#revitalize2016

[@creativesolutionsart-h3o]

I was diagnosed a week ago, after Decades of misdiagnoses. I've probably had this they estimate since I was 7. Brain fog and confusion are my more recent symptoms over the last 10 years, but prior to that I had the opposite my brain was in constant Overdrive. When I see people now who don't act right, I have a whole different perspective. We need videos like this for awareness. Thank you Brave woman.

[@honeybeebusywhatsallthebuz1922]

May god heal all Lyme disease sufferers I hope to help with change and healing everyone

[@AB-bt9eb]

Thank you for speaking out about Chronic Lyme. It's a terrifying and painful disease. Youve done so much to help and I'm so gratrful.

[@Ego-de4dt]

She speaks so well. So down to earth. So classy. So clearly.

[@annlanders978]

She seems like a truly wonderful. person who didn't ever deserve any of this .

[@cristina5507]

Ally thank you for sharing your experience may god bless you in trying to help others 🙏❤️

[@carasun2499]

It's so good to listen to somebody talking that honest. We need more of these warriors!

[@jessicama5799]

I wonder how many case of schizophrenia are some type of illness that causes brain inflammation or Lyme disease.

[@ps-zt7tw]

Thank you, Ally. I read your book around 2016 and was so appreciative that you were honest about your experience. We all need to try to stay in touch with the injustice going on around us because of "profit before health" etc, etc. We all need to hang on tight to ourselves while we take care of ourselves and live according to "do unto others". I know many who can't get adequate treatment for Lyme and many who don't have a clue of the 40 years of not "fast-tracking Lyme" as was done with HIV. Best to you always.

[@graceamazing5981]

Thank you for revealing the 'puzzle' that Lyme causes ! Mine is early (i think/hope) and mild but i have friends who are very seriously affected, and hopefully they will be encouraged when they watch this ! Your message is genuine, understandable, vital and may just be a turning point for some who are distressed with their condition ! We pray you stay the warrior you have become and that you stay healthy ! May God continue to bless you!

[@jackiewatson5665]

I would like to know the details of the homeopathic treatments, the exact meditations/visualisations and diet you feel helped. Your story is inspiring.

[@antohong]

Homeopathic forget it ,that is something you have to believe in it doesn't have any proven medical data.

[@lelamoore7178]

18 years lymes.....i am the storm stay strong ally.

[@dontothepiano]

This was really inspiring. The fact that you were able to talk this freely and fluently about your disease gave me strength in moments where i'm incapable of stringing the most basic sentences together. Hope I'll be able to continue the life I had before all hell broke lose, just like you did. Thank you

[@lefteyeentertainment4693]

Wife has been chronically ill for over 5 years because of Lyme & co-infections. We've spent countless amounts of money trying to beat this, still not better, it is shameful how the government is handling this, especially healthcare. It worries me that even the ultra wealthy cannot buy there way out of this disease. The antibiotics have destroyed gut health, SIBO infections, insomnia, the list goes on. We left the country last year for stem-cell therapy, no real gains made as of yet, waiting for a cure.

[@tarenpenington2548]

How is she doing now?

[@indiabharat5014]

Brain retraining and breathwork will help her. I was like you once

[@roslynodonoghue3810]

Well done for explaining the disease, however for someone like me who has no money, to access homeopath, vitamins and other alternative medicine is hard, untreated chronic lymes can lead to dementia type parkinsins. Been bed ridden now for 3 years and my cognitive function is getting slowly worse. Hard to accept and scary to think about.

[@sararao8429]

So sorry hope u r better now, I'm not bedridden, cognitive decline

[@JP-xs5lo]

A little late to say the least but there should be emergency authorization for drugs to treat persistent tick borne disease immediately. We can fight this and hold the cdc accountable!!!!

[@JP-xs5lo]

This same thing happened to me I had tick bite diagnosed from Stoney brook university tick borne disease research center after 2 years of misdiagnosed from va medical system and I was gas lighted by my family into mental ward at public hospital were they would not recognize my diagnoses or tick borne disease all together and I was on picc line 2 years and had best llmd right around the corner and my family turned there back on me they pulled the cdc side against me.

[@WilliamSchober-l8g]

That’s perfect…! Thanks for sharing your experience. Although now much more light is show on that specific illness. The word chronic is scary enough. Thank you for the information again.😊❤

[@shannoncrozier3391]

glad you had that. I've been buses by family child loss a d everyone abandons you cause they are not only sefish but do not get many things and if you are not rich. then le treatment is a struggle. on top of. the other crap we or I have gone through 7 years of hell ND I think most people are ignorant to Lyme. dpdr. and depression. thanks for sharing

[@Jamal287]

I really cried so hard watching this.......

[@Ego-de4dt]

Enigma Co cried so hard??? Why?

