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» LymeNet Flash » Questions and Discussion » Medical Questions » Could this be POTS?

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Author Topic: Could this be POTS?
sickntired19
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Has anyone here been diagnosed with POTS or any form of dysautonomia?


So for months I have experienced some weird things but thats the story of Lyme, right?!?
Well, the other night I got up to fill my water bottle, use the bathroom, etc. I had been out of bed for about 5-10 min. when I was standing in front of my bathroom mirror. I felt terrible: nausea, lightheadedness, etc. And all the sudden I realized that my body was just rigid and that I was slowly going backwards.

All the sudden I realized that I was passing out. So I gathered all I had in me and over-corrected and fell on my counter top. I didn't lose consciousness but felt almost like my brain was paralized for a bit.

I stayed there for a bit, I don't really know how long, but long enough that I thought I would be fine. When I stood up everything just started to go crazy. Horrible nausea, headache, lightheadedness, etc. But all the sudden my inner ear felt like it went frozen, so so cold. Then my brain felt frozen. All the sudden I realized that I AM going to pass out, I have to get to my bed.

I know I know, duh, right?!
So I started to walk to my bedroom but only got to the bathroom door (maybe 3 steps) when my arms went freezing cold, and I knew that I was never going to make it to my bed.

I started to lower myself to the floor but before I could, I fell and passed out. It seemed for only a slight second, however I really don't know. I just layed there for what seemed like maybe 3 minutes but was really about 30. I finally made it back to my bed, I didn't want my brother-in-law to come out in the morning and find me half dressed in the hallway!!

So I was thinking what could be going on? All during the night I had been slightly lightheaded, nauseated, and my nerves were so "jumpy". Every time I even swallowed, my nerves jumped.

I remembered seeing a video about Dysautonomia on youtube and thought I should look into it. These are the symptoms that I have:
lightheadedness, sometimes called pre-syncope (pre-fainting) dizziness (but not vertigo, which is also called dizziness)[4]
exercise intolerance
extreme fatigue
syncope (fainting)
cold extremities
chest pain and discomfort
disorientation
tinnitus
dyspnea
headache
muscle weakness
visual disturbances
abdominal pain or discomfort
bloating[5]
constipation
diarrhea
nausea
vomiting
brain fog
burnout
decreased mental stamina
depression
difficulty finding the right word
impaired concentration
sleep disorders
chills
feelings of fear
flushing
overheating
nervousness
over-stimulation
The only other symptom that they listed was excessive thirst, and I definitely don't have that.

What I don't understand though is that I thought all of these things were Lyme symptoms. So can this really be POTS or is it just Lyme?

I know the last 10 years, I can't stand still for long without feeling like I am going to pass out, and my feet get all red and blotchy and itchy. When I get up from a sitting or laying position, I get lightheaded, have visual issues, loose my balance, my heart just pounds, and sometimes I feel like I am just going to pass out.

Until now I never gave POTS much thought since I hadn't pass out.

So what do you guys think??

Posts: 265 | From Oregon | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
beths
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You can have POTS without passing out. I had it badly, check tour heart rate when standing. Mine would jump to over 120.
Posts: 1276 | From maryland | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
sickntired19
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I have and often when it just feels out of control it is around 120-140.
Posts: 265 | From Oregon | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
lululymemom
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It does sound like POTS to me.. My daughter had it. It did go away with Babesia treatment..

--------------------
IGM 41 IND, 83-93+ IGG 31 IND,34 IND, 41++, 58+, 83-93 IND

31 Epitope test neg.

Bartonella henselae 1:100

Posts: 2027 | From British Columbia | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
sickntired19
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Up
Posts: 265 | From Oregon | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
BoxerMom
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POTS is common in Lyme. Very common. It gets better with treatment.

I agree that the infection that seems to make it the worst is Babesia.

--------------------
 - Must...find...BRAIN!!!

Posts: 2867 | From Pacific NW | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
sickntired19
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Ok, so I have been on Malarone for just over 2 weeks.

Well, I treated for stupid little stints a couple of months ago but whatever

Anyway, so do you think that the worsening of the POTS symptoms might be a herx reaction?

Posts: 265 | From Oregon | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
   

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