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Author Topic: Pictures of our Magnetic Bumper Stickers On Your Car  (Read 12483 times)
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« on: October 15, 2007, 08:21:11 pm »

Here's Kimmy's rear-end, Ahem, excuse me, her car's rear end of the magnetic sticker
Note~ It's above the ribbon one she has you can't see it that well. For those who recieved theirs in the mail already, take a pic and share it. Let's see our October Lupus Awareness around the world on our cars!! I'll take a pic of mine tomorrow & will post then

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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
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Crabbyla279
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« Reply #1 on: October 15, 2007, 08:26:49 pm »

Momma~
I got mine today!  Totally awesome... could have done without my mother complaining though.  "You're really adveritising your disease, huh?"  I said, "is it really so wrong?" and left it at that.

I'll get my bumper sticker on my car tomorrow.  I'll get that picture soon too...
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« Reply #2 on: October 15, 2007, 09:50:49 pm »

Momma~
I got mine today!  Totally awesome... could have done without my mother complaining though.  "You're really adveritising your disease, huh?"  I said, "is it really so wrong?" and left it at that.

I'll get my bumper sticker on my car tomorrow.  I'll get that picture soon too...

((HONEY))))
I am sorry, I wouldn't of sent you one if I had known your Mom would react like that. I am truly sorry.
If she says anything again, just remind her it's Lupus Awareness month and we are all trying to bring awareness to this illness.
(((Sweetheart)) I feel bad.
Love you,
Momma
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
www.LupusMCTD.com Represents:
1) We are patients helping researchers build a future for the lives of others...
2) Where HOPE is a WORK In Progress
3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients
Crabbyla279
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« Reply #3 on: October 15, 2007, 10:40:54 pm »

Momma~
Awww... don't worry about it... I'm well past the point of caring what my mother wants me to do (or not do as the case may be) regarding my illness.  Right about the time I started college in 2003, I decided that it won't hurt me if those around me know what I am going through.  My mother hasn't quite gotten it yet that I actually get more support than negativity regarding my openness about my illness.  Do I go into all the nitty-gritty details?  No.  Do I answer honestly?  Heck yeah!

For instance, back in September there were several Fridays where the center was moving furniture from one classroom to another so that they could have the floors stripped and waxed over the weekend.  When it came time for the pre-school rooms... my site director literally told me that she'd rather I be outside with the kids than lift anything inside- believe me I would have helped that way- due to my wrists/hands not being able to work like others.  It's a fact of my life!  Why avoid it?  That's what I don't get.  Probably never will.  Mom thinks I "hide" behind my illness... but doesn't want me to do anything either that will dispute that I have anything wrong with me- if that makes any sense whatsoever!  Mainly meaning that she doesn't want me to seem "cured" when I go to my rheumy appointments and such.  Enough said, for now.
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sunnipearl
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« Reply #4 on: October 15, 2007, 10:43:04 pm »

 girlwink Looking great! litbflys
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« Reply #5 on: October 16, 2007, 09:28:57 am »

Momma~
Awww... don't worry about it... I'm well past the point of caring what my mother wants me to do (or not do as the case may be) regarding my illness.  Right about the time I started college in 2003, I decided that it won't hurt me if those around me know what I am going through.  My mother hasn't quite gotten it yet that I actually get more support than negativity regarding my openness about my illness.  Do I go into all the nitty-gritty details?  No.  Do I answer honestly?  Heck yeah!

For instance, back in September there were several Fridays where the center was moving furniture from one classroom to another so that they could have the floors stripped and waxed over the weekend.  When it came time for the pre-school rooms... my site director literally told me that she'd rather I be outside with the kids than lift anything inside- believe me I would have helped that way- due to my wrists/hands not being able to work like others.  It's a fact of my life!  Why avoid it?  That's what I don't get.  Probably never will.  Mom thinks I "hide" behind my illness... but doesn't want me to do anything either that will dispute that I have anything wrong with me- if that makes any sense whatsoever!  Mainly meaning that she doesn't want me to seem "cured" when I go to my rheumy appointments and such.  Enough said, for now.
(((HONEY))))  litbflys
I don't get it. I have never talked that way to my kids. I'm glad that you honestly answer her back. Im sure we all have a story in our families about "a certain family member" and Lupus/MCTD and what they feel about it.
I'm so sorry it's your Mom that is the one who makes the remarks. It's heart breaking to me.

I love you,
West Coast Momma~the one who believes in your health and wants to support you.
« Last Edit: October 16, 2007, 09:34:02 am by Admin » Logged


I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
www.LupusMCTD.com Represents:
1) We are patients helping researchers build a future for the lives of others...
2) Where HOPE is a WORK In Progress
3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients
Adminஐﻬ
"Pay It Forward" ஐﻬ
Site Owner
******
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Gender: Female
Posts: 10407


LupusMCTD Founder ஐﻬ


WWW
« Reply #6 on: December 01, 2007, 02:18:35 pm »

Momma~
I got mine today!  Totally awesome... could have done without my mother complaining though.  "You're really adveritising your disease, huh?"  I said, "is it really so wrong?" and left it at that.

I'll get my bumper sticker on my car tomorrow.  I'll get that picture soon too...
Bumping this up in case we all forgot... LOL
Let's take pics of our cars with our stickers on them.
Kimmy, I'll get yours replaced as soon as I get more ink cartridges.   LUAW
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
www.LupusMCTD.com Represents:
1) We are patients helping researchers build a future for the lives of others...
2) Where HOPE is a WORK In Progress
3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients
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