my lyme story, part 2

i ran out of batteries, so this is the end of my lyme video. :)

Category:

People & Blogs

Tags:

• health
• lyme
• disease
• awareness
• story

[JadyDavisTV]

I have horrible insomnia too! I've been up all night long too. :/ JD

[heiwalove]

it's awful, isn't it?  i've tried everything and nothing works!

[JadyDavisTV]

you're really pretty, keep fighting, it's cool we like to do some of the same things. Great vids.

:)

JD

[heiwalove]

thanks for your sweet comments JD. i was a little delirious when making these videos, but i'm glad you liked them anyway. :) also, your strength is amazing to me -- i can't believe you're only 16!

[ADDIElilqueenie]

Dr. Zhang is the answer.. I am almost normal after being paralyzed, and having lyme everywhere.. If anyone is interested pm me.. I don't work for him ... he has a "cure" for lyme and hep c.. with TCM...

I would have died if I had not found him.

Good luck to you.. get his herbs..

[FloridaSalon]

I would really appreciate any info on your treatment. I am currently taking doxycycline. It keeps me functioning..........but that's about all.

God Bless you ...........

Thanks, Shanda

[valentinosgirl]

You know, I never realized that the flipped schedule was a Lyme symptom! I have lyme and my family just thinks I am crazy to stay up late and sleep late. I thought that maybe it was something that I could help but I'm seeing that I'm not the only one. Sorry, this might sound a little funny, my cognitive function is nil.

[iowabettyg]

heather,

thank you for sharing your story thru both of your videos posted here!

thanks for mentioning for folks to watch or buy the UNDER OUR SKIN lyme documentary by andy abrahamson wilson, and is being DISCOUNTED UNTIL 9-15; so save money & order today! it's outstanding 104 minutes!

my heart goes out to you for family putting you in psych ward. hugs/kisses heather

YOU ARE A STRONG PERSON and will continue telling your lyme story forever.

wishing you REMISSION in near future.

[amishsunshine]

I think it is so important that we all try to be as open about our Lyme sturggles as you have. I am fighting chronic lyme that my general physician diagnosed as "emotional female syndrome". I hope you get better, I hope we all get better... and I have faith that someday people will know what we've all endured and view it with disgust for how our own countries and systems have failed their very people.

[girams]

Thank you, Heather. I have been sick since 1995, had antibiotics in 2000 but still have pretty bad symptoms. I hope you keep video blogging. I do alternative treatment and have found that being on a wheat-free yeast free diet has helped. Maybe your caregivers have some ideas for your diet.

[artsyfart66]

Insomnia..i know that one too...it was 3:30am this morning for me. I can handle pain but the worst part of the disease for me has been the cognitive impairment & depression and the isolation i feel from having others think i am nuts. Also, losing my independence and my job of 12 years due to this illness has been really hard to deal with for me. I wish you much love & healing on your journey! P.S. I have copies of "under our skin" that i give to as many people as i can.

[raemeier]

I hope you're doing well. My partner has lyme and I'm wondering if you'd be willing to share what your specific treatment plan was/is. All the best.

[chiefer99]

Your strength is simply amazing, to go through all that without much help from your family would have been ridicuously difficult. Keep your will power and determination and better days will be ahead.

[thane17]

I just watched your videos again because i love them. I see you haven't posted one in a while and i hope that is because you are having soo much fun living your life and I hope that if you are still sick that you remind yourself of the good days and know that you will get better soon.