LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » 24/7 palpitations and shortness of breath

 - UBBFriend: Email this page to someone!    
Author Topic: 24/7 palpitations and shortness of breath
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just wondering if anyone else has these horrible symptoms and why they are there.

Had a complete pulmonary workup. Total cardio workup up to a CT scan of the heart. Negative all around. Having daily palpitations and shortness of breath. still as scary as when they started. So tired of this just kill me already and get on with it.

28, non smoker, and 8 brutal months of this daily. **** lyme.

Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
losferwrds
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Are they palpatations or Tacychardia.
Is it worse when you are standing?

Do this, check your pulse sitting down, then stand up and check it again while standing.
If it jumps like 30-40 bpm it could be
Postural Orthostatic Tachycardia Syndrome
http://www.dinet.org/


If its just palps and breathlessness, it could be from babs and/or bart, and a magnesium deficiency.

IP: Logged | Report this post to a Moderator
feelfit
Frequent Contributor (1K+ posts)
Member # 12770

Icon 1 posted      Profile for feelfit     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hang in there Toppers. It is not an easy illness that is for sure. And then tests that you would think would be abnormal are normal, making you even more confused.

I get the palps and tachycardia too. Not real shortness of breath, but feels like I can't breathe. I think it might be babesia symptoms.

Have you addressed co-infections?

Feelfit

Posts: 3975 | From usa | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
The BPM does not change when I do that. However my vitals are going lower and lower by the month. Pulse and BP just taken were 105/65, 62 h/rate. systolic and diastolic are dropping by like 5 pts a month, it's insane. I started out at 125 / 85 last year.
Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
MorningSong
LymeNet Contributor
Member # 19989

Icon 1 posted      Profile for MorningSong     Send New Private Message       Edit/Delete Post   Reply With Quote 
Toppers~

I too had all the symptoms you described. All my tests came out normal as well. My doctor put me on IV Rocephin for the Lyme and this has helped tremendously.

What antibiotics are you on? Are you seeing a Lyme Literate Doctor?

Posts: 515 | From In His Loving Care | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
None and no. I haven't done the IgeneX test yet. Can I have my doctor put me on trial antibiotics to get a "cheaper" diagnosis instead of dishing out 1k for a complete lyme test?
Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
MorningSong
LymeNet Contributor
Member # 19989

Icon 1 posted      Profile for MorningSong     Send New Private Message       Edit/Delete Post   Reply With Quote 
My Primary Care Physican is the one that diagnosed the Lyme. He ran a Western Blot Test and sent it to LapCorp which came back positive. This test is not 100% acurate, but at least it is a start with your primary doctor until you can get to an LLMD.

Do a Western Blot NOT and Elisa. Doxycycline is what most Primary Care Physicans seem to start with.

Posts: 515 | From In His Loving Care | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
glm1111
Frequent Contributor (5K+ posts)
Member # 16556

Icon 1 posted      Profile for glm1111     Send New Private Message       Edit/Delete Post   Reply With Quote 
Toppers,

I had all of these symptoms. They went away when I treated for Parasites and Worms which play a MAJOR part of lyme disease. Check out


www.lymephotos.com



and also check out the symptom list at


www.humaworm.com

Gael

--------------------
PARASITES/WORMS ARE NOW
RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS*

Posts: 6418 | From philadelphia pa | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
iloveyou
Member
Member # 20244

Icon 1 posted      Profile for iloveyou   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am also having the symptoms.
It is a common sympotm of adrenal fatigue, which basically means your body is low in cortisol hormone from being so stressed from being sick so long, and ALSO it is a sign of Hypothyroidism, and both seem to be common in Lyme disease as I learned from reading
http://www.ilads.org/lyme_disease/B_guidelines_12_17_08.pdf

So, please get that checked by someone who knows what they are doing..PS- ost endocrinologists have NO clue. I am dealing with this now.
Please see www.drlowe.com
BRILLIANT man.

--------------------
Are you also having spiritual problems? Click Here to see if your problems are not just Lyme.

Posts: 42 | From sweden | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
iloveyou
Member
Member # 20244

Icon 1 posted      Profile for iloveyou   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Oh sorry..I forgot to add that it is also VERY common in those who are sick a long time to be short in B12.
Get a sublinguial methycomalbamin vitamin and do not take more than 3000mg a day.
You should feel better right away.

--------------------
Are you also having spiritual problems? Click Here to see if your problems are not just Lyme.

Posts: 42 | From sweden | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
So you say don't take more than 3000 mg a day.

The person who linked the worm thing a couple posts up has a protocol for like 15000 mg a day,.

which is it, rofl. So tired of this, thanks for responses though.

Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
Geneal
Frequent Contributor (5K+ posts)
Member # 10375

Icon 1 posted      Profile for Geneal     Send New Private Message       Edit/Delete Post   Reply With Quote 
Igenex Western Blot only costs $200.00 for IgM and IgG.

