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Lyme Disease ForumsGeneral & Supportlyme and severe anxiety
04/12/2012 11:40 AM
leahhenry
 
Posts: 3
New Member

I just recently did a slow taper off of a benzodiazapine and despite getting completely off it, the anxiety was so intense I felt like it was eating me up so my doctor advised me to back on it. My doctors felt that I did things backwards in that I should have treated the Lyme agressively first before coming off meds since lyme has caused me severe anxiety, depression and pain. Has anyone else has an experience like this? Does anyone relate to the terrible anxiety and agoraphobia that comes from this disease? I'm feeling pretty alone right now.Has anyone had an easier time coming off meds once their lyme was treated?

Thanks for your feedback.

Leah

Reply

04/12/2012 11:46 AM  Top
nank59
nank59  
Posts: 815
Member

My most severe anxiety is during major herxes. My anxiety set in when first becoming chronic. I experience anxiety during flares and times of exhaustion.

Sometimes I awaken in a state of anxiety, sometimes it just appears out of nowhere, often when stressed...and in crowded public places, especially when there is a lot of movement and noise.

You are not alone!

I asked a question of General & Support forum just the other day. My husband was not really understanding how anxiety can just occur for no reason. Apparently, it is due to the neurotoxins interfering with the brain.

Sometimes I can just slow my inner body down and breathe slow and deeply. Other times, I just have to go somewhere quiet and often dimmed or dark.

Take care and wishing the best to you!

nan

I am not a doctor, nor have I ever been. All comments are based on my personal experience or opinion.

IgM
41+

IgG
41+
31 IND
39 IND

Currently treating Lyme & Babesiosis.
Have many Bart symptoms.

Blessings! :)

04/12/2012 11:57 AM  Top
leahhenry
 
Posts: 3
New Member

Thanks for your feedback. I appreciate it!

Love Leah


Previous discussions I participated in:
Just finished a benzo taper program

04/12/2012 04:02 PM  Top
Bettyg
 
Posts: 27280
VIP Member
I'm an Advocate

hi leah Wink

please break up your solid block post using my guidelines below so we all can read it.

thanks for helping us to help YOU Wink

bettyg, leader

-----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:

NO ALL CAPS POSTS; they are illegible to me/other neuro folks!

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

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

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.

04/12/2012 05:34 PM  Top
amycwusa1976
 
Posts: 45
Member

Hi Leah,

I've been through almost exactly what you have.

A year ago, I was so sick from Lyme that I was on several medications (I was misdiagnosed) and was having so many side effects, I could ever tell; was I sick from an illness or side effects from meds?

Anxiety, crushing panic attacks really, was absolutely my worst symptom of Lyme. It would take over my body and last for hours.

There were a few meds I came off of before being diagnosed. It wasn't easy, but I made it.

I've been treated for Lyme for 3 months. I have discontinued several meds in the process, it's been the greatest challenge of my life, but I'm much better now.

If I could go back, I definitely would have treated the lyme first. But, I personally believe that before diagnosis, it's easy for docs to treat symptoms with unnecessary meds. The sooner you can rid your body of those meds, you may feel better.

I am NOT saying your med is not needed- I am just speaking about my experience. Docs had me on anti-depressants, sleep meds, anti-anxiety, etc. The whole time the lyme raged inside me.

I hope you feel much better. Lyme-driven anxiety is ust terrible, but you WILL get better. Remember it is just the disease.

A


04/12/2012 06:11 PM  Top
sebnova81
sebnova81  
Posts: 626
Member

Anxiety is one of my worst symptoms, it's horrible! I have to take xanax, otherwise I wouldn't be able to get through work I don't think... I hate it. I really hope it goes away with treatment.

When I wake up in the morning, my brain instantly turns on and I cannot go back to sleep. I used to be the person who would go back to sleep no matter what! It is so annoying.

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

04/12/2012 06:22 PM  Top
kimomile
 
Posts: 346
Member

Same here. I am on an anti depressant until it gets under control. After 3 months of yeast and Babesia treatment I no longer need Xanax. It will be a few months til the zoloft is done. I do NOT want to feel that anxiety again. It was the most debilitating fear I have ever felt. I think my mind has blocked it out.

I'm doing much better now, but still struggling with ovrall craptastic energy and emotions. But I am functioning in the world and that is something to be grateful for. It's like my general "quality of life" expectations are so much lower now. I do hope I will feel joyful again. I miss warm fuzzies.

So yes, I would say, treat the Lyme, specifically Babesia, and your anxiety will get better. In the meantime, use the xanax, or whatever it is. There will come a time when you won't need it anymore.


04/13/2012 08:09 AM  Top
mowgli
mowgli  
Posts: 387
Member

Ditto, awful, awful anxiety. I am buzzing everyday as though I am under threat, the "fight or flight" sensation.

I take Ativan when I can't breath or if I am getting super upset, flustered, angry.

I am hoping the Lyme treatment will also end most if not all of it someday!


04/13/2012 08:27 PM  Top
lymeinmich
 
Posts: 1075
Member

Me too.

Horrible anxiety, and never ever had anxiety b4 Lyme.

Xanax did not work for me. I had horrible crashes when it wore off. It made me feel worse than b4 taking it, so I felt I needed another, and so on and so on...

Recently my LLMD gave me Valium. That seems to work a bit better for me, no highs and lows.

Most days I just try to deal w/o the meds.

I have to believe that this too shall pass.


04/13/2012 08:42 PM  Top
bbl2011
 
Posts: 167
Member

Hi,

While I have no experience with meds and am about to start treatment in the next month or so, one of my few symptoms was crippling anxiety/ social anxiety etc.

I would get anxiety/ panic attacks that didn't just last 30 min to an hour, they would last almost SEVEN DAYS at a time.

The only time my head didn't feel like my head/ eyes weren't going to explode etc was when I was sleeping.

Mild every day stresses exacerbated it majorly.

Then all the sudden recently, with no intervention, it all went away recently, just as mysteriously as it started. Just mild social anxiety comes back here and there.

with that said though,I think if any major traumatic event happened, it would flood back.

Something in my body was able to get a hold on those symptoms. But Lyme does that. It brings on and turns off certain symptoms all the time.

Lyme is a real trip isn't it?

I am not a doctor, nor do I play one on TV. All comments are based on my personal experience or opinion.

* Had a band 23 on Western Blot thru LabCorp 2012
* Bands 39 and 41 thru Clongen Labs 2012
* My Lyme ID test ALL positive thru Neuroscience.
* Have been infected for possibly 10 years
* CD57 60
* My symptoms have all been cognitive (neurolyme), but I have always seemingly stayed functional (even if it didn't feel like that on the inside!).

http://ilads.org/lyme_disease/Psychiatric_Brochure_08_08.pdf

* Have not started treatment yet (as of 4/2012)
* Blessed that the only pain is in my right knee joint, occasionally left.

*I always wonder, how many ppl are walking around, with my type of Lyme infection, just being put on paxil...
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