Betty's Battle with Lyme: 5 years of HELL.
- From: "CaliforniaLyme" <CaliforniaLyme@xxxxxx>
- Date: 27 Nov 2006 08:08:01 -0800
Betty's Battle with Lyme
In July of 2004, I was correctly diagnosed with chronic Lyme disease
after being misdiagnosed for 34 years by between 40 and 50 doctors. I
was also diagnosed with sleep apnea, diabetes 2 and restless leg
syndrome. I was tested with the Western Blot, which needs to be using
all 16 protein bands...all strains of Lyme Disease!
Iowa does not have Lyme literate physicians, so over 1500 Iowans have
gone out-of-state seeking treatment. Most go to Kansas City or
Springfield, MO. At the end of this month, I'm going to Minnesota for
treatment but NOT the Mayo Clinic! Going out-of-state means "going out
of network" so I must PRIVATELY PAY for LLMD treatments, blood labs,
x-rays and out of pocket costs for gas, lodging, food, etc. My first
LLMD visit will cost $600; follow-up with be $400 plus huge lab costs.
"You look perfectly healthy...not sick" said one of my family members.
Oh, what they don't know and can NOT feel the pain and fatigue inside
me! If I were in a wheelchair, used a walker or cane, at least I would
have a visible disability. "It's all in her head." If only those of you
NOT battling Lyme disease knew how much pain and anger you've caused
with your thoughtless comments on our invisible illnesses! We don't
want your sympathy...we only want your support, compassion and someone
to talk to when our flare-up's are bad.
My pain never goes away! I use a heating pad or cold pack on my neck,
shoulders, lower back, thighs, and knees to try to numb the pain.
Do you have any idea what it's like to go to bed night after night,
year after year, and get up just as TIRED as when you went to bed? We
can't reach the level of sleep that heals and rejuvenates our systems.
I soundproof my bedroom to eliminate noise from our neighbor's
driveways, the slamming of car doors, racing engines, dogs barking,
etc.
I was clinically diagnosed with major depression and anxiety and put on
antidepressants - causing me to gain 25 pounds, which caused the
onslaught of my diabetes 2 sooner. I have difficulty concentrating and
performing simple mental tasks. I now point at things 60% of the time
because I can't think of the words.
In July, 2005 I was finally approved on my second SSDI claim after 5
years of HELL.
Betty Gordon
Ames, Iowa
.
- Prev by Date: In the Shadow of Lyme: The Hubbard Family
- Next by Date: Re: How about those Bears....
- Previous by thread: In the Shadow of Lyme: The Hubbard Family
- Next by thread: Galesville Officer Battles Back From Lyme Disease: he suffered such delirium that he didn't know who he was.
- Index(es):
Relevant Pages
|