Jump to content
RemedySpot.com

Re:

Rate this topic


Guest guest

Recommended Posts

Hello from Elena! I've had achalasia for 3 years now, first doctors thought

I was crazy, then I had two botox injections, then a dilation. Just three

weeks ago I had a Heller's Myotomy. It's too early to say whether I'm cured

but I am much better. If you'd like, e-mail me for more info.

Link to comment
Share on other sites

Hello : My name is Elena and I've had the dilation. You receive a

sedative then the doctor inserts an endescopic camera and performs the

dilation through the same device that houses the camera. The team at UCLA

was very professional and let me look at all the equipment and ask all kinds

of questions. The dilation gave me the most relief (as opposed to the Botox

injections). For some people it's the other way around. Unfortunately, my

symptoms got worse because I had the achalasia for a long time. Three weeks

ago I had a Heller's myotomy. If you'd like, I'll forward some med sites to

you for review. Let me know if you'd like any more info personally. Wishing

you a successful dilation, Sincerely, Elena Wagner

Link to comment
Share on other sites

Hi! I had two dilations. The first was using the guide wires to do the

procedure, and I had no relief at all. The second was using a balloon

device, and I experienced problem free swallowing for 2 days. After

that the symptoms of achalasia started to return slowly. I had a little

soreness and irritation in my throat for a day or two, and experienced

SEVERE heartburn after the last dilation. I had a Heller Myotomy last

Monday, am still recovering. During the procedure, the surgeon found

small leaks in my esophagus and that may have been the cause of the

heartburn. It is hard to say for sure. Good luck, and I hope this

gives you some relief!

howard@... wrote:

>

> I am about to go in for a dilation, and would like to know what others

> have experienced.

>

> ------------------------------------------------------------------------

> Imagine a credit card with a 0% Intro APR and Instant Approval…

> It seems impossible, but it’s not. Visit GetSmart.com’s Credit Card

> Finder and click on instant approval cards right now at

> http://clickhere./click/1269

>

> -- Easily schedule meetings and events using the group calendar!

> -- cal?listname=achalasia & m=1

Link to comment
Share on other sites

Hello,

They actually went in and cut the esophogus where it was pinched off and it

really helped. I guess the muscles will never work again but I am able to

live with it now and I do sleep at night. When the did the barrium swallow

on me it was taking a whole day for the stuff to get to my stomach.

The Cleveland Clinic is a wonderful place for this problem. They specialize

is this surgery. I will look and see if I can find the link that tells about

the surgery.

You did not say where you were from so I don't know if Cleveland is an option

for you.

He told me they could do the balloon but it probably would just be a temp.

fix.

Let me know what you think.

Mark~

Link to comment
Share on other sites

Hi everyone, I'm a little surprised your doctor told you that dilation can be

done as many times as necessary. My understanding of the procedure is that

each dilation becomes less effective. Have you considered a botox injection

instead? E

Link to comment
Share on other sites

Hello - I had the Heller's myotomy on 10/20/99. The articles you forwarded

me suggest the surgery " as easy as one-two-three " . My surgery was three

hours long and I stayed in the hospital for three days. I wouldn't

catogarize it as easy. I feel better but not 100% and have reflux now. At

least I can sleep now without waking up choking. This surgery is not for

everyone and anyone considering it should discuss it thoroughly with their

doctor.

Link to comment
Share on other sites

Hey,

Sorry I made you think it was easy. It was the toughest thing I ever went

through in my life. My surgery was 5 hours long but I was to the point that I

could not go on the way things were.

Mark~

Link to comment
Share on other sites

I think the problems started again because I did not follow my diet. It

started again after about 3 months but nothing like before the surgery. I

still sleep at night and I think I have learned to eat better.

Mark~

Link to comment
Share on other sites

Hi Mark - the articles made it sound easy, I KNOW it's really hard. How are

you recovering? I wasn't allowed to drive for two weeks following the

surgery. It was hard to stay still but somehow I made it through OK.

