Regarding Achalasia
Posted , 3 users are following.
I want to mention again a small group of Achalasians that meet monthly for a chat regarding our condition of Achalasia. We meet in London and if anyone with the condition wants some support, advice or just to speak to others who can understand please message me for more information .
Emis Moderator comment: I have removed the email address as we do not publish these. Please use the message service if you want the information.
0 likes, 9 replies
mark235
Posted
janski
Posted
If you google and join the Meet Up groups forum you will see us all there and you can join and see when we will get together next.
We meet at the Marriot Hotel in Park Lane usually at 2pm on a Sunday.
Sorry to hear about your diagnosis, but we are an elite and rare bunch!!
regards
Janski.
mark235
Posted
mark235
Posted
janski
Posted
We are seperate from this site. If you google Meet Up groups you will find us and you can join.
Our next meet is the 20th October.
Hope you are feeling ok.
Jan
Guest
Posted
virginia20
Posted
I am so glad that I found this site. I have read some stories and feel better knowing that I am not on my own. I was diagnosed with Achalasia two years ago and would love to meet people with the same condition. Do I need to register enable to join the group.
Many thanks
Virginia
janski
Posted
Yes if you google neetup groups and then join you will find our group under Achalasia . It woud e good to meet you at our next meetup in October.
Remember, you are not alone with this condition .
Regards,
Jan x
virginia20
Posted
Thanks for your reply, I would love to meet other people and share my experience.
Virginia x