage in some cases, to find your personal, more tolerable, not overly aggressive, therapeutic dosage, and then "ramp-up" slowly and carefully.

~~~And always take probiotics between doses of antibiotics, two hours before and after dosing are a good rule-of-thumb. ANTI-biotics kill unfriendly as well as friendly bacteria and so the intestinal flora must be re-constituted with the friendly PRO-biotics.

`````````````````````````````````````````

~~~There is a general consensus to get a superior diet in order.

~~~That is, no junk. Everyone with any sense whatsoever knows what that is.

~~~This means no sugary sodas or even diet ones or any carbonated dead beverages. Pure junk!

~~~No processed sugar either. No empty calories!

~~~Only nutritiously dense foods in a wide variety of the rainbow such as fresh mixed sprouts, purple and green cabbage and mixed greens salads, mixed berries, etc.

~~~Mostly if not all vegetarian.

http://www.secrets-of-longevity-in-humans.com/vegetarian- protein-sources.html

http://www.vegparadise.com/protein.html

http://www.vrg.org/nutrition/protein.htm

http://makingpages.org/health/myths.html

http://sugarrocket.com/vegan/vegan-myths.php

~~~Mostly if not all raw - fresh unheated fruits and vegetables are raw.

~~~Little to no dairy.

~~~Cut out gluten, wheat, rye, oats, and bran, if you happen to be gluten intolerant, as many Lyme Patients are.

~~~Eat whole grains and brown and wild rice blends, quinoa, amaranth, buckwheat, etc.

~~~Raw nuts and seeds, raw, so as not to destroy living enzymes and essential fatty acids, such as raw walnuts, almonds, pumpkin and sunflower seeds.

~~~Beans, such as kidney, black, and garbanzos.

~~~Cooled down teas to warm (under 110 degrees) with some almond milk and a couple of ice cubes etc (not hot, so as not to destroy living enzymes in raw honey and raw choc if added.) You should be able to hold your finger in it and just feel the warmth, not hot...

~~~Green tea, red (rooibos) tea etc, almond milk, etc, raw honey, raw cocoa powder. Yum!

~~~You could vigorously stir into the warm mix a Tablespoonful or two of some organic chia seed (from health food store, and drink it through a straw, unless you want a chia pet mustache!) and/or freshly ground flax seed.

~~~You could also vigorously stir in some brown rice protein powder (from "NutriBiotic") and brewer’s yeast (from "Lewis Labs" - no this is not the yeast that contributes to yeast growth problems, and is very nutritious and a tasty brand), and also some raw maca powder.

~~~I make a mixture in equal amounts of brown rice protein powder, raw maca powder, and brewer’s yeast and use a couple of tablespoons of this mixture in my breakfast tea.

~~~I also include in my breakfast tea my own brewed chai mixture, in descending order of decreasing amounts, of cinnamon, ginger, cardamom, nutmeg, turmeric, cloves, and black pepper. Google each of these spices to learn of their benefits. Mix a big batch of these beneficial dry spices and keep it in an airtight jar in the fridge.

~~~Stir one or two teaspoons of this mixture into a cup of cool water and bring to a boil and stir and pour into tea mug and let steep and settle for about five minutes. Pour slowly and gently into another mug leaving the settled “mud” at the bottom of the cup behind to discard.

~~~Plenty of water, between meals, some with freshly squeezed lemon, for detoxifying, one simple, of many methods critical for consistently, persistently, clearing toxic load from our bodies.

~~~A good rule of thumb for quantity of water to drink is to divide your body weight number in pounds in half, and use that number for number of ounces of water to drink each day.

~~~Go to a health food store and get a sprouting kit and make your own mixed sprouts at home in your kitchen.

~~~Try 2 Tablespoons of broccoli, 2T fenugreek, 10T(5oz) mung bean sprouting seeds in a half gallon sprouting jar.

~~~In three to five days, depending on the temperature, Winter or Summer, and poof, nutritiously dense food.

~~~Don't rinse on last day to keep on dry side to keep longer in fridge. They'll keep for a week in the fridge in an airtight container. Leave uncovered overnight in fridge the first night to chill and breath out initial condensate and then cover and leave covered.

~~~Start a new batch some days before they run out to keep a constant supply for sandwiches, salads, etc. Add it to a big mixed greens salad.

~~~Omega 3 fatty acids and fiber rich seeds such as chia (whole or ground) and freshly ground flax-freshly ground flax as the omegas become unstable after some time after being ground, and flax is indigestible whole. Unheated so as not to destroy vital omega fatty acids and living enzymes.

