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» LymeNet Flash » Questions and Discussion » Medical Questions » Severe muscle spasm nearly caused asphysixation. What do I do?

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Author Topic: Severe muscle spasm nearly caused asphysixation. What do I do?
Robert is king
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Hey everyone,

Last night I had a very severe muscle spasm. The muscles in my arms, legs, and chest all went into a severe spasm and I was unable to get them under control. This has happened before, but last night was different. I could barely breathe this time. The muscles in my chest were so tight I just couldn't get any air in. I'm 19 and live at home and it took over a full minute before I could get enough air to call my parents downstairs. I was so scared I felt like I was going to die. Eventually it stopped on its own. What should I do in this situation? My parents hate the ER, but it really seems like this is one time I should have gone. Does anyone have any ideas about what I should do if this happens again?

[This message has been edited by Robert is king (edited 06 December 2004).]


Posts: 58 | From Palo Alto, CA, U.S.A. | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
TheCrimeOfLyme
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Go to the ER


Posts: 3169 | From Greensburg, Pennsylvania | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
nan
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To the ER......definitely!! Sounds scarey, Robert. Hope it won't happen again.
Posts: 2135 | From Tick Country | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
riversinger
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Call your doctor, find out what they recommend. Something like Ativan may be a possibility, but you need medical advice.

If it happens again, definitely go to the ER!

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Sonoma County Lyme Support
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Posts: 2142 | From California | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
can not remeber
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Ativan...

Anyone know the symbol? We could become wealthy from this epidemic disease and the pharm co.
Unfortunatley, i must rely upon it more and more for sleep and siezure control.
What the hell happened - it was a bug bite for crying out loud.


Posts: 61 | From cosmo | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
algr
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I haven't had anything that acutely scary happen to me yet so I'm not sure what to suggest but I just had to say I know how you feel in this general Lyme boat...I am 19 too and I live with my mom and commute to college classes (hopefully I can keep that up).

It's really hard to be so young and have these scary things happen to you, but luckily our youth will help us heal as fast as possible.

Take care of yourself!

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cheers,
AG


Posts: 119 | From NJ, USA | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
jo3
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Hi Robert,
I had a very similar experience a week ago. I was cleaning my shower stall with Clorox (the idustrial one) and not 2 minutes wnet by when I started coughing uncontrollably. It just kept getting worse and then I felt my lungs expanded as if they were going to explode. I then started wheezing and gasping for breath- I, like you, thought I was gonna die. It took me a few minutes to catch my breath and then I was quite sore and shaken-up afterwards. I didn't have enough time to think about the ER- I had to try and save myself in front of my 2 teenagers- all I kept thinking was that this was a terrible way to die. Thank God, it was very cold outside and the air really opened up my lungs- but what a scary feeling,especially at your age.I don't think I would of made it had I of not gone outside- much less the ER.
All I can say is the cold air helped me- maybe breathing into a paper bag would help.
I know this totally stinks- some days you feel pretty good and others you feel like you've been hit by a truck. Hopefully, your Dr. is working real hard to get you healthy again.
Hang in there- come to this board whenever you need advice or someone to talk to-there's lots of good people around.

Posts: 247 | From san antonio,tx | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
riversinger
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Raskilnokov, Robert is not talking about going to the ER to get treated for Lyme. Robert already sees a doctor for Lyme treatment. He is talking about going because he has a life threatening symptom that needs to be managed immediately.

The ER is not good for treatment of on ongoing, chronic condition. It IS the place to go when you need immediate intervention.


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Sonoma County Lyme Support
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Robert is king
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Thanks everyone for the replies. It happened again last night, but fortunately this time I was able to breathe. And yes I am seeing a LLMD for treatment. I'm still shaken up about this whole thing, but I think I'll be okay.
Posts: 58 | From Palo Alto, CA, U.S.A. | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
riversinger
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Robert, have you been able to reach your LLMD? Sounds like you need an intervention on hand.

Glad at least this last one you were able to breathe.

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Sonoma County Lyme Support
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Robert is king
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Riversinger, I haven't been able to get a hold of him yet. He's always very overwhelmed and difficult to contact. I'll keep trying though.
Posts: 58 | From Palo Alto, CA, U.S.A. | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
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Robert,

My husband has these types of episodes multiple times daily for last year or two. The only thing that works for him is IV Ativan thru his PICC line -- 1/2 or 1 mg usually does the trick. I still have to manually move all his muscles for 10 - 15 minutes to get everything to relax.

If this is a new symptom, possibly IV magnesium may help. It does seem to lessen the frequency of these episodes for my husband, but he often has these episodes when I am giving him his IV magnesium -- especially if I let the drip go too fast.

Steve usually starts coughing then has dry heaves and then shakes all over like a seizure before he freezes up. I call it transient quadriplegia.

Often his jaw locks up so he can't speak to call me. We would really be in trouble if he didn't have the coughing and heaving to alert me if I am in the other room.

The other thing that helps him is his CPAP machine. He puts that on because the shaking sometimes makes him hyperventilate.

It is soooo hard to say, but Steve's Dr's seem to think these "seizure-like" episodes may be caused by Babesia. Have you been tested or treated for that?

Steve's episodes are usually caused by some trigger event. Try to remember if something happened to cause these episodes.

The triggers for my husband are sudden loud noises -- telephones, a knock on the door etc. -- eating, waking up from sleep, initiating movement, or even talking on the phone too long. Moving the diaphragm seems to be a big part of the problem for Steve.

Please let me know what your LLMD says and if you find anythig to help with this symptom.

Bea Seibert

[This message has been edited by seibertneurolyme (edited 07 December 2004).]


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Robert is king
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Bea,

Yes, I have been treated for Babesia. I've been retested and it came up negative, but who knows? I suppose it may be possible there's still some in there.

This isn't exactly a new symptom. It's happened off and on for several years. It's the lack of oxygen that's new. I don't have a PICC line in so IV Ativan could be tough to administer. I'll keep trying to get a hold of my doctor.

As for the cost of an ER visit I'm glad to say that wouldn't likely be an issue. My insurance has been unbelieveable. They've covered everything I've needed. Even if they didn't cover a trip to the ER my family has the money needed to cover it.

Thanks everyone for all the replies.


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seibertneurolyme
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Robert,

Ativan or Lorazepam for injection can be used either IV or IM (intramuscular shot).

I have never given Steve shots, but this might be an option for you.

I have to keep syringes filled and ready to go for my husband and carry a cooler with us everywhere we go.

The only bad thing about Ativan is that it is a benzodiazepine and this class of drugs are addictive. Valium or Diazepam is a milder benzo and Klonopin or Clonazepam (another benzo)is also sometimes prescribed for tremors/myoclonus.

This is probably my husband's most disabling symptom and we are really frustrated with his Dr's who don't know what else to do besides IV Ativan. We are constantly in crisis mode as he has an average of 4 - 6 episodes daily.

If your problem is becoming more frequent I would be concerned about either progression of the Lyme or other coinfections or a herx reaction.

For my husband a good day is a 2 mg day, but unfortunately lately he has been requiring 3 - 4 1/2 mg IV Ativan daily. After the IV Rocephin (so far the only drug which has done him any good) he got the IV Ativan down to 1 mg daily for a very short time, but things have been pretty much downhill ever since.

My husband even has these "seizure-like" episodes in his sleep and his grunting and gasping for breath will wake me up and I will find him frozen up with all his muscles locked up and unable to move or speak.

I don't want to scare you, but based upon my experiences with my husband I think you really need to try to get to the bottom of this -- something we have never really been able to do unfortunately.

Bea Seibert


Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
   

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