What's Wrong With You?

#602
#602
BadJerry20 said:
I'm not a fan of dogs, just too needy for my tastes.
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It's the beer goggles. They look good til the next day, then they wanna stay and everything. There's never a nice way to ask them to leave.
 
#603
#603
Weezer said:
Never trust a woman who doesn't like dogs. She has no heart.

Now you need to find out if she has any shame. Ask her if she'd like to do a little horizontal cardio.
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That's a bunch of crap. I've known her since 2006 she's a friendly likable person.
No I'm not going to ask her that.

I've been running on the treadmill for this whole year using non running shoes that's what makes it harder.
But lucky for me I do have a pair of running shoes that I can use.
 
#604
#604
firestorm said:
That's a bunch of crap. I've known her since 2006 she's a friendly likable person.
No I'm not going to ask her that.

I've been running on the treadmill for this whole year using non running shoes that's what makes it harder.
But lucky for me I do have a pair of running shoes that I can use.
Click to expand...

Depends on the shoe color
 
#605
#605
firestorm said:
That's a bunch of crap. I've known her since 2006 she's a friendly likable person.
No I'm not going to ask her that.

I've been running on the treadmill for this whole year using non running shoes that's what makes it harder.
But lucky for me I do have a pair of running shoes that I can use.
Click to expand...

She could be pretending. I wouldn't trust her. Dogs have a sixth sense about this kind of thing.
 
#606
#606
firestorm said:
That's a bunch of crap. I've known her since 2006 she's a friendly likable person.
No I'm not going to ask her that.

I've been running on the treadmill for this whole year using non running shoes that's what makes it harder.
But lucky for me I do have a pair of running shoes that I can use.
Click to expand...

She sounds like a ****
 
#610
#610
firestorm said:
That's a bunch of crap. I've known her since 2006 she's a friendly likable person.
No I'm not going to ask her that.

I've been running on the treadmill for this whole year using non running shoes that's what makes it harder.
But lucky for me I do have a pair of running shoes that I can use.
Click to expand...
Is it just me or do the last two sentences contradict each other? Am I missing something?
 
#616
#616
The Ron Mexico said:
Is it just me or do the last two sentences contradict each other? Am I missing something?
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I haven't ran on the treadmill in a long time so unwisely I was using the wrong kind of shoes.
Not only is this bad it helps to make the running harder. Think of trying to skate on ice with shoes.

I've woken up from dreams I didn't want to wake up from which leaves them with cliffhangers.
I guess I'll buy those lunesta sleeping pills to go to sleep and stay asleep.
 
#618
#618
I have Lyme Disease.
Was diagnosed after 4 years of multiple diagnosis and doctors, I was diagnosed in April 2015.
Did I mention a psychiatrist was one of my doctors because it was "all in my head"?
Turns out it was in my head, a brain infection.

I have a port a Cath in my chest for IV s, 7 antibiotics, prescriptions, supplements, etc.
It is late stage Lyme. Very little hope for a cure. I am left with debilitating fatigue, severe joint damage, brain fog, numbness and burning in my extremities, the left side of my face and lips are numb always, chronic sore throat, swollen lymph nodes, after little exertion I collapse, and more.
Haven't been to a Tennessee game in 3 years.

Hoping to fund a trip to a clinic in Germany having success with Lyme. The treatments are not available here.

Oh did I mention I also have PBC (primary biliary cirrhosis) Walter Peytons disease.

Ok start your violins......Now!!!
 
#620
#620
Red13 said:
I have Lyme Disease.
Was diagnosed after 4 years of multiple diagnosis and doctors, I was diagnosed in April 2015.
Did I mention a psychiatrist was one of my doctors because it was "all in my head"?
Turns out it was in my head, a brain infection.

I have a port a Cath in my chest for IV s, 7 antibiotics, prescriptions, supplements, etc.
It is late stage Lyme. Very little hope for a cure. I am left with debilitating fatigue, severe joint damage, brain fog, numbness and burning in my extremities, the left side of my face and lips are numb always, chronic sore throat, swollen lymph nodes, after little exertion I collapse, and more.
Haven't been to a Tennessee game in 3 years.

Hoping to fund a trip to a clinic in Germany having success with Lyme. The treatments are not available here.

Oh did I mention I also have PBC (primary biliary cirrhosis) Walter Peytons disease.

Ok start your violins......Now!!!
Click to expand...

You forgot to mention you're married to Slice. :)
 
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#622
#622
I don't like psychiatrists, or psychologists for that matter. I've been to several, and they've all seemed more absorbed with themselves then they did about helping me with my BPD. I'm sure there are some good ones out there that actually help people, I just haven't met one.
 
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#623
#623
Red13 said:
I have Lyme Disease.
Was diagnosed after 4 years of multiple diagnosis and doctors, I was diagnosed in April 2015.
Did I mention a psychiatrist was one of my doctors because it was "all in my head"?
Turns out it was in my head, a brain infection.

I have a port a Cath in my chest for IV s, 7 antibiotics, prescriptions, supplements, etc.
It is late stage Lyme. Very little hope for a cure. I am left with debilitating fatigue, severe joint damage, brain fog, numbness and burning in my extremities, the left side of my face and lips are numb always, chronic sore throat, swollen lymph nodes, after little exertion I collapse, and more.
Haven't been to a Tennessee game in 3 years.

Hoping to fund a trip to a clinic in Germany having success with Lyme. The treatments are not available here.

Oh did I mention I also have PBC (primary biliary cirrhosis) Walter Peytons disease.

Ok start your violins......Now!!!
Click to expand...

Do you have to do a regular course on the antibiotics? When I was in the hospital, that's what I hated most. They were running two IV lines, pumping various antibiotics through me because they couldn't determine where exactly the infection was that had me running a fever. After a while, your veins start to burn. Probably sounds weird considering all that was going on with me, but that was what I hated most.

Is the clinic in Germany doing trials, or have they moved on to more of a treatment stage? Have you researched how to actually get into their program? I was just wondering if there were criteria you had to meet? And what exactly goes into the expenses for that kind of trip? I know Slice can be a bit prideful, but maybe we could start a fund in the Pub. Others have done it.

Thoughts and prayers are with you.
 
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