[@jenka_world6956]

I did too

[@charlotteriley7318]

Lyme is torture. Terrible crimes against humanity.

[@mycocoadreamz]

Thank you Ally & well done. It is such a harrowing & never ending journey. Your talk was beneficial to hear & uplifting. All my love & best wishes to you 🙏💚💚💚

[@derekeccles7612]

I got diagnosed with 13 different Tick born infections through armin labs in Germany they test for multiple infections,my test was called tick plus,13 infections 9 down 4 to go it has been a rough year I am down 93lbs since March

[@KyzerGB]

Just sent my bloods to armin labs also. I'll be going stem cell therapy for lyme if it's comes back. As Drs here won't accept results from overseas . 🙄

[@derekeccles7612]

@@KyzerGB does the GB in your name stand for great Britain,if it does there is a doctor up the north if England that does, I'm in Ireland and have seen a Lyme specialist here

[@KyzerGB]

@@derekeccles7612 Yes I'm from the UK. Thank you for replying. Have you had much luck with the dr ?

[@derekeccles7612]

@@KyzerGB if you check up for a Lyme literate medical doctor (llmd) you should be able to find there name,yea 5 antibiotics a day and a few supplements every day it totals about 15 in all every day and i have gone from not being able to walk or get out of bed to being up walking around I'm feeling a good bit better already and that's only after 3 and a half weeks,its going to take 6 months to a yeat to fully recover buy I'm well on the way after such a short time,just to let you know it IS treatable and you can make a full recovery contrary to what you hear and read online it just takes time and the right medication Lyme us bacteria they just need to find every strain

[@KyzerGB]

@@derekeccles7612 Have you read the story of them who healed in 60 days ? Will Wiegman his name is. Also look into b17 kernels. I'm able to walk and work as I have to . Have to support my family and daughter who's only 3. Just my one leg calf hurts like hell some days and have numb arms now and then. All this from a bad uti and being put on lots of antibiotics for it. After this came along to ruin my life. Some days I have the hangman loose feeling . 🙄😫

[@gavinosolis6493]

Amazing speaking thank you for sharing

[@talias7585]

6+ strains + bartonella & babesia y’all

[@Steve.191]

Thank you 👍

[@Ego-de4dt]

The same father who said “no stone should go Unturned” is the same father who threw his hands up and had your drugged and TRICKED and admitted to a psyche ward. So gross.

[@sariahsky8128]

I agree i would freak out, god was over her , she did get diagosed . It is scarey that a lot are at psych, does ot effect me like that, my gr. fried from 7th grade , it does a lot. sorry 2 keys just stopped workig hmmm

[@betrion7]

Which resulted in getting her diagnosis. Stop being a victim and so close minded.

[@nft3]

I don't like this. You can't get out of Lyme/Bab/Bart by just improving yourself mentally and spiritually. That's bull. That's just an addition. You need to find medications (may be alternative) that work. That's the key and that's extremely hard. And she said nothing substantial about it.

[@aceman1969nlb]

👍❤️👍❤️. It’s not a fun ride; I know.

[@debbiejenkins4039]

Amen

[@twangel46]

I think you have M.E. I had M.E. Severely for some years, and everthing you described is like M.E. Especially cognitive effects, exhaustion, pain ( in the bones). I currently have something un diagnosed again involving exhaustion, weakness, like flu. Out ne day in bed for two. Getting worse week by week. It is not like the M.E. I had where I fainted, couldnt do anything couldnt think not evencount, eventually went dont know why.

[@Fixyourfatigue]

M.E.? She said she had Lyme disease...maybe you do too

[@cowpoke02]

west clinic looks the best place . but who knows .. doing good . here to see what ya doing . haha. thanks .

[@dreaminglifepodcast]

Been there done that.

[@anthonys5170]

Your a VIP like pearlman

[@Ego-de4dt]

Random note: her dress is HIGHLY in fashion and it’s sept 2018. But again, she is the daughter of TH

[@rdallas81]

Seen this same exact comment on another video she was on...strange

[@uke_mike]

....shit on a silver platter. I wish I had a silver platter....

[@twangel46]

Well whatever it is i hope it ever comes back

[@Fixyourfatigue]

Wtf

[@YesPlease1]

(I think they meant to say never)

[@kathleencarey3902]

I’d like her story a lot more if she wasn’t so arrogant.

[@mariellelegair]

Hmm, that’s your interpretation of her, Kathleen.

[@kathleencarey3902]

@@mariellelegair Aren't all comments here an "interpretation"? I've seen this and other interviews. Sorry, but she oozes superiority and arrogance. I want to like her, but just can't. I do appreciate her message though.

[@anthonys5170]

The # hiltons are jail birds

[@truerushblast]

Bull story i ever heard

[@bethumlas3577]

an ignorant comment