LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » General Support » hearbreaker: "i'm just gonna lie here and try to figure out what is wrong with me"

 - UBBFriend: Email this page to someone!    
Author Topic: hearbreaker: "i'm just gonna lie here and try to figure out what is wrong with me"
lpkayak
Honored Contributor (10K+ posts)
Member # 5230

Icon 1 posted      Profile for lpkayak     Send New Private Message       Edit/Delete Post   Reply With Quote 
this is what my mom said for 7 years as she lay wasting away with undiagnosed lyme (dx was abnormal onset dementia)

i was just reminded of it as i was ansering another post...the words came out of my mouth, "i'll try to figure it out.."

this has happened a lot . as i get to be her age when confusing symptoms set in to her...i am getting the symptoms and it is like a light bulb going off...ohhh! that's what was wrong with her...she had lyme. i know this happens to others of you.

it was sooooo sad as she lied in the nursing home bed and just said-she didn't want to be a bother...she would figure out what vitamin she should take to feel better...

her boes/cartilage/i don't know...wasted away so much she had to have casts on the outside of her body to hold her arms into the sockets...but she couldn't use her arms or hands for years...couldn't swallow real food or liquid---needed some inbetween concoction...

it was a blessing last may when she let go and went to be with her mom and brother in heaven...

WE NEED TO FIND A CURE FOR THIS HORRIBLE DISEASE!!!

i can't share this with my 5 younger siblings cuz they are all in denial. anyone else want to share about their loved ones?

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm sure that both of my parents had Lyme. It was too late for both. We were all exposed to hundreds of tick bites in the 50's.

My dad ended up with "Parkinson's" by early 1980. He passed away in 1993 after much suffering. He would have been 90 yrs old this June 7th! Hard for me to imagine that!

My mother had all kinds of things wrong with her and she took tons of meds to keep her going. Her heart and kidneys slowly deteriorated. Her mind was a mess after 4 major strokes, but she still knew everybody and knew what was going on. Short term memory loss was the main problem.

She passed away Dec 18, 2005. I miss them both, and only wish we could have figured out this "Lyme thing" earlier.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
lpkayak,

That was one of the saddest things I have read in some time.

Don't know what to say except I am so sorry for your loss.

Lymetoo,

Had read about your father before, but didn't realize you felt your mother also was undiagnosed.
-------------------------------------------------
Somehow we have got to get the word out or a whole generation is going to end up in the same boat -- this whole tickborne illness thing just seems to be exploding exponentially.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by seibertneurolyme:

Lymetoo,

Had read about your father before, but didn't realize you felt your mother also was undiagnosed.

It was my main motivating factor while going through the hell of treatment. I knew what would happen to me if I didn't get rid of this stuff.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Kayak, thank you for sharing your very sad, and true story of your parents with undx lyme disease.

I also feel my late Dad had chronic lyme since the age of 7 or 9. He had a whole lifetime of problems, but overcame majority ofthem ... so stubborn; the Norwegian in him! uffda [Big Grin] Dad was 86, 3 months short of his 87 ... what a life he had in/out of hospitals.

I relive certain comments like this with my lost loved ones. Here's a special hug [group hug] and kiss for you. [kiss]

IP: Logged | Report this post to a Moderator
dontlikeliver
Frequent Contributor (1K+ posts)
Member # 4749

Icon 1 posted      Profile for dontlikeliver     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ipkayak,

Tell me about it. I can sympathize.

My mother's also in a nursing home, paraplegic and incontinent, and mentally somewhere inbetween schizophrenia and dementia. She lies on her 'hospital bed' 24/7 and stares at the ceiling.

When I do get to visit her, about once a year as she's in another country from me, she doesn't really know who I am but when I say my name, she'll say "I had a daughter called that". And, when she has a more lucid moment she'll say "I'm glad you're here, you've got to save me, get me out of this place". But, there is NOTHING I can do. (but leave her there)

I can't believe she is still even alive. I don't think anyone can. I would put money on that she also has Lyme, especially because I know her troubles started when she was 7 and got meningitis, which left her paralyzed for several months in the 1940s. After that, she apparently started to get episodes of hallucinations, but I guess she otherwise appeared more or less normal until 1968......from which point she has descended into living hell.

I cannot even get her tested because she has to give her informed consent to that, but not much chance she is going to do that when she's 'in space'. And, even if she got tested, what do I do with that?

These things are tragic. I'm sticking my head back in the sand now......

DLL

Posts: 2824 | From The Back of Beyond | Registered: Oct 2003  |  IP: Logged | Report this post to a Moderator
char
Frequent Contributor (1K+ posts)
Member # 8315

Icon 1 posted      Profile for char     Send New Private Message       Edit/Delete Post   Reply With Quote 
So many heartbreaking stories. I am so sorry to hear of your parents' pain and the hurt it has caused the whole family.

Lyme treatment is so difficult, but WE have the opportunity to get better. Why us? I don't know but these stories make me realize how GRATEFUL I should be/am that my kids and I can get better.

Thanks for sharing!

Posts: 1230 | From US | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
dharmacleaning
LymeNet Contributor
Member # 2114

Icon 1 posted      Profile for dharmacleaning     Send New Private Message       Edit/Delete Post   Reply With Quote 
As Tutu says. it's a motivation for me to keep trying to get the right treatment. My dad had Lyme several times and wasn't treated correctly. His erratic, paranoid behavior was dealt with by the nursing home with a powerful anti-psychotic which landed him in a wheelchair. He lasted 3 years before the Rispidal(sp?) gave him a stroke, which he died from. Even though his neurologist said it was Lyme, nobody did anything. My mother has never been tested for Lyme, even though she LIVED for being on the beach. She has polymyalgia, and even though we're 30 years apart in age, we act the same - overwhelmed by everyday living, shaky, tired, lying down the moment we can. The usual overall body problems and pain and exhaustion. That's why I keep trying to get better. love dharma
Posts: 731 | From NH | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
dontlikeliver
Frequent Contributor (1K+ posts)
Member # 4749

Icon 1 posted      Profile for dontlikeliver     Send New Private Message       Edit/Delete Post   Reply With Quote 
dharmacleaning,

Can anti-psychotics (which my mother are also on) cause you to end up in wheelchair?

She is in a wheelchair for the last several years, but I can't get anyone to tell me why.

My grandmother, who's 90, thinks (and she's a bit ditzy so I can't trust her) that she fell in the shower during one of her spells in mental hospital and after that could not walk due to bad back pain (also incontinence)...I don't knwo what the truth is, and nobody will/can tell me who is a doctor without my mothers informed consent which she is too sick to give...and my grandmother is still her 'guardian' of sorts making it very difficult for me to get accurate info.

Posts: 2824 | From The Back of Beyond | Registered: Oct 2003  |  IP: Logged | Report this post to a Moderator
dharmacleaning
LymeNet Contributor
Member # 2114

Icon 1 posted      Profile for dharmacleaning     Send New Private Message       Edit/Delete Post   Reply With Quote 
All I know is that one day my father was walking, the next day in a wheelchair. I suspect the meds. But without them, he became frantic, and broke several ribs falling as he tried to get out of the hospital bed ( the sides were up). I also noticed he could no longer write. The meds kept him calm, but I wished and wished that I had known then what I know now and urged drastic Lyme action to see if the neuro damage could be fixed.
Posts: 731 | From NH | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.