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Re: Diaphragm spasm?

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Unfortunately, all I can advise is to keep drinking water, or try eating

something. I tend to have this happen when I have gas sitting somewhere,

and once it finally moves, the pain from the spasms will stop.

On Tue, Feb 1, 2011 at 11:39 AM, <kcamitta@...> wrote:

>

>

> For the 1st time I am getting spasms that seem to be at the center of my

> diaphragm. It has been going on for about 30 minutes. They are about 30

> seconds apart & last just a few seconds. With regular esophageal spasms

> drinking cold water helps me. Not working here.

>

> I had my myotomy 2 years ago.

>

> Anyone had this experience? If you have, any tips for making it go away?

>

> At work & want it to go away!!

>

> Thanks

> Kathy

>

>

>

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All I can think of is Maalox. Don't let yourself get too hungry and certainly

don't overeat. I find those two things combined with stress prompts mine.

Donna Hall

>

> For the 1st time I am getting spasms that seem to be at the center of my

diaphragm. It has been going on for about 30 minutes. They are about 30

seconds apart & last just a few seconds. With regular esophageal spasms

drinking cold water helps me. Not working here.

>

> I had my myotomy 2 years ago.

>

> Anyone had this experience? If you have, any tips for making it go away?

>

> At work & want it to go away!!

>

> Thanks

> Kathy

>

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Hi all!

haven't posted in a while but read daily. diagnosed 2008, Heller/Dor 11/2008.

things have been ok, much better after surgery. gained 25 lbs back ( not too

happy about that, but in grand scheme shows dramatic improvement) in december

had an episode of horrible epigastric pain for about 5 days. ended up at ER,

dillaudid for the pain. off to Boston I go.. local hospital has no understanding

of our condition. due to family history of pancreatic cancer a CT scan is done.

CT shows enlargement of retrocrural lymph nodes. Doctor explains that these

lymph nodes are near the diaphragm! Imagine my surprise when I see this post!

have noticed increased spasms and difficulty swallowing again, things go through

but really feeling things " hanging up " and taking longer to go through. Anyone

feel that this is related? Looking forward to some insight from this fabulous

group! Thanks from Mass

>

> For the 1st time I am getting spasms that seem to be at the center of my

diaphragm. It has been going on for about 30 minutes. They are about 30

seconds apart & last just a few seconds. With regular esophageal spasms

drinking cold water helps me. Not working here.

>

> I had my myotomy 2 years ago.

>

> Anyone had this experience? If you have, any tips for making it go away?

>

> At work & want it to go away!!

>

> Thanks

> Kathy

>

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Notan: your knowledge so amazes me! I was so hoping you would respond to this

post. The CT scan showed mild enlargement and suggested a 6 month follow up. I

have a CT scan then an upper GI the following week. this will take place in

June. If I remember correctly when I had my mannometry there was something with

the LES pressure not being consistent with a typical Achalsia patient. My

symptoms had actually progressed and worsened pretty quickly, from late June to

finally surgery in November after a 40 lb weight loss. I too am quite interested

to see how this all coincides.

> > ... CT shows enlargement of retrocrural lymph nodes. Doctor explains that

these lymph nodes are near the diaphragm! ...

>

> Those nodes would be behind the crura of the diaphragm, between

> diaphragm and the spine in the retrocrural space. That is where the

> aorta is. The right crus and left crus come off the spine and cross on

> the other side of the aorta and then cross again around the esophagus

> forming the hiatus where the esophagus goes through the diaphragm. The

> crural diaphragm there also contributes to the pressure of at the LES

> and so even breathing changes the pressure at the LES.

>

> It isn't a big jump from the esophagus and the retrocrural lymph nodes.

> I don't know much about how the lymph system is connected to the organs

> but I would guess that retrocrural lymph nodes have connections to the

> esophagus. Did they say anything about the enlargement of them? Will

> they follow up on it? If not, I would bring it up with your PCP and see

> if he has an interest in it.

>

> Others have notice that their achalasia symptoms change with changes in

> their bodies, pregnancy, stress and such. Those lymph nodes may indicate

> that something is happening in your body possibly at or near your

> esophagus. It may or may not be connected to your symptoms.

>

> When I was a baby I had mono. All through my childhood I had swollen

> lymph nodes on my neck. I was told it was left over from the mono I had.

> Who knows.

>

> notan

>

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