Welcome to the UK Potsies...
UK Potsies is a campaign and organisation dedicated to raising Postural Orthostatic Tachycardia Syndrome awareness in the UK.
Following people from the UK living with P.O.T.S - a form of Dysautonomia,
to raise awareness and reach out to other victims of P.O.T.S and Dysautonomia.
"Through our YouTube channel and blogs we are sharing our journey - with this chronic illness - with you."
UK Potsies also provide an online haven for other P.O.T.S sufferers - or anyone who may be closely affected - to come together for help, support and raising awareness. Together we are doing all we can to spread the word about this rare and chronic illness while helping sufferers at the same time.
Our motto: "P.O.T.S - Life can still blossom!"
Following people from the UK living with P.O.T.S - a form of Dysautonomia,
to raise awareness and reach out to other victims of P.O.T.S and Dysautonomia.
"Through our YouTube channel and blogs we are sharing our journey - with this chronic illness - with you."
UK Potsies also provide an online haven for other P.O.T.S sufferers - or anyone who may be closely affected - to come together for help, support and raising awareness. Together we are doing all we can to spread the word about this rare and chronic illness while helping sufferers at the same time.
Our motto: "P.O.T.S - Life can still blossom!"
Meet the team:
Some of you may
already know us from our UK Potsies YouTube channel and we want to thank
you for coming to take a peek at our website. We hope you will become
regular visitors and that we can get to know all you potsies out there
(there are more of us than we think!).
If you are new to us then let's introduce ourselves:
We are Marcia, Tara, Liz, Rebecca, Liam, Olivia and Laura. We also have amazing people working behind the scenes of UK Potsies like Eve and Kathy.
Marcia founded the UKpotsies in February (2011). The first person she approached to join was Tara (Co-founder) as she was one of the only people she had met with P.O.T.S. Tara was instantly enthusiastic and got on board the other lovely ladies Liz, Rebecca and Laura who all do so much to contribute to various POTS projects and the UKpotsies.
Later on Liam found us and joined the team giving a much valued and needed male perspective on living life with P.O.T.S. Olivia also joined the UK Potsies as a great contribution for teenagers and young people suffering with P.O.T.S.
Now we have the most wonderful group of people working in front of cameras and behind the scenes, each person doing a tremendous amount to contribute to this non-profit awareness organisation.
We have each been on our own little journey of ups and downs with P.O.T.S and learned a great deal that we want to share with you, in the hopes that we can stand together as a united community to help patients and families and raise awareness at the same time. Our main aim is to be a friendly, happy group that offers emotional support and reaches out a friendly, helping hand to fellow P.O.T.S sufferers across the UK- and the world.
For more help or information, speak to your doctors and specialists for medical support and advice.Please be aware that any advice provided here should not replace the knowledge or help of your medical professional, and should merely act as a reminder of possible things which may help.
Please see our disclaimer.
If you are new to us then let's introduce ourselves:
We are Marcia, Tara, Liz, Rebecca, Liam, Olivia and Laura. We also have amazing people working behind the scenes of UK Potsies like Eve and Kathy.
Marcia founded the UKpotsies in February (2011). The first person she approached to join was Tara (Co-founder) as she was one of the only people she had met with P.O.T.S. Tara was instantly enthusiastic and got on board the other lovely ladies Liz, Rebecca and Laura who all do so much to contribute to various POTS projects and the UKpotsies.
Later on Liam found us and joined the team giving a much valued and needed male perspective on living life with P.O.T.S. Olivia also joined the UK Potsies as a great contribution for teenagers and young people suffering with P.O.T.S.
Now we have the most wonderful group of people working in front of cameras and behind the scenes, each person doing a tremendous amount to contribute to this non-profit awareness organisation.
We have each been on our own little journey of ups and downs with P.O.T.S and learned a great deal that we want to share with you, in the hopes that we can stand together as a united community to help patients and families and raise awareness at the same time. Our main aim is to be a friendly, happy group that offers emotional support and reaches out a friendly, helping hand to fellow P.O.T.S sufferers across the UK- and the world.
For more help or information, speak to your doctors and specialists for medical support and advice.Please be aware that any advice provided here should not replace the knowledge or help of your medical professional, and should merely act as a reminder of possible things which may help.
Please see our disclaimer.
