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Paula Mieczkowski and
John Connor are now friends 6 months, 3 weeks ago -
Paula Mieczkowski replied to the topic MS Research Australia has Just Released a Lifestyle Guide in the forum Living With MS 9 months ago
Go Australia! When you’re on Medicare in the USA you get sub par aids from Medicare. Sent me a electric wheelchair. Batter died before it was ever outside. They billed the government 31,00$ yes 31,000.00$. New battery? 1,000.00$. Sure, let me write you a check. Other thing to be aware of is that it goes up n down to heights enough to reach…[Read more]
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Paula Mieczkowski replied to the topic A wheelchair accessible van in the forum Durable Medical Equipment 9 months ago
Good luck paying for that. Maybe with your wife working you can afford it. Wishing you luck from West by God Virginia
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Paula Mieczkowski replied to the topic Sexual Dysfunction Common in Men with MS, Review Finds in the forum Living With MS 1 year, 5 months ago
What about women?
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Paula Mieczkowski posted an update 1 year, 5 months ago
What about women???
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Paula Mieczkowski posted an update 1 year, 6 months ago
Certainly feel for you. Frustration is the worst of any infection. When I feel the awful signs of an UTI the bladder spasticity start with a vengeance. If I could double up in pain I surely would. Myrbetriq (sp) helps tremendously and immediately. Antibiotics help too, however they also come with side effects. Side effects aren’t worth i…[Read more]
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Hi Paula,
Big up on the beer!
I live in the magic land of the UK & the NHS so never, ever, have to worry about number of catheters! Indeed the more u pee the better it is for your bladder! Know catheterization is obvious introduction of foreign bodies but anti bac gel helps a lol. Indeed everything that attacks me turns out to be in there…
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Paula Mieczkowski became a registered member 1 year, 6 months ago
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Hi Paula,
Welcome – loads of info, research & experiences on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at the top of each Forum.
Cheers John -
Hi Paula,Thanks for joining us. I’m an MSer from much further back…was DXed in 1980. It was a far different MS world then. (My neuro, BTW, is in Tysons Corner. I’m in MD.)
Ed
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