Chronic Lyme Disease

My life with chronic lyme disease and co infections. This is a GREAT day for me,very few and far between. Apparently it also makes me itch worse than I thought. Most people w/ Lyme don't remember getting bit, so get in to an LLMD if you think you have it.

Category:

People & Blogs

Tags:

• Chronic Lyme Disease
• Lyme
• LLMD
• CFS
• Fibromyalgia

[covielloclown]

this is an amazingly brave and important video. it takes guts to put yourself out there in order to help others.

[Straften]

That's exactly what I'm going through! It's a different kind of tired. Even my girlfriend thinks I just need to man up, and she knows me. I'm not and have never been the kind of person who doesn't want to work. Two years ago I was stick fighting for fun. Now I get tired from walking

[AdaLambaKat]

Hi.. Dude i feel ya! Ive been SO sick x3 yrs, but we've traced it back2at least 10 yrs ago! I NEVER knew i got bit!! I hav memory probs, sometimes i cant say certain words, lose my train of thought. Im not workin. Ive NO social life becuz most of the time i am in so much pain that i cannot go out. FEEL FREE 2contact me & we can exchang email or whatever.I have vids that I started summer 2011& was goin2upload-i guess i was embarrassed2do it, but seein u&so many others-Im doin it! Hang in there!

[eveavent]

Wow, you are living my exact life only I don't take all the meds anymore. It just doesn't help. I got sick in June of 1990. I was a vivacious 35yr old woman and now I am 57 and pretty much in the bed all day. You are so right about all the crazy symptoms and the exact reaction of the doctors. They tell me, here in Lubbock, that I can't have Lyme because it's an East Coast diesease!!! Crazy.

[covielloclown]

wishing you all the health and happiness in the world. you are so cared for-always!

[missvitreous]

It's def. not a coincidence that people everywhere have it. Friends of friends, the receptionist at the dentist's office, patients at the dentist's, a few relatives. I hope you beat this. I hope I beat this lol. All lyme patients need proper treatment asap. I hope this stigma around it dies as well.

[DiegoFuckinMarino]

Dude, message me. I really want to share some stuff and talk to you about this cuz there are too many things in this video I can relate to but I don't have enough room on here to post it!

[DiegoFuckinMarino]

I know where your comin from man. I'm on a similar regimine as you, 4 diff. antibiotics and 7 diff supplements. I started back up in January, not to sound like a debbie downer, but Lyme ruined a lot of aspects of my life lol. I feel like shit constantly and everyone else around me feels fine and no one else understands and they just call me a bitch and faggot or a pussy because I have a hard time moving or I get anxious and that mental fog. I've been called retarded so many times it hurts...

[rodarteba12]

I was diagnosed with Lyme in Texas in September of last year. My blood tests came back negative but I had the bulls-eye rash. The symptoms I had were only flu-like the night the rash began to form. I was on antibiotics for 2 weeks(a little less than yours and you still have it). I'm afraid of still having the disease because the testing seems to come back negative during the early stages. Has long-term treatment helped you improve any? Its a shame there is no effective standard in treating Lyme

[nosmartyr]

I feel for you. Thought I was crazy for 4 years before getting the diagnosis. You're not crazy nor are you alone. So, it just wants us to switch genders I guess, cuz I was hormonally male (and I'm a girl)

[nosmartyr]

@MegaMagicman89 hold up-you've heard that salvia is good for lyme??? tell me more