~~~I use 2 tablespoonsful of whole organic flax seed and grind it fresh in a coffee grinder each time I use it. I stir this vigorously into 16 ounces or more of tepid water and soak for five minutes to absorb water and expand and then drink this through a straw 30 minutes before meals.

~~~I continue to drink more water in between meals away from food for better digestion and elimination.

~~~Drinking liquids with meals only dilutes your food not allowing it to digest more properly.

~~~Drinking this flax/water mixture gives digestive/elimination system a jump start ahead of meals in order to capture more bile and transport it out of the body, so the bile is not recycled back into your body, as is what happens to the bile, thus ushering the bile's excess cholesterol and toxic load out of the body. Your body will readily produce more fresh unpolluted bile.

~~~Flax (as well as chia) also contains essential omega 3s and 6s in a healthy proportion of 3 times more 3s than 6s. Most diets contain way too many 6s than 3s.

~~~Corn oil has 46 x more 6s than 3s, very bad. Olive oil has a ratio of 3-6s to 13-3s, very good. We tend to get way more 6s than 3s, not good.

~~~Your body will convert these essential fatty acids into necessary DHA and EPA.

~~~Organic everything as much as possible.

~~~No harmful habits such as smoking etc, or alcohol, which is very bad for many Lyme patients.

~~~As examples, out of hundreds of potential remedies, I have done MMS, and in alternating days, frequencies, amounts, and combinations,

~~~teasel, samento, venus fly trap, banderol,

~~~smilax, Japanese knotweed/resveratrol, andrographis, ("Buhner's Herbs from his book "Healing Lyme.")

~~~Dandelion and parsley extracts, mangosteen extract, olive leaf extract, grapefruit seed extract, bromelain, systemic enzymes, nattokinase, or better, lumbrokinase, Graviola, Sangre de Drago, Jatoba (these three are South American rainforest herbs)

~~~vits, mins, supps, baking soda, superior diet.

~~~And for about a year 100mg a day or every 2nd, 3rd, or 4th day, week, or month of minocycline.

~~~However, for now, I am only doing the MMS and at one to three drops one to three times a day, even skipping a day or more as I am very ill and for many years, as I think I am doing too much too soon for my level of infection.

~~~And now doing HBOT, Hyperbaric Oxygen Treatment, IM Rocephin, Myers' Cocktail IV, Medical/pharmaceutical grade supps, vits. coloidal silver.

~~~However, (update) now …

~~~I am doing every day MMS, Minocycline, Azithromycin, and Rifampin. Rocephin IM, (breaking), Atomidine (hoping to replace Armour Thyroid), HBOT (hyperbaric oxygen treatments, 85 dives and taking a break), Myers Cocktail IV plus glutathione (vits, mins, + glutathione) twice a week, (taking a break), Byron White's A-Bart and A-L pulsing and ramping up very slowly starting with 1/16 of a drop each twice weekly, Samento, Banderol, Teasel Root, vitamins, minerals and supplements ... pondering the seen and un-seen …

~~~Your symptoms will change, come and go, see-saw, roller coaster, scare you, tickle you, nauseate you, turn you shapes, colors, and sizes, make you laugh, make you cry.

~~~Hold tight! This is some Amusement Park!

~~~This forum is your refuge. We "get" you. USE IT!

~~~And remember, "this is a marathon and not a sprint." Be the turtle, not the hare. Moving too quickly could be potentially harmful.

~~~Chronic, persistent Lyme Dis-ease can take a very long time to diminish towards remission. It must be approached carefully, systematically, persistently, patiently...

~~~And ... Never give up!

`````````````````````````````````

~~~On ramping and pulsing...

~~~When a remedy dose hits too unbearably hard, your dose may be too high, and that is after making certain this is not an allergic reaction.

~~~Take a day or two or three off , if you must, until the "Herx" calms down to a reasonably, more tolerable manageable, level, and begin again, every other day, or more, if you must, thus pulsing...

~~~Begin again at a lower more tolerable dose, if necessary, such as 1/2, 1/4, or 1/8 the dose thus ramping down.

~~~If one more dose hits too hard again, take every other or third day off, pulsing, until you arrive at a more tolerable Herx event level and tolerable therapeutic dosing level.

~~~As your Herx effect lessens over time, begin turning up the volume by adding back some dosage level, ramping up, and then closing the pulsing gaps.

