driving with a glove

I’ve been driving this weekend with my compression glove for the 1st time and noticed how slippery the steering wheel is. Has anyone else had this problem? I felt I needed to grip the wheel tighter with that hand which is OK for short journeys but using this hand for extended periods always makes the lympho in my arm flare up.

My gloves are falling to bits. My BC nurse told me I can have new ones every 6 months but I don’t think they will last that long as I wear it all day every day. At 1st I was very precious about it putting on a latex glove if doing anything messy but now don’t bother so they’ve had a bit of a battering. Can GPs prescribe new ones? It feels like being told I can only have 2 pairs of knickers and they have to last 6 months with daily washing!!
Take care.

You could try a driving glove on top of the compression glove. I only wear mine around the house, or for gardening, but I can imagine it would be very slippy.

Just a thought - a golf glove might be better, as you would not have to buy a pair.

Hi littlemrs

Would a (different type of) steering wheel cover be any help, perhaps in addition to the driving glove?

6 months is the maximum life of a compression garment that is worn every day, or every other day; depending on lifestyle some people wear theirs out much faster than others.

Unfortunately, it boils back down to money as usual (hence the rationing of the sleeves by your bcn) and you could try your GP for a prescription, but he might need info’ from your bcn first, so then you might be up the creek without a proverbial.

Do you manage to get to a lymphoedema clinic? (If not, now might be the time to insist on a referral). They might have more flexibilty in what kind of sleeve they can give you, and how often you can have it.

If you can afford it, it is possible to buy off the shelf (as well as custom) ones yourself from many of the major manufacturers (eg, Haddenhams, Medi), although they are likely to need confirmation from your bcn/lymphoedema nurse of your measurements and the compression class you need. That shouldn’t be a problem tho’, because you won’t be costing the PCT any money!!!

Also typing ‘Activa’ into the search engine for these forums will bring up info’ on how to order an Activa sleeve through your chemist.

Also, if you are seeing, or know of, a private lymphoedema therapist (mlduk.org.uk/), they can usually measure and order sleeves for you.

There are solutions to the worn-out sleeve problem, but most of them involve spending your own money, unfortunately. That seems to be the way it is with lymphoedema. Those who can afford private treatment and sleeves when they are actually needed fare much better.

Good luck with it!

X

S

I phoned my BC nurse who also is my lympho therapist. She listened to my pleas and has issued me with new gloves 1 month early. Sadly the ones I’m using can’t be prescribed so she suggests trying out some other makes and then asking my GP. I was horrified when I was told they cost £30-£40!

Re the driving- it seems to have improved so maybe my new gloves have better grip or I was just nervous as I hadn’t been driving for a while. Thanks for the suggestions.

Hi Littlemrs

Glad to hear your problems with driving have eased!

X

S

Hi,
I have kept the packet the glove came in and given that to my GP. It has all the information for prescribing.
Not all products are available on prescription though