Link to comment
Share on other sites

  • 9 months later...

Hello . I am sorry to hear that the myotomy did not help. How

long ago did you have it done? Have you tried the botox injection?

Maybe nifedipine or nitroglycerine tablets can help. What has your

doctor told you? I can understand how you can feel depressed with

this disease. Sharing with this group can help.

Alan

Link to comment
Share on other sites

My husband,

has had two failed myotimies; Nitro does not help his attacks!!! Carol if

you are listening; Please help us, I 've gone as far as to try to find cola

syrup. The only thing that i could find that the pharmacist said was cola

syrup was red. The directions for use was as a laxative. I live in North

Bay, Ontario. Ask anybody the doctor's up here are os!!! Believe most

other professionals agree with me entirely. The syrup i obtained was red,

and i was assured it was the same thing as cola syrup. I do not believe that

this was the right medicine for my husband!!!!

Please reply,

The drepression and no help is extremely depressive, I always that that cola

syrup was black! Please advise me if I'm wrong!!! In North bay no other

drug store claims to carry it. If I donot have the right syrup; would a

heath alternative store have it

???

Need an answer ASAP

We desperaately need HELP!!!!

LOVE LAURA

Link to comment
Share on other sites

hello allan thanks for emailing me back i had the surgery about 4 months ago

sept. 10th will be 4 months i talked to my doctor tuesday after having a

hard time swallowing water it would not go down everthing came up i did not

get anything down that day that was this monday he put me on levsin and it

dont seem to help he said if it did not he wants to see me in his office

again and i am going to prevent that if i can they have done two dilations

and stretches it did not help so they did the hellers myotomy on me other

people say that after they have had that they can eat like a normal person

and some say that it was a failure or the symtoms came back after a while i

well i cant eat fruits, bread, meat or anything thats hard i am drinking my

food and eating baby food i have lost some more weight since my surgery the

doctor was talking about more test what would that be? i do not want that

manometry done again it took for ever to get the tube down i am in that

egroups but i cant remember my password please write back and thank you for

emailing me back patricia

Re: achalasia

> Hello . I am sorry to hear that the myotomy did not help. How

> long ago did you have it done? Have you tried the botox injection?

> Maybe nifedipine or nitroglycerine tablets can help. What has your

> doctor told you? I can understand how you can feel depressed with

> this disease. Sharing with this group can help.

>

> Alan

>

>

>

>

>

>

>

Link to comment
Share on other sites

-

The basic difference between the two achalasias is that, with vigorous achalasia, you have painful muscle spasms of the esophageal muscles. These are often described as being similar to those one must feel when experiencing angina or other cardiac conditions. Indeed, many achalasia sufferers delay receiving proper identification of their condition as physicians seek out cardiac causes for the source of the pain. The spasms can last anywhere from seconds to hours and can occur anytime, even waking you out of a sound sleep. There is a prescription drug, Levsin, which is effective in alleviating the pain.

Hope this helps -

Carol

achalasia

hello my name is patricia and i was wondering what is the difference between achalasia and the vigorous achalasia? patricia

Link to comment
Share on other sites

Dear Carol,

now that you have sent a message to about the difference between two

types of achalasia. You have just diagnosed My Husband. He has to have

vigourous achalasia, and I am printing this and taking to Toronto to the new

Specialist. Wish us luck

Thanks so very much,

Link to comment
Share on other sites

-

You might also want to arm yourself with Dr. Zucker's excellent article on

achalasia which can be found at the web site:

http://www.aalaparoscopic-surgery.com/achalasi.htm. This is probably the

most complete document on achalasia I've ever read and discussed all the

diagnostic procedures as well as treatment options. Good luck - let us know

what happens!

I'll be thinking of you!

