Hello .......... my name is Chris .... and i am new here.......does anyone here have information where i can buy a mucus sucking machine ......thanks in advance in advance ......Chris
Mucus sucking machine: Hello .......... my... - PSP Association
Mucus sucking machine
Hi Chris,
Welcome to this site.
Are you in the U.K? I googled Saliva suction pump, showed the picture to the GP and said it’s what my husband needed. He contacted the district nurse and she acquired one for us. It was a Devilbiss Vacuaide Portable suction machine. It would have cost us nearly £400 but the good old NHS loaned it to us.
Nanna B
Hi Nanna B ........ Thanks very much ......... i will try going down that route ...... tell me did your husband find it helpful ?
Chris
Yes, it was very useful. I know some living with PSP can use it themselves but I had to help my husband. He had so much saliva, dribbling constantly until his last 9 months or so, when the saliva became very thick but the machine still worked.
XxxX
We also used the DeVilbiss suction pump. Worked well but a little nerve-wracking for the caregiver and person with PSP.
If you are in the US, your MD can write an RX for this.
I also got on from NHS not very good at using it, get frightened I am going to push the tube down to far xxxx also George doesn’t really like it xxxx