Tests numbered 188 and 189.

Magnesium helped me a lot with my heart symptoms.

Palpatations included.

I had a nuclear stress test done and my heart was "perfect".

If your pressure keeps dropping, you may have Neurally Mediated Hypotension.

When you stand up, even sit up from a prone position,

Your blood pressure drops.

When I started mine was 120/80.

About 1.5 years into treatment while visiting my LLMD,

My blood pressure was in the 60's/40's.

I take cortef to help with this.

Water helps as does extra salt in my diet.

Try the B-12. Don't exceed 3000mg a day to start.

Until you know exactly what is wrong with you.

Magnesium you can take until your stool gets loose.

Then you know it is too much and back off a little.

I weigh 105lbs and can take 1000mg of magnesium easily.

Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
glm1111
Frequent Contributor (5K+ posts)
Member # 16556

Icon 1 posted      Profile for glm1111     Send New Private Message       Edit/Delete Post   Reply With Quote 
Topper,

I posted the parasite/worm link. I don't take any b12. I think you are confusing it with the salt/c protocol which i take 20,000mg each per day. Just wanted to clarify,

Gael

--------------------
PARASITES/WORMS ARE NOW
RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS*

Posts: 6418 | From philadelphia pa | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can anyone else verify that parasite website? That's insane

Question: What was the weirdest thing that has happened to you since starting the treatment?
Answer: I had two really strange experiences. The first was when the microscopic worms started to exit my body through my eardrums. It happened after a shower, on two occasions; one hears a crackling noise. Upon further investigation, it was found that the worms were present on a Q-tip. My second strange event was lying awake one night and feeling a microscopic worm exit through the top of my head. Never break the microscopic worm off, let it come all the way out of your body. Just like earthworms, the worms can regenerate, and the remaining half can regenerate in your body. You want to allow the worms to crawl out and desiccate. The next morning, I had a scab on the top of my head. You will feel the worms crawling out of you, especially on your face since your head is where so many of them like to reside.

Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
glm1111
Frequent Contributor (5K+ posts)
Member # 16556

Icon 1 posted      Profile for glm1111     Send New Private Message       Edit/Delete Post   Reply With Quote 
Toppers,

I have had EXACTLY what is pictured in that website pour out of me. The website is legite. Check out lymestrategies. These are the people on the protocol that have Lyme.

Go back in the archives to 2004 when people first started on it. Willy Burgdorfer found Filarial Worms in the ticks and as an aside found the spirochetes.

For me it all makes sense as to why there is so much pain and suffering involved with this disease,

Gael

--------------------
PARASITES/WORMS ARE NOW
RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS*

Posts: 6418 | From philadelphia pa | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Starfall1969
Frequent Contributor (1K+ posts)
Member # 17353

Icon 1 posted      Profile for Starfall1969     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have those same symptoms.

I've got a definite dx of Ehrlichia and clinical dx of Lyme, babs and bart (waiting for the IgeneX tests).

I'm on Doxy and Rifampin, plus 50,000 IU Vitamin D weekly.

Today was the first day in almost a year I felt mostly decent, except for one episode this afternoon.

Posts: 1682 | From Dillsburg, PA | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
disturbedme
Frequent Contributor (1K+ posts)
Member # 12346

Icon 1 posted      Profile for disturbedme   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sounds like Babesia to me. I have those symptoms as well. The shortness of breath has been MIA or totally toned down for the last couple of months since being on Mepron for almost six months now.

--------------------
One can never consent to creep when one feels an impulse to soar.
~ Helen Keller

My Lyme Story

Posts: 2965 | From Land of Confusion (bitten in KS, moved to PA, now living in MD) | Registered: Jun 2007  |  IP: Logged | Report this post to a Moderator
Tiramisu
LymeNet Contributor
Member # 15082

Icon 1 posted      Profile for Tiramisu     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had episodes of what I think was tachycardia, also rapid breathing. Not actually shortness of breath.

Also palpitations for years.

Just tried Hawthorn Berry Extract a few months ago, and was surprised that it worked.

Don't know if I have any coinfections.

Posts: 175 | From SW PA | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ok the salt/parasite thing looks like a hoax, nice try though. Isn't this board scanned for trolls like this?

http://lymeblog.com/modules.php?name=News&file=article&sid=1242

Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
Toppers
LymeNet Contributor
Member # 20083

Icon 1 posted      Profile for Toppers     Send New Private Message       Edit/Delete Post   Reply With Quote 
And Gael I did a search, you seem to be the only one promoting this salt thing. Hahaha nothing like having a debilitating illness that doctors can't help you with, them internet scammers bombarding you with profiteering websites. I quit.
Posts: 501 | From Cleveland Ohio | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.