I find men's shoes are wider and I can wear UK size 7 instead of UK size 8 in women's (if I didn't have lymphoedema I would wear UK size 6). I have a great pair of mens white leather casual lace ups which I will be wearing today, with a dress, to go off on a course.
Not ideal I know but it works for me. I also walk a lot - average 6 miles a day, often more. I wear walking shoes bought from an outdoor shop most of the time, in a size larger than I would previously have worn. V comfortable. Also Doc Martens, likewise in a larger size (I’m wearing UK size 7 when previously I would have worn 51/2 or 6). Now I’ve shifted into Teva open sandals including for walking - though they don’t give the support that the shoes do, they’re much cooler for this weather.Sorry for your problems, I hope you find a good solution for you. Xx
Hi I have the same problem so know how you feel. I went to my GP and explained the situation and was referred to the shoe makers, orthotics I think its called. who visit the hospital.I get my footware made, 2 pairs every 2 years on the NHS. In actual fact I've just had boots made. You get a choice. Shoes or boots.
Not especially stylish, but at least I can get them on every day, and comfortable.
It's worth a try. I'm in Hertfordshire, so if we do this, other counties probably do the same.
'Cozy Feet' have such an old-fashioned name but the shoes are brilliant. My favourite is the all-wool slippers but I have had trainers from them too. Not cheap but certainly suitable for lymphy feet.
I have found my solution. They are Kerrapeds. May be used by nurses applying strapping to infected legs. After years of just being given compression stockings, I had a couple of weeks with firm strapping on both legs. Normal shoes cannot be worn with the strapping so the nurses gave me a pair of these. Bliss at last shoes that fit and do not hurt. Not waterproof and the wind blows through the fabric.
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