Carol

Re: achalasia

>

> Dear Carol,

>

> now that you have sent a message to about the difference between

two

> types of achalasia. You have just diagnosed My Husband. He has to have

> vigourous achalasia, and I am printing this and taking to Toronto to the

new

> Specialist. Wish us luck

>

> Thanks so very much,

>

>

>

>

>

>

>

>

_____NetZero Free Internet Access and Email______

http://www.netzero.net/download/index.html

Link to comment
Share on other sites

:

Glad to hear you are going for a second opinion in Toronto! There

ARE specialists in this stuff. I spoke with a doc in Chicago who had

seen approximately 1000 patients suffering from achalasia over the

course of his career.

Hope you find someone like that.

Good luck!

Swack

In achalasiaegroups, red57kw05@a... wrote:

> Dear Carol,

>

> now that you have sent a message to about the difference

between two

> types of achalasia. You have just diagnosed My Husband. He has to

have

> vigourous achalasia, and I am printing this and taking to Toronto

to the new

> Specialist. Wish us luck

>

> Thanks so very much,

>

>

Link to comment
Share on other sites

  • 1 month later...

Abby -

This was a wonderful - if you can use that word! - description of what lies

ahead for achalasiacs. I hope none of us ever get to that point, but we

just never know what will happen. And yes, while I am remarkably improved

to the point where I hardly think of having an eating problem, I do still

have some episodes. When I'm tired or stressed, I'm more prone to the

painful chest spasms. Thankfully, there is Levsin to help ease the attack

very quickly. However, I never go anywhere without an emergency supply -

including my early morning 4 mile walks - so it's always " with me " , in the

back of my mind, that this is a condition I have to live with. Likewise

with eating - I still avoid certain foods, especially when I'm eating out.

If I think there's a chance I'll have something stick, I go for the safe

stuff - like soups or soft foods. Luckily, I like mashed potatoes! My

doctors told me I'd never be 100% and so I'm not upset when these things

happen. On balance, I'm better off that I used to be and for that I'm

grateful.

Your information was well presented and much needed on this site. Thanks!

Carol

achalasia

> :

> Your Dr. didn't tell you what the long term effects of achalasia

> are because he/she probably doesn't know.

> I've had achalasia for four years now. I've had two surgeries to

> correct the problem . Although I'm not perfect, I'm substantially

> better than I was. Of all of us in the group, Carol seems to have had

> the best luck. She doesn't seem to have any residual effects of the

> disease. I,on the other hand can eat much better since my

> surgeries,however I am sttll very aware of the fact that I have a

> disorder that effects my eating.

> No one has told me what to expect except for a cardio-thoracic

> surgeon,who was supposed to perform an esophagectomy(removal of the

> esophagus) on me with my general surgeon. He told me I don't need the

> surgery yet, as I am still able to eat,but at sometime,10,20,maybe 30

> yrs from now I will need one. Most people with achalasia will need one

> at some point ,as this is a progressive disease. Myotomy

> surgery(cutting of the esophgeal muscle) will make you feel better,but

> it is not a cure for the disease.

> When,you might ask does one know when he/she needs an

> esophagectomy? When the esophagus becomes twisted and contorted,due to

> a lack of mobility and usage. The esohagus is a muscle,and as with any

> muscle,if it is not used it becomes flaccid and lax. It may then begin

> to fold on itself making eating virtually impossible. If the Dr. can't

> pass a scope because of the twisting,it's time for an esophagectomy.

> It is possible to live without an esohagus. The surgery can be doe

> two ways. Either part of ypur intestine is used to fashion a new

> esohagus(colan intraposition),or the stomach is puled up into the chest

> and connected to the nub of the esohagus that's left in place. Sounds

> horrible,I know,but peope who have had it done seem to come out

> A-OK.Abby

>

>

>

>

>

>

>

>

>

>

>

>

_______________________________________________

Why pay for something you could get for free?

NetZero provides FREE Internet Access and Email

http://www.netzero.net/download/index.html

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...