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» LymeNet Flash » Questions and Discussion » Medical Questions » I just got out of the Hospital again and Need some Help !!!

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Author Topic: I just got out of the Hospital again and Need some Help !!!
VeryNew2Lyme
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Hey everyone, I just got home and I have to post this question as I truly just need some explanation as to what is happening to me.

I went into the Hospital yesterday because my heart was racing so bad and I couldn't get it down.

I was admitted just on this basis as it is a physical finding, but my other complaints were dismissed as anxiety and depression, but they are 100% real. So I have a few questions if someone can answer them as I know that I am not crazy.

1. My heart doubles in rate when I go from laying down to standing. When I stand up, I feel a rush of adrenaline shoot to my heart each and every time. It feels like anxiety, but it is definitely a rush sensation of adrenaline, like a rocket shooting up the middle of my chest.

I was watching the heart monitor and about 5 seconds after I feel this rush, I see my heart rate climbing and the rate went from 80 to 160 steadily over about 30 seconds and remained at 160 until I layed down. The doctor had no idea of why this was happening and was wondering if you could tell me how a spirochete or bacteria knows when I'm laying down or standing up, as if they had a brain. Or is this the cause of something else ?

2. I complained of weakness in my legs and when I was discharged I had to walk a block to my dads car and up three flights of stairs. I barely made it up the stairs and at the top of the stairs I noticed with each step I took, my legs were rubbing against each other and my feet were criss crossing in front of each other as if I had Cerebral Palsy. I felt like I could use those crutch canes that grasp the wrists for support. This must be exactly what people with CP experience.

I have had this weakness before but never pushed myself to walk such a distance, but today had no choice. Last time this happened, I had most of my strength back the next day. I pray that I get my strength back tomorrow. So, again, I ask, what is this all about ?

3. Lastly, I want to ask a question about my emotions. It seems like I fell like crying quite often, yet I really don't feel depressed at these times. So, I sometimes hold it in and sometime just let it out and say the heck with it. Again, and sorry for all of the questions, but what is this ? I am lost in Lyme and need some insight for my sanity.

Thank you as always, you people are so kind and helpful in putting things into perspective.

Shannon

Posts: 32 | From DC | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
VeryNew2Lyme
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I just found out that #1 about can be known as POTS, which is also known at Dysautonomia Postural Orthostatic Tachycardia Syndrome. Is this part of Lyme or a separate condition in itslef I now have ? Just gets worse and worse.

Shannon

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Leelee
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I am sorry I have no explanations or help for you as I am still learning myself, but I did want to send you hugs and best wishes.

My thoughts are with you.

--------------------
The ultimate measure of a man is not where he stands in moments of comfort and convenience, but where he stands at times of challenge and controversy. Martin Luther King,Jr

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seibertneurolyme
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POTS or othostatic hypertension can be caused by severe adrenal fatigue. It can be caused or worsened by Lyme or other tickborne diseases but this is a medical condition that needs to be treated separately.

The most common treatment is blood pressure meds.

Bea Seibert

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beths
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I had POTS really badly-It went away with treatment and adrenal support
Posts: 1276 | From maryland | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
feelfit
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VNTL,

POTS is often a go along with Lyme. Several here have this condition. It should improve with treatment.

You symptoms are classic POTS.

I have tachycardia too and when it is over I am very weak....never got the leg crossing stuff though, just feel like passing out.

Hope that things improve quickly for you.

Feelfit

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Geneal
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I take florinef for POTs.

Dysautonomia issues are common here.

Hang in there.

I ended up in the ER with a racing heart and air hunger.

I was diagnosed with Generalized Anxiety Disorder.

That, unfortunately, is common here too.

Hope you feel better tomorrow.

I also have Neurally Mediated Hypotension.

Drinking water prior to getting up out of bed helps this.

Hugs,

Geneal

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steve1906
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Hi Shannon,

I hope you start feeling better soon!!!

Just so you know your not crazy I think just about all of us have been to ER at some point.

I thought I was having a heart attack one night and went to the ER. The ER doctor couldn't figure
Out what the hell was wrong with me so he said I want you to spend the night here at the hospital.

They did different rest every hour on the hour and never found anything wrong with me...
In the morning about 4 doctors came in to talk to me and they all said nothing was wrong.

But, the last doc asked me what you are doing here! I told him the ER doctor told me to spend the night.
He said there's nothing wrong with me (and I knew there was nothing wrong with me). I can't tell you what I said to him!!!

That was my first and last visit to the ER. I found out this is as common as it gets with lyme.
I also had the weakness in my legs.

As far as the crying goes...thank god for little favors I don't have that!!!

Hang in there Shannon where all here for you.

Take care,
Steve [Smile]

--------------------
Everything I say is just my opinion!

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bettyg
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many members here have POTS.

glad you are out, but what a bummer walking 3 blocks and up those stairs. have no knowledge on what you are going thru there.


are you on any anti-depressants? i'm on sertraline, can't remember other name; 1/2 pill a day ... sure helps on mood swings, etc.


but crying is good for the system too, so let it out! YOU'LL HAVE LESS WRINKLES!! see, there are a few good things in this mess. [Big Grin] [lol]

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