13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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Geneal
Frequent Contributor (5K+ posts)
Member # 10375
posted
Well.....my unusual name is an Indian name.
In Cherokee it means "Little Star".
It should mean "Walks with bb".
Hugs,
Geneal
Posts: 6250 | From Louisiana | Registered: Oct 2006
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aklnwlf
Frequent Contributor (5K+ posts)
Member # 5960
posted
Like my alias.....Lone Wolf. Course am no longer in Alaska but in Alabama.
Maybe I should change it to something like 'Prancing Armadillo'.
-------------------- Do not take this as medical advice. This comment is based on opinion and personal experience only.
Alaska Lone Wolf Posts: 6918 | From Columbus, GA | Registered: Jul 2004
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Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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lymednva
Frequent Contributor (1K+ posts)
Member # 9098
posted
Mine would be the same as my English name. My full blood Indian cousins all have English names, nothing else.
-------------------- Lymednva Posts: 2407 | From over the river and through the woods | Registered: Apr 2006
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posted
I'm part native american too & don't have an indian name, but I like the idea! Maybe snoozes-alot since I slept for 18 hrs. a day for months on end! I like the humor!!!!
Posts: 81 | From Iowa | Registered: May 2007
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13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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charlie
Frequent Contributor (1K+ posts)
Member # 25
posted
....Chief Bactrim Buzzard...
Posts: 2804 | From Texas | Registered: Oct 2000
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-------------------- Strength does not come from physical capacity. It comes from an indomitable will ~ Gandhi Posts: 562 | From Wellsville, PA, USA | Registered: Jan 2004
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Silverwolf
Frequent Contributor (1K+ posts)
Member # 9196
posted
Helloooo there,
I like this idea!!!
How about : 'Trips-a-Lot' or 'Burping Brain' , or maybe 'Sprained Brain' ?! [My dad used to say I had a sprained brain after a concussion when I was a kid].
Almost from birth I was called 'Sunshine and Stormcloud' always wondered if that was of some Amer-Ind derivation, since I am part Native American Indian.
[We were mostly kept in the dark about the Indian aspect of our background for many years.]
Hmm how about 'Makes Many Potty Stops', on another board I visit, I joke w/ friends that I am 'Princess Potties-A-Lot'.
The amount of my restroom visits is notorious among folks I have to travel with.It can be very frustrating,but I try to laugh...,better than crying!!!
I'll have to come back and read some more,thanks for cheering me up!!!
-------------------- 2006,May-August2006 Dx w/ Lyme/Bartonella/White Matter Lesion Disease on Brain. [ Clinical Dx w/ two positives and several IND's on the tests from Igenex ], Prior Dx of CFIDS/CEBV 1992, and FMS '93-'94 Diabetes*2 Dx 10/'08 Posts: 3581 | From SE Idaho | Registered: May 2006
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posted
Hey....Mighty Herx Alot, your mailbox is full..I like your name, it sounds like some kind of Lyme Super-Hero or legend! Herx-ul-ease
Me Chief Walking Pharmacy
Chokes on Pills
(no disrespect intended to any native americans out there, just having fun....for a change)
My wife found this pretty funny, we have been trying to decide on a new email address (for over a week now) due to excessive junk mail.
After hearing some of these she sugested the new email to be swisscheese (refering to my brain of course)
Im tempted to retaliate with alwayslate or pokeypokey
BJK
-------------------- BJK
Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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Clarissa
Frequent Contributor (1K+ posts)
Member # 4715
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
I actually have a tshirt that says this, so me:
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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Ann-OH
Frequent Contributor (5K+ posts)
Member # 2020
posted
Are we talking about Native Americans here? Had I been born in India, I hope I would have been named Rani which I believe means princess.
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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posted
Hey! Walks into Walls was MINE!!!! I honestly hit my face on the door facing a week ago, and had a bruise in the middle of my forehead and a scrape on my nose! [thought I had broken my nose!]
I was so afraid someone was going to ask what happened to me!!!
How about Snow on Screen?? [get it??]
My brain is fried right now....kinda blank!
Blank Brain??
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96239 | From Texas | Registered: Feb 2001
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at least thats what I almost was a few times recently before my doc removed my driving priveleges.
I just didnt see the.....Moving Van (such a small object to miss)! After I had accidentally driven into a one way lane....going the wrong way! Don't figure
Just came in from outside...now Im
"Stepped in Pom poo"
BJK
-------------------- BJK
Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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Michelle M
Frequent Contributor (1K+ posts)
Member # 7200
posted
"Runs with Glass."
Michelle
Posts: 3193 | From Northern California | Registered: Apr 2005
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
LOL!!! Sorry Lymetoo!! I will now change mine to:
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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posted
I thought of two, pressed the button to post, and now can't remember what they were.
Ummm.....
-------------------- If you don't know where you are going, any road will take you there. - Lewis Carroll Posts: 356 | From Body-PA, Mind-elsewhere | Registered: Dec 2007
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-------------------- If you don't know where you are going, any road will take you there. - Lewis Carroll Posts: 356 | From Body-PA, Mind-elsewhere | Registered: Dec 2007
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Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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Maybe next year....Ill put my 13yr only boy to work!
BJK
-------------------- BJK
Nothing I write here is medical advice...I'm just another lymie sharing how this disease has affected me personally Posts: 175 | From Central Maine | Registered: Sep 2007
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kam
Honored Contributor (10K+ posts)
Member # 3410
posted
This thread caught my eye but have yet to come up with a name...
Maybe it will help some of us who are having trouble coming up with a name
Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002
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Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
My family calls me "Name Meister" I have problems remembering people's names correctly - but I come incredibly close to accurate. Posts: 641 | From So. CA | Registered: May 2008
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