National MS Society, Minnesota Chapter

A little unexpected note, email, phone call. Also - I believe a true, heart-felt thank you speaks volumes. This is what I will do - too often in the craziness of our lives, we forget to stop and look our caregiver/partner in the eyes and say:
"... thank you."

i am! excited too...

Nuts! I missed it... oh well. I already know about MS :). I think it would be pretty effective to bring in some balance boards (the ones with the board on top of a half-ball) and have people stand with one foot on each. Then have them do things that involve standing - even something like "washing dishes" or "cooking" - so they can see how much more... Read More work and energy it takes to balance properly. Or have them shave/brush teeth with their non-dominant hand. Or strap on 10 lb ankle weights and have them run...

I always tell people it is like putting the smallest tightest gloves on your hands thats how my hands feel- same with putting a size or 2 smaller shoes on but the electric cord is the easiest to explain.

I feel I not only have a care partner but a care family- my whole family and extended family are a huge support!!! Even my grandsons they keep me going!!!!!

It's not a matter of preference. Ultimately you need to look at what fits the needs of your family. Some partners may choose to hire a caregiver-- if they themselves are incapable of partaking due to other obligations. I give thumbs up for both the Caregiver and Carepartner.

Depends, a cane, a bottle of Mountain Dew, with a sign that reads "I'm doing great, you?"

Changed my mind; a pin cushion.

Yes. Follow me too! Kkkaty

We're following you now, Katy! Thanks for the invite!

I haven't twittered yet!

woohoo at least money going somewhere good :)

I hope this will mean getting a lot closer to having a cure!

I have been going to AAAOM for just the last month, and have been so, so pleased with how I am feeling! I highly recommend this!

There needs to be more things available up here on the Range instead of always in the Cities. I can't get to most of the things offered due to I have 3 kids and a husband and everything is so far away!! Sucks when you would like to participate in so many things but it is impossible when they are always so far away!

Tammy,
You can call the Minnesota Chapter at 612-335-7900 or 800-582-5296 to get more information about insurance options. Our information specialists are very knowledgeable and can help you determine what options you have so you don't have to keep going without insurance! You can also call the Disability Linkage Line at 800-333-2433 for more information about insurance options that you might be eligible for.

I do know that the Chronic Disease Fund can help out in difficult times. They cover whatever my insurance doesn't. It's awesome, but I don't really know who you'd get in touch with. Google it. :D