A woman in my support group has been battling Lyme Disease for 5 years now and her LLMD lost her 2 1/2 years ago. She was doing fine for awhile until 5 months ago. She woke up an could not feel her left leg and by the end of that month she could not find feel the entire lower half of her body and has been paralyzed and in a wheelchair ever since. Since she is in a wheel chair she lacks working and can barely even afford the internet let alone find another LLMD in her area. She is still waiting on SS/Disabilty but has been waiting for a 18 months now. The LLMDS ppl give her seem to have lost their license or are not accepting new patients. Does anyone have a Minnesota LLMD list so I can mail it to her so that she can go down the list and call all of them? please this one is desperate. She is on an O2 mask bc drs are misdiagnosing her with ALS even tho she has 5 blood tests that prove she has lyme and the only reason she had to stop treatment was because her LLMD lost her License. If anyone has an LLMD list for Minnesota could you please send it to me please? She has a neighboring state of Wisconsin also which is only 20 minutes from her. So if you have those state LLMD lists I would appreciate it if I could get those listings. Im on my whitz end. This woman is like a second mother to me and all I want for her is to at least feel better and get some relief. Id rather it be me then her to be honest with you. Please help us!
Posted by aubsdaddy (Member # 21128) on :
sorry I wanted to post this again for people who
cant see double spacing.
A woman in my support group has been battling
Lyme Disease for 5 years now and her LLMD lost
her 2 1/2 years ago. She was doing fine for
awhile until 5 months ago. She woke up an could
not feel her left leg and by the end of that
month she could not find feel the entire lower
half of her body and has been paralyzed and in a
wheelchair ever since. Since she is in a wheel
chair she lacks working and can barely even
afford the internet let alone find another LLMD
in her area. She is still waiting on SS/Disabilty
but has been waiting for a 18 months now. The
LLMDS ppl give her seem to have lost their
license or are not accepting new patients. Does
anyone have a Minnesota LLMD list so I can mail
it to her so that she can go down the list and
call all of them? please this one is desperate.
She is on an O2 mask bc drs are misdiagnosing her
with ALS even tho she has 5 blood tests that
prove she has lyme and the only reason she had to
stop treatment was because her LLMD lost her
License. If anyone has an LLMD list for Minnesota
could you please send it to me please? She has a
neighboring state of Wisconsin also which is only
20 minutes from her. So if you have those state
LLMD lists I would appreciate it if I could get
those listings. Im on my whitz end. This woman is
like a second mother to me and all I want for her
is to at least feel better and get some relief.
Id rather it be me then her to be honest with
you. Please help us!
Posted by LymeXtu (Member # 24590) on :
Just zipper in the state name where you seek a LL doctor. To join for discussion, best to join in your own state. -
Posted by Keebler (Member # 12673) on :
- aubsdaddy
I hope she finds what she needs soon.
About the format, you do not need to double space all your posts when adding white space, for future reference.
It's a lot harder to do double spacing and, for many that can also be hard to track as can solid text. No need to redo above but to save you time in the future, it may be good to know that the 3-4 line max for short paragraphs just seem to work better for tracking of eyes.
That's about 5-6 lines when composing in the smaller box.
Not ignoring any details you posted but My eyes just could not read either post above (the nystagmus shakes all the words). Still, with your headline, I got the main point. I hope the links for MN group and online support help or or her advocates to locate a good LLMD. -
Posted by Lymetoo (Member # 743) on :
Keebler is right. I had trouble reading either one. It's so weird that it's that way for so many of us!!
Aubsdaddy.. I sent you a message!
Posted by LymeXtu (Member # 24590) on :
***Reposting for Aubsdaddy--with spacing****
A woman in my support group has been battling Lyme Disease for 5 years now and her LLMD lost her 2 1/2 years ago.
She was doing fine for awhile until 5 months ago. She woke up an could not feel her left leg and by the end of that month she could not find feel the entire lower half of her body and has been paralyzed and in a wheelchair ever since.
Since she is in a wheel chair she lacks working and can barely even afford the internet let alone find another LLMD in her area.
She is still waiting on SS/Disabilty but has been waiting for a 18 months now.
The LLMDS ppl give her seem to have lost their license or are not accepting new patients. Does anyone have a Minnesota LLMD list so I can mail it to her so that she can go down the list and call all of them?
please this one is desperate. She is on an O2 mask bc drs are misdiagnosing her with ALS even tho she has 5 blood tests that prove she has lyme and the only reason she had to stop treatment was because her LLMD lost her License.
If anyone has an LLMD list for Minnesota could you please send it to me please? She has a neighboring state of Wisconsin also which is only 20 minutes from her. So if you have those state LLMD lists I would appreciate it if I could get those listings.
Im on my whitz end. This woman is like a second mother to me and all I want for her is to at least feel better and get some relief. Id rather it be me then her to be honest with you. Please help us!
Posted by Lymetoo (Member # 743) on :
Ahh.. thanks!
Posted by Rivendell (Member # 19922) on :
sending PM
Posted by hopingandpraying (Member # 9256) on :
PM sent.
Please break up your posts into 2-3 sentence paragraphs, as there are people on Lymenet who cannot read large blocks of text due to neurological problems from Lyme. Thanks.