Achalasia, Biopsies and Diabetes
Posted , 4 users are following.
Hi All
I haven't been diagnosed with Achalasia, but a lot of the symptoms I have read makes me think I may have this. I have been suffering for ages, the last 20 years ish, but it has worsened the last few years. I have been for an endoscopy last week, they said my lower and middle oesophagus have been narrowed, and they have taken biopsies. I am just hoping I have some positive results as it would give me a piece of mind to know that I might have achalasia or something similar, I am tired of not having a solution.
Questions I have:
How long does it take for results of a biopsy to come back?
Do they classify achalasia as something urgent?
How will they let me know I have this or something similar?
I have been under the care of Dr Curtis (King's Colleges and Princess Royal Hospital in Orpington). Does anyone know if he is good?
I only heard this from my cousin who is about to qualify as a Dr in the next couple of months, not from any other Dr or specialist.
I feel very scared right now, as I only deal with the regurgitation at home or in a restaurant. I'm a teacher and I'm worried that the school will not understand/be accomodating. I feel this situation is getting worse and this happens with a lot of foods I eat, and it is getting frustrating. I'm also already petite, and feel like I constantly can't keep the weight on, despite having underactive thyroid, neither type 1/2 diabetes (not officially either, unofficially type 2), and my 'allergies,' are getting worse.
Any suggestions would be great!
I really appreciate any help that could be given.
Thank you in advance.
Asha
0 likes, 4 replies
quantumq4 asha28860
Posted
Hi Asha,
They only take a biopsi 'cos they are in there anyway........
It sounds like Achalasia.
The results 'should' be with your doc in a week, or 2 weeks at the most. Your next test will be a 'pressure test' , I can't remember what it's called but I think it measures how much 'spring' your food pipe has (that's how I thought of it anyway).
The result will be either yes or no for Achalasia.
You 'should' then be automaticly referred to an Upper GI specialist. I'm under Dr Banks at UCLH in Euston Road London. His team are brilliant.
Good luck.
Chris
neil32387 asha28860
Posted
Understanding your condition will likely take a while, and you will have lots of options to consider if it is Achalasia. I think the Manometry (pressure test) is considered to be definitive re a result. I personally found the test to be painless but a bit weird; for me it was nothing compared to Endoscopy. It basically shows the strength and profile of muscles when swallowing. Accuracy/strength of contractions to move food if you like. I think it might be possible to have temporary muscle malfunctions, but if swallowing problems (lack of peristalsis) are persistent over months or years then Achalasia will likely be the conclusion... Most people with A get worse with stress and anxiety, so best try and stay calm and happy
(easy to say I know); maybe spend some time doing what you enjoy best... I go fishing or taking photos..
This group is great to air and share, so friends wont be far away as your picture starts to become clearer.. In the interim, I find that Magnesium and VB can really help (both high strength), and drinking warm water followed by a gentle cough. Raising an arm whilst swallowing can help me too... Notwithstanding a hot tub!
some positives at least
...
Warmest, Neil
Nettie_Noo_Noo asha28860
Posted
Nettie_Noo_Noo asha28860
Posted