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Lyme Disease Forums › General & Support › do a fundraiser to pay for treatment

07/23/2011 07:23 PM

do a fundraiser to pay for treatment

jomomma

Posts: 372
Member

I just wanted to pass on a thought to you all. I use to sell tupperware and when you do a fundraiser you get 40% of what you sell.

If you find a consultant who is willing sometimes they will also donate part of their commission.

I homeschool my oldest & when we didn't have much money I would do a fundraiser to pay for my homeschool materials.

As long as you disclose what the fundraiser is for anyone can do it. You don't need to sell the whole , I have Lyme if you don't wish to, unless someone asks what it is for.

SiCk & TiReD oF bEiNg SiCk & TiReD!!!!!!!!!! ;)

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07/25/2011 02:26 AM Top

Bettyg

Posts: 26564
VIP Member
I'm an Advocate

hi jo,

may i ask that you EDIT & |"CUT'| your comments to paste on my topic here on FINANCIAL BURDENS/resources.

would fit this great, and all ideas could be in 1 link ok my new friend hugs

Suggestions for When You Need Treatment and Funds Are Low plus Financial Burdens post towards bottom;

extremely detailed by Melanie Reber

http://tinyurl.com/4es7942

i'm locking this post; will delete it after you add your info to an existing ongoing post.

if anyone else has ideas like this, please add them there. BIG THANKS everyone for continuing to add to my postthere.

bettyg, iowa lyme activist/lyme leader/llmd coordinator

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

Previous discussions I participated in:
Does this sound like Lyme or co-infection to you
Llmd in MA
Long-term effects

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