M
Mozam
Guest
Hey everyone,
Feels like forever since I posted on these boards - too long!
I'd like anyones experience/advice, if possible. At the moment I'm suffering from, and have been for a while apparently, a condition called Achalasia. It's where the muscle at the bottom of your gullet/top of your stomach (the Cardia) doesn't relax sufficiently enough to,let food and drink pass into your belly. It's supposed to be relaxed in order to let food pass through, and closed so that you can't get food refluxing back up again. In my case, it's shut pretty much permanently. Eating therefore, is a nightmare - it's hit and miss as to whether it is all thrown back up again, cos it's got nowhere else to go.
I've now been referred to a surgeon at Edinburgh Royal Infirmary, and they are going to give me a Heller Myotomy - which is where they basically remove the offending muscle. I am absolutely praying to the heavens that this procedure makes a difference and gives me back the ability to eat and drink properly.
I'd like to ask this - does anyone on here suffer from this condition, or has anyone ever had the op I'm talking about? I should note that this condition is apparently not in the SLIGHTEST linked to Crohns - anyone can get it at any time, although it is normally older generations that get it, and it does get progressively worse.
Sorry if I've rambled on a wee bit - I tend to go on a wee bit.
Farewell, from a HELLUVA cold Scotland
Mozam x
Feels like forever since I posted on these boards - too long!
I'd like anyones experience/advice, if possible. At the moment I'm suffering from, and have been for a while apparently, a condition called Achalasia. It's where the muscle at the bottom of your gullet/top of your stomach (the Cardia) doesn't relax sufficiently enough to,let food and drink pass into your belly. It's supposed to be relaxed in order to let food pass through, and closed so that you can't get food refluxing back up again. In my case, it's shut pretty much permanently. Eating therefore, is a nightmare - it's hit and miss as to whether it is all thrown back up again, cos it's got nowhere else to go.
I've now been referred to a surgeon at Edinburgh Royal Infirmary, and they are going to give me a Heller Myotomy - which is where they basically remove the offending muscle. I am absolutely praying to the heavens that this procedure makes a difference and gives me back the ability to eat and drink properly.
I'd like to ask this - does anyone on here suffer from this condition, or has anyone ever had the op I'm talking about? I should note that this condition is apparently not in the SLIGHTEST linked to Crohns - anyone can get it at any time, although it is normally older generations that get it, and it does get progressively worse.
Sorry if I've rambled on a wee bit - I tend to go on a wee bit.
Farewell, from a HELLUVA cold Scotland
Mozam x