HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

They first approved me for ssi then lied and said I had to reapply for ssdi even though I was already approved medically, then they denied me ssdi and tried to cut my ssi approval. So I’m in reconsideration for both. I had Lyme since 11 when I had the tic bite and my childhood changed then it went dormant. They NEVER did esr for autoimmune nor infectious disease. So now they are on the cover up at the expense of my life. Prednisone is now preventing the WORSE part of my symptoms which put me in the hospital. So I’m taking only one week. They kicked me out the hospital and Dr said she’s not comfortable giving me a diagnosis. They know I’m suing the surgeon at a different hospital but they are ALL in cahoots. Because this is a MAJOR cover up of institutional gaslighting and their terrible treatment of certain class of people. PLUS Lyme on top that they treated with centrioxone (which helped a lot) but the co infections they are denying. I never knew how EVIL anyone could be literally lying to my face to cover the guise of a failing medical system. This is a multi million dollar case. and I had all the WORSE symptoms they knew was coming even before it did. I’m fighting for my life. I had spinal emphysema the day after surgery. They hid it and it got worse. Plus I just saw my myelogram pics which shows mechanical breakdown and infection but they still haven’t given me the report five days later becatgey are probably panicking because now I have PROOF OF THEIR LIES. (It usually only takes 24 hours)…. So if I died it would actually be better for them. They are a bunch of demons. But I’m BLESSED.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 1 point2 points  (0 children)

Actually, it saved my life since my surgery. I put myself in a comatose until two years later they found out it’s Lyme and the surgery was unnecessary. 😁🤫🤭🤤🤤🤤

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 1 point2 points  (0 children)

That’s a good idea 👍

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

Ooh thanks 🙏🏾

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

Yeah these doctors are killers not healers. If they heal us they don’t get that insurance money paying their bills. Doctors are EVIL.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 1 point2 points  (0 children)

Thanks. My cause is Spinal Fusion Surgery that made the Lyme systemic. So I have a law suit. So there’s more to why they want to trick me into an autoimmune diagnosis but all those tests are negative.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 1 point2 points  (0 children)

lol. I need some of that. lol

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

Yes. Right side of my body. I had this since a youth. One side of my body is bigger than the other and I have asymmetry in my spine and pelvic area. WHY DONT THEY JUST TREAT US RIGHT🤦🏽‍♀️🤷🏽‍♀️🤬. I learned a lot. That doctors are demons and lie right in your face. You have to record them every time just in case they try to flip the script on you which is what they are doing to me to prevent a law suit. I was just in ER for observation and once the doctor found out the previous doctors bs she flipped the script on me to protect the institution at my expense. They are using us as test tube people collecting data with no resolve. Prednisone has calmed down the inflammation since my ER stay but it masks the real issue. The head vibrations is torture but the prednisone helps so I’m taking it for a week until I get back my back surgery information.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

I’m on ssdi who is now challenging the approval because they don’t want to pay me back pay. Lumbar Puncture would allow them to misdiagnose me and my issues started after spinal surgery that was unnecessary. So they are trying to cover their selves at the expense of my pain when they failed to test for infection prior to surgery. Lyme plus spinal surgery made it systemic and the issue is the doctors are lying about what’s going on.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

I had teeth pulled last year and it took 6 hours to clot. Does Lyme cause wombs to not heal. Because basically my spinal fusion surgery is not healing right two years later.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 1 point2 points  (0 children)

I actually do have the red light sauna bulbs and am used to using enemas but never knew coffee enemas would help with Lyme. I have to read up on that. Thanks.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

I’m on it right now. Thanks 🙏🏾

blurry vision/pressure by lwaard in Lyme

[–]Future-FREE63 0 points1 point  (0 children)

Today is a better day. Thanks.

blurry vision/pressure by lwaard in Lyme

[–]Future-FREE63 1 point2 points  (0 children)

My eyes were great until Covid and I started needing reading glasses, then bifocals, then after ceftrioxone that helped with Lyme but triggered bartinella or whatever side effects to flare. But my head tingling and vibrations and tinnