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>I have been short of breath frequently, even while just sitting. I just

feel like I am not getting enough air. I will suddenly need a fast, deep

breath. I have also had this gut feeling (which have been very reliable in

the past) about this breathing problem and have this great fear that I will

have trouble breathing. >>

Your respiratory system is not doing everything that it normally does

automatically. You feel like you have to " remember to breathe " , right ?

This is evidence of brainstem compression and isn't to be taken lightly. I

had the same problem, and it got worse quickly (weeks). See your

neurologist or whoever is orchestrating your care, soon.

Respiratory failure is one of the most serious symptoms that an ACM patient

can suffer from.

Chip

" Breathing isn't optional " -Respiratory Therapist @ Abbott

Northwestern Hospital in Minneapolis

=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=

E-mail: chip@... (ACM-1, 28 months post-op)

St Croix Beach, Minnesota

Home page: Http://www.pressenter.com/~chip/chiari.htm

=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=

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In a message dated 3/8/99 9:25:39 PM Eastern Standard Time, scrow@...

writes:

<<

I have been short of breath frequently, even while just sitting. I just feel

like I am not getting enough air. I will suddenly need a fast, deep breath. I

have also had this gut feeling (which have been very reliable in the past)

about this breathing problem and have this great fear that I will have trouble

breathing.

If anyone has any similar problems or knows what this is all about I would

appreciate it if you could email me. Thanks! , scrow@...

>>

Hi ,

I had this before my surgery in December 98. Just like you, I could be

sitting there and just start gasping. For me, it was nothing but the old

chiari. I would pant just walking out to the car, through the house, or even

sometimes if I just said too long of a sentence.

This was one of my symptoms that went away immediately after surgery. I still

get short winded easily, but at least it's not when I'm sitting down doing

nothing. Stairs kill me, but now it's probably from being just plain old out

of shape. After 6 months of being down and out with all this $!@*, my body is

screaming for physical activity. I still can't walk more than 1 1/2 miles,

but oh well...

Hang in there. BREATHE!!

Tina

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In a message dated 3/8/99 10:52:55 PM Eastern Standard Time,

chip@... writes:

<< Your respiratory system is not doing everything that it normally does

automatically. You feel like you have to " remember to breathe " , right ? >>

I have had this problem on and off for about five years. Just when i can't

stand it anymore it eases up again. I find that it has to do with how much i

do with my arms. Using my arms and upper body tends to fatigue my muscles and

that extends down to the ones that control breathing. Also i acknowledge that

it has to do with pressure on the brainstem too.

Lately i have had alot of pain and pressure in my head. and it gets worse

when i lay down and try to go to sleep. I see my nsg again on the 26th and

will have to talk to him about it. I really don't want to go for surgery. am

hoping maybe we can try some new meds to ease this off for a while.

Terri in NH

ACM1 and MS

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has always had breathing problems. After the decompression surgery they

would ask him to blow in the breathing machine and he would throw up

everytime. Did anyone else have this problem?

Sherry

Mother of

decompressed 10/21/98

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To All,

Shortness of breath isn't nessarily related to ACM, in my case it is

related to the stroke. If someone has had a stroke which has ended in

paralysis then the muscle's around the lungs will begin to shrink. The

shortness of breath in people with just ACM occurs because the chiari is

putting pressure on the nerves that control breathing. Correct me if I'm wrong

Chip or Ronny.

June

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Original Article: /list/chiari/?start=13650

> Hi Everyone,

>

> I am a little scared because I have been having shortness of breath/pulmonary

problems. They have been getting worse. I have Chiari 1, 8mm,no surgery.

>

> I spent the morning getting tested in the pulmonary unit at the hospital.

Having to quickly inhale as much as I could and then blow out as hard and as

long as possible, while the technician goaded me on, was like having a migraine

every eight minutes. It was not pleasant to say the least. The technician said

that things weren't " normal " but didn't say what or how mild or severe they

were. She also had never heard of Chiari (shock) so she said my Doc would have

to explain how my results were related to Chiari.

>

> I have been short of breath frequently, even while just sitting. I just feel

like I am not getting enough air. I will suddenly need a fast, deep breath. I

have also had this gut feeling (which have been very reliable in the past) about

this breathing problem and have this great fear that I will have trouble

breathing.

>

> If anyone has any similar problems or knows what this is all about I would

appreciate it if you could email me. Thanks! , scrow@...

> Hi , I too get short of breath. I guess it is my brain stem

irritation from chiari. Plus, My blood pressure will swing on both ends. Either

I will be very low blood pressure or high blood pressure. I also wonder if this

is related to ACM. I am seeing a neurosurgeon. He is considering if my case

warrants decompression surgery.

They still think my symptoms are possibly MS but if they would just read ACM

disease profile I think they would see this closely matchs what I experience on

a daily basis.

Best of Luck, Take Care Ann Reitz

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