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MissNikkiAnn"When you have an illness with the name "Non-Familial Dysautonomia" (a name that most people, and even doctors, have never heard of), you need a network
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MDJunction led me to that network of people during a very confusing and sickly time. For this I am thankful. And for this reason I try my best to give back to other members the same care and help that I received through MDJunction.
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Parkinson's ForumsLounge - Off topic discussionsif you have lemons make lemonade
03/05/2012 05:04 AM
jaguar62
jaguar62
 
Posts: 285
Group Leader

y'know after missing so much time at my real (paying) job for a few months and just doing little odds and ends around our house . Me and Gena have nearly painted the whole interior but due to the circumstances sometime it was only a wall a day or no work today. but I was thinking if I couldnt perform my real job anymore.. Maybe the Sherwin Williams people would give me a job as a "paint shaker",, (LOL)

Sorry (please dont take it personal) I am pretty bored lately

Love and Prayers

James

Love and Prayers to All
James
Group Leader of Parkinson's Disease Support Forum

My advice is purely personal. I am not a Doctor and there is NO substitute for getting proper medical diagnosis and advice.” Just one caring persons opinion.
Reply

03/05/2012 05:21 AM  Top
Bettyg
 
Posts: 26537
VIP Member
I'm an Advocate

JAMES,

good for you and gina; i loved the note you just sent me.

welcome gina to the board. glad you had a good time lately outdoors enjoying the crafts, sights, etc.

DON'T RUSH BACK TO WORK!

i don't know if i told you or not, but if you ARE CONSIDERING FILING FOR SSDI, ss disability insurance work benefits, IF YOU GO BACK NOW FOR 30-60 MINUTES; your time starts all over for 5 months to wait before you file paperwork to try to get disability work benefits!!

if you are interested, in my signature line is my welcome letter for our lyme board, go down to the area where i mention myself, conniemc, and minoucat for our COMBINED WISDOM on getting approved since we each learned the hard painful way.

HEADED TO BED; long night here.

you could come and paint a few rooms for me in iowa Wink you're broke in just right. lol

hugs/prayers,

bettyg, pd wife

lyme disease group leader

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.

03/06/2012 07:55 PM  Top
Priyeni
Priyeni
 
Posts: 625
Member

If u have time pls tell me who Sherwin williams is....I'm from the other side of the world & dont get some of yr jokes , soreeeeeSmile Wink dont wann miss any fun.
Priyeni

I'm not a doctor so I can't comment on yr meds /physical pain & symptoms but I'm a good listener & will be always there if you need to unburden /vent.

03/06/2012 08:53 PM  Top
lefty4
lefty4
 
Posts: 47
Member

It's a paint making company... but before you purchase paint - they put it in a shaking machine to stir it all up. It's hilarious lol

06/17/2012 06:38 PM  Top
Priyeni
Priyeni
 
Posts: 625
Member

Hey James, u told us this - cld we have some lemonade pls? havent had any made by u, preferably in a Sherwin William's shaker Smile Smile

How's that from someone who hadnt even heard of S.W. Miss yr repartee here. hurry up with yr lemonade mate, yr taking rather long to pick the lemons Smile Smile

Priyeni

I'm not a doctor so I can't comment on yr meds /physical pain & symptoms but I'm a good listener & will be always there if you need to unburden /vent.

06/20/2012 04:18 PM  Top
jaguar62
jaguar62
 
Posts: 285
Group Leader

I switched out the Lemonade for a big tall glass of Crystal Light Lemon flavored Ice Tea. The lemonade was keeping my glands swollen and my cheeks were all puffy and people shied away from me thinking i had something, (imagine that.. the nerve of some people!) any ways it caused a damper in my daily smooching with Genagirl so it had to go .....

So now if Life gives me Lemons I put em in my Iced TEA...

your friend

James

Love and Prayers to All
James
Group Leader of Parkinson's Disease Support Forum

My advice is purely personal. I am not a Doctor and there is NO substitute for getting proper medical diagnosis and advice.” Just one caring persons opinion.

Previous discussions I participated in:
Update
Personal Health Targets
hardship

06/20/2012 05:40 PM  Top
mem2121

Jaguar, you've been quiet for awhile. It's nice to see you posting again!

Watch out for other musicians. We'd had a couple more join since you've been offline.

Smile

Steve


06/20/2012 05:54 PM  Top
oregonnative
oregonnative
 
Posts: 5127
VIP Member

Haha! James, love that about the lemon in your tea now. Can't have puffy cheeks cramping your style! You do mean face cheeks, right? Laughing
Shoot for the moon...if you miss it, reach out and grab a star.
Karen

I am not a medical professional. All comments are based on my own experience and/or from articles I have read.

Previous discussions I participated in:
my luck
Terrific Tuesday!
Where's Cal?

06/20/2012 11:39 PM  Top
Bettyg
 
Posts: 26537
VIP Member
I'm an Advocate

and we lyme disease folks make LYMEAID Wink

good to see you all.

hugs/prayers for you all.

i'm pooped out from 2 full day of parkinson's conferences!

live in des moines, iowa friday

sat. was the LOS ANGELES webcast. I HOPE YOU FOLKS WATCHED!

last yrs. des moines live webcast cost $20-25,000 to put on for ONE day! uffda.

bettyg, pd wife/lyme activist

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.

06/21/2012 03:34 AM  Top
Priyeni
Priyeni
 
Posts: 625
Member

James, Yr back! Love it - lemons in yr iced tea sir! Look forward to more like that one Smile Really good to have u back.

Betty, one Lymeaid coming up ma'am Smile

In the midst of serious discussions, disappointments, anxieties, fears, isnt it nice that we can say silly things that make us smile - so nice for me, Smile

Priyeni

I'm not a doctor so I can't comment on yr meds /physical pain & symptoms but I'm a good listener & will be always there if you need to unburden /vent.
Reply

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