In search of Lympedema pump
Comments
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While even I am lymphedema patient for 1 year now
I do not have information about pump. My lymphedema therapist believes that manual drainage and wrapping are the most effective ways to keep it under control.
Sorry, I cannot help.
Good luck,
new Flower0 -
Thank you everyone for your
Thank you everyone for your responses. I have been taught to do the message therapy at home by my therapist but unfortunately I have a lot of fluid and need a pump to try to remove it faster for relief. I have 3 compression sleeves and 3 hand compression gloves.0 -
Thank you everyone for your
Thank you everyone for your responses. I have been taught to do the message therapy at home by my therapist but unfortunately I have a lot of fluid and need a pump to try to remove it faster for relief. I have 3 compression sleeves and 3 hand compression gloves.0 -
Thank you everyone for your
Thank you everyone for your responses. I have been taught to do the message therapy at home by my therapist but unfortunately I have a lot of fluid and need a pump to try to remove it faster for relief. I have 3 compression sleeves and 3 hand compression gloves.0 -
PumpYvette39 said:Thank you everyone for your
Thank you everyone for your responses. I have been taught to do the message therapy at home by my therapist but unfortunately I have a lot of fluid and need a pump to try to remove it faster for relief. I have 3 compression sleeves and 3 hand compression gloves.
Did you try freecycle in your area? You also might try E-bay. Just a few suggestions. Good luck.0 -
EBay?calvertcrafts said:Pump
Did you try freecycle in your area? You also might try E-bay. Just a few suggestions. Good luck.
I also have lymphedema but it is controlled with the sleeve and gauntlet and manual drainage massage. Have you tried googling?. When I was looking for surgical supply companies online that sold the sleeves, I went to the manufacturers of the sleeves websites and googled the item leading to a list of places that supply them both online and locally. Have you contacted the National Lymphedema Association? Perhaps they could be helpful in finding the pump for you.
Hugs,K0
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