1893 pts · January 30, 2017
Chronic illness humor, silliness and such. No hate
I love u 3000
I did the exact same thing. Have the ID but no driving. BTW taking Lamictal
I have epilepsy for over 35 years. Many face plants later, have a wonderful husband and kids.
We just lost our pug who was 13 years old. The absolute best Breed ever. t
The flashing lights could cause epileptic photosensitive seizures. Only 3% of epilepsy patients have these seizures
I have epilepsy too and have lost 3 jobs. My Dr finally said that working was causing me too much stress and therefore seizures. Epilepsy blows
There is a town in IL that has is called Sandwich as well
I have epilepsy and have had numerous concussions (as do several epileptics). The worst one put a dent in my brain. It showed up on the MRI. Mind blown! I went to Concussion PT. Didn’t know that this was a thing!
Agree!
Growin up as a kid, we used cow tanks as pools. Only now thinkin probably not healthy. p
Thus tis true
Agreed! Always say if there was a bear, I would be his lunch! 🤣
Love this!
Yep!
Thanks for your comment. Really
I am thinking of getting a nerve stimulator. Working thru a ton to get there.
I am a 48 yr old that has had 30 years of pain from my illnesses. Sending healing vibes to you
Thanks! We have new things coming out daily. Hugs
A vagus nerve stimulator would help my epilepsy. Don’t qualify for that. There is also Deep Brain Stimulation. This is a last course e
The thing that helps me the most is gummies. Every night to sleep. Going to a new Doctor in a few weeks.Definitely will keep all posted
Gummies every night is the only way I get any sleep.
Both havent worked so far. I am hopeful
I have a pain condition called trigeminal neuralgia. This is extreme facial pain -also known as the suicide disease.For my pain so far, I have had 4 brain surgeries, countless nerve blocks, Botox, acupuncture, and currently a Tens machine. I also take nerve suppressants and natural weed gummies to help me sleep.DM if you would like to talk more. Many gentle hugs to you.
I have had MS for 23 years-RRMS This disease is different for everyone. Optical neuritis happens to a lot of MSers. For many it is their first symptom. I believe my success can be attributed to good medication, physical therapy and counseling. Happy to talk at anytime
Agreed. RIP
☺️☺️
Righteous!
Nope. Definitely not
Shhh-don’t tell 😂
Love it
I love u 3000
I did the exact same thing. Have the ID but no driving. BTW taking Lamictal
I have epilepsy for over 35 years. Many face plants later, have a wonderful husband and kids.
We just lost our pug who was 13 years old. The absolute best Breed ever. t
The flashing lights could cause epileptic photosensitive seizures. Only 3% of epilepsy patients have these seizures
I have epilepsy too and have lost 3 jobs. My Dr finally said that working was causing me too much stress and therefore seizures. Epilepsy blows
There is a town in IL that has is called Sandwich as well
I have epilepsy and have had numerous concussions (as do several epileptics). The worst one put a dent in my brain. It showed up on the MRI. Mind blown! I went to Concussion PT. Didn’t know that this was a thing!
Agree!
Growin up as a kid, we used cow tanks as pools. Only now thinkin probably not healthy. p
Thus tis true
Agreed! Always say if there was a bear, I would be his lunch! 🤣
Love this!
Yep!
Thanks for your comment. Really
I am thinking of getting a nerve stimulator. Working thru a ton to get there.
I am a 48 yr old that has had 30 years of pain from my illnesses. Sending healing vibes to you
Thanks! We have new things coming out daily. Hugs
A vagus nerve stimulator would help my epilepsy. Don’t qualify for that. There is also Deep Brain Stimulation. This is a last course e
The thing that helps me the most is gummies. Every night to sleep. Going to a new Doctor in a few weeks.
Definitely will keep all posted
Gummies every night is the only way I get any sleep.
Both havent worked so far. I am hopeful
I have a pain condition called trigeminal neuralgia. This is extreme facial pain -also known as the suicide disease.
For my pain so far, I have had 4 brain surgeries, countless nerve blocks, Botox, acupuncture, and currently a Tens machine. I also take nerve suppressants and natural weed gummies to help me sleep.
DM if you would like to talk more. Many gentle hugs to you.
I have had MS for 23 years-RRMS This disease is different for everyone. Optical neuritis happens to a lot of MSers. For many it is their first symptom. I believe my success can be attributed to good medication, physical therapy and counseling. Happy to talk at anytime
Agreed. RIP
☺️☺️
Righteous!
Nope. Definitely not
Shhh-don’t tell 😂
Love it