~~~And always take PRO-biotics between doses of ANTI-biotics to re-constitute intestinal flora as ANTI-biotics destroy both bad and good bacteria. Take pro-biotics, breaking open the capsule, if acid resistant strain and not in an enteric coating, starting in your mouth, the beginning of your digestive system, 2 hours before and after dosing, after anti-biotics have cleared the stomach and intestines, are a good rule-of-thumb.

~~~Unfortunately, feeling worse before feeling better, the Herx, is par for the course, but is a useful gauge for pulsing and ramping and consistently, persistently, keeping fire under the critters butts.

```~~~from my straight jacket~~~out on a limb~~~lookin like a cocoon~~~hangin by a thread~~~waitin for a butterfly~~~under the moon~~~Lovey-Dovey, Mitchell~~~

Post edited by: waxby, at: 01/03/2012 06:43 AM

Post edited by: Bettyg, at: 01/04/2012 04:20 AM

~~ "The way to 'Heaven' is to bring it with you ..." -Mitchell
~~ "Sometimes, we gotta go through hell to get to 'Heaven'" -Mitchell
~~ "The way out is in" -Mitchell
~~ "A miracle speaks ...'I don't believe in Miracles.' " -Mitchell
~~ "Life is good, even when it isn't." -Mitchell
~~ "Sometimes you gotta lose to win." -Mitchell
~~ "It's easy when it's easy! Find reason, purpose and meaning when it's hard!" -Mitchell
~~ "If you're gonna think, think again!" -Mitchell
~~ "Make it so!" ...
~~ “When life do what it do, as it do-do, simply say ‘Of Course!’ (to soften life’s ‘blows’)” - Mitchell
~~ A master once said, "When embarking on the spiritual path, 'Oh Dear! There's no turning back! You've really done it now!' "
~~ “Not thoughts be your guide, rather, guide your thoughts.” -Mitchell
~~ "That which is within, and that energy entering this body/mind/spirit, causing harm and ill health, must and will be transformed into love healing energy and sent out in every direction" -Mitchell
~~ One morning ten years ago I awoke from a dream chanting over again and again, and writing this down so as not to forget ... "It doesn't matter who did what, there's nowhere else to go but up ..." -Mitchell
~~ "This life, our life, and what we do with it on this planet is “simply” a display, a reflection, of what is going on in our consciousness. The proof is in the puddin’. Look at our planet, what humans are doing to it, and with it, and to one another, and ask yourself ... ~ 'How’s this working for us/me?' ” -Mitchell
~~ "Step away from monkey mind, not tangle ... Observe ... Inhabit your higher self ..." -Mitchell
~~ "Anything is possible, but manythings you think are true, are not ... " -Mitchell
~~ "Grow where you are planted ..." -Mitchell
~~ "Change your future now ..." -Mitchell
~~ “Write your equation … 4 u r the sum of u … “ -Mitchell
~~ “We are largely a product of our environments … how’s your inner environment doing? …” -Mitchell

Previous discussions I participated in:
going out of my head
NEEDS ADVICE & SUPPORT
Am I crazy?

01/04/2012 04:30 AM  Top
Bettyg
 
Posts: 26472
VIP Member
I'm an Advocate

hi seb Wink

thanks so much for breaking up your above post so neuros like me could read/comprehend it all.

yes, you've learned the hard way like us all that WE ARE THE VICTIMS TWICE; as patients in a lyme/co-infection war we wanted NO PART OF!

what will be your specialty after passing your boards?

co-infections, please go to my welcome letter at top of support and look for the LYME FACTS area from dr. corson's KID'S EVALUATIONS apply to adults except meds/dosages are different. she explains the entire body and WHICH DISEASES affect those parts; you'll have a good idea what you DO HAVE by the time you finish reading it.

STAY ON MESSAGES BOARDS; you won't be lied to; we tell it like it is since we've all learned the hard ways.

we'll direct you to LYME FACTS/REPUTABLE ONES, etc.

we'll give you support, need a shoulder to cry on, to vent, and to learn by, we're here for you/fiance 23/7 daily.

we walk in your shoes; we feel what you are feeling. we have many in college here trying to graduate, and much to young to be going thru all this hell.

did you get the llmd name from us or SOMEONE REPUTABLE?

hugs/prayers to you/fiance,

bettyg, llmd coordiantor/leader

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

01/04/2012 08:44 AM  Top
sebnova81
sebnova81
 
Posts: 624
Member

Thank you, Bettyg. I just graduated with my doctorate in occupational therapy. I will be an occupational therapist in a skilled nursing facility...working with people who have been in the hospital and have used their insurance days, but aren't ready/independent to go home or to their prior living situation.

