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Stairlift Rental Advice

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    Stairlift Rental Advice

    Well finally decided we need a stairlift as Craig’s grip has gone. Been looking through previous posts and found Acorn that do rentals (don’t want to purchase due to the unpredictability of MND!!) does any of you gurus know of other companies that you would recommend for rentals. Thanks in advance (as always)

    #2
    Hi Lynne,
    I couldn’t find any rental ones when I looked a while ago but I did buy a secondhand one from Higher Elevation. It did save a bit but still pricey I know. Good luck. X

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      #3
      Lynne11013 hi. When I first had a visit from the mnd nurse she said to me that the mnda will arrange for the installation and free rental for the first 6 months and then the patient continues to pay the small charge of rental.

      We didn't go ahead as I don't yet require a stair lift but its good to know the options are there. Xx
      Diagnosed June 2022. Confirmed MND. Limb onset. Symptoms started November 2020.

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        #4
        I wish I'd done that. I've just had ours removed. I paid quite a bit even though it was 2nd hand and only got £75 for it which I asked them to donate to Mnda. I was in a rush to do it because we had suddenly hit a crisis point.
        when i can think of something profound i will update this.

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          #5
          She tried to get me to go ahead in June but as I said I didn't need it yet we would be paying for rental before needed to. Apparently they use reputable local firms to install it etc. And then they remove it when no longer required. U pay the rental after 6 months.
          Diagnosed June 2022. Confirmed MND. Limb onset. Symptoms started November 2020.

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            #6
            I rent a stair lift from Direct Stair lifts.... not sure what areas they cover, but they come quite a long way to install and service mine.

            It was about £1300 installation (curved staircase and complicated at top) then £60 each month for rental. Not a brand new one, clearly refurbished, but does the job and they sort issues quickly.

            I didn't realise MND Association could have helped me rent one. Mine is not perfect and I probably could have got one more suitable (it's fine for most, but my legs are far too short and dangle)
            Diagnosis confirmed as atypical ALS Jan 2022 (age 46) after several years misdiagnosed.

            Symptoms began in left foot 2017. Now widespread. Powerchair user, useless left arm and clumsy right hand but generally positive!

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              #7
              Hi zante, I spoke to MNDA connect this morning as I was told they helped with rental and they advised me that they could help with a grant.
              Last edited by Lynne11013; 31 October 2022, 21:03.

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                #8
                Lynne11013 Lynne, if your stairs is a standard straight type, it's no harm to get a quote or two for a 2nd hand stair lift and see the difference in its cost v renting.

                Also factor in an annual service and if any come with a warranty. xx
                ​Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
                Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.

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                  #9
                  Lynne11013 we got a stair lift via our O T free of charge, ( brand new). Ask your O T first before spending your own money. Some local councils have separate funding for certain disability items.
                  It’s been a god send for my husband. Good luck. Xx

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                    #10
                    Hi piglet, unfortunately we can’t get any assistance from the council as it’s means tested. As my husband is a retired police officer his hard earned pension means we are not eligible.

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                      #11
                      I bought a second hand stair lift via our mobility shop. I have a curved stair case which he was able to build around the curve. Unfortunately I’m no longer able to sit on it now but my mum is now using it.

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                        #12
                        Hi Lynne11013

                        I know there is a campaign running to encourage Local Authorities to use their powers to ensure they meet the needs of people living with MND, including fast tracking applications for support and removing any financial assessment for people applying for Disabled Facilities Grants. Maybe check with your Council to see if they have signed up?

                        Act to Adapt (mndassociation.org)

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