I am confused about the prevalence of coinfections. My LLMD didn't seem to think I had any of them and from I've read, I don't feel like I do? I should hear back about all the blood test results this week...I am nervous. It seems like some people thing everyone who has lyme has a coinfection and then some (including my LLMD) say that it is a minority (30-40% or so). We'll see...

Yes, I found my LLMD through a reputable source and he follows ILADS and all that jazz.

Thanks for your reply!

Treating lyme, bart and babs

Hoping for better days in the near future.

"To be yourself in a world that is constantly trying to make you something else is the greatest accomplishment." -Ralph Waldo Emerson

Previous discussions I participated in:
Revised original Introduction and Story

01/04/2012 03:00 PM  Top
Bettyg
 
Posts: 26472
VIP Member
I'm an Advocate

seb, Yes, I found my LLMD through a reputable source and he follows ILADS and all that jazz.

OUTSTANDING ... and all that jazz; i loved that song!! reading that phrase took me to it immediately.

great, you read dr. corson's kid's evaluatin and you feel you don't have co-infections; fantastic. blood tests will confirm majority of the time.

best wishes; thanks for sharing your occupation; i thought you were going to be a LAWYER PASSING THE BOARDS!!

you've got a great job also; i/hubby have used your co-worker's skills to give us back quality of life; thanks for chosig this occupation.hugs/prayers,

bettyg, leader

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

01/04/2012 03:48 PM  Top
sebnova81
sebnova81
 
Posts: 624
Member

Thank you, Bettyg!

It took me a long time to discover OT, but I think it will be worth it. I know I want to help people somehow, so hopefully I'll be able to!

Now if only I could get feeling better myself, so I can help others.

Thinking I should hear back on blood test results by the end of the week, fingers crossed for good news.

The addition of 500mg of zith and upping doxy to 300mg this past week has made me take a step back I feel like. It is prob herx?

Is it okay to take low doses of xanax?

Treating lyme, bart and babs

Hoping for better days in the near future.

"To be yourself in a world that is constantly trying to make you something else is the greatest accomplishment." -Ralph Waldo Emerson

Previous discussions I participated in:
Revised original Introduction and Story

01/04/2012 03:54 PM  Top
Bettyg
 
Posts: 26472
VIP Member
I'm an Advocate

you asked if it's ok to take lower doses of xanax when herxing?

none of us have MEDICAL backgrounds; sorry. so we can't tell you about. since you're in calif??, are the drs. offices still OPEN to call and ask them.

xanax s mood/depressant; they are the ones to ask. sorry...bettyg

logging off to nap before supper.

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

01/04/2012 04:01 PM  Top
sebnova81
sebnova81
 
Posts: 624
Member

I actually am in NE. LLMD said it was fine to take xanax, I just am nervous for becoming dependent or something.
Treating lyme, bart and babs

Hoping for better days in the near future.

"To be yourself in a world that is constantly trying to make you something else is the greatest accomplishment." -Ralph Waldo Emerson

Previous discussions I participated in:
Revised original Introduction and Story

01/04/2012 09:22 PM  Top
Bettyg
 
Posts: 26472
VIP Member
I'm an Advocate

seb,

boy, do i understand about your not wanting to get addicted to anything.

my late MIL had diabetes 2; lost her toes first, then her leg to her knee. she was given PERCODAN pain pill for her phantom pain, etc. she became addicted to it; was a smoker too.

i'm on xanax. when we need the extrahelp to keep our mood swings and/or depression under control; don't feel guilty or it's a crutch.

it's a NECESSITY during this time in our lives. when we make progress, it may become a thing of the past. we won't know until we reach that level; but it's our friend to help us thru bad times now. that's my outlook on it anyway.

glad you called your llmd for guidance. we all want to help you, but that's where our llmds and their professional medical degrees come into place.

we can give you all the moral support you need when down, when venting, or needing some accurate sites to get good info from.

i didn't know we were neighbors nebr!! unfortunately, you have no llmds in yoru state. if you com across any i don't know about, please share that info by private message, pm is under my name.

this is the info i try to get on all our llmds/llnds, etc:

full name

specialty

street address

city/state

phone

fax no.

website

email IF possible

1st visit charge $

length of time

followup visit $

length of time

do they treat KIDS; WHAT AGES?

what insurances do they take

do oral & IV?

what lyme labs used?

thanks seb Wink best wishes my new OT friend, hugs/prayers,

iowa activist, bettyg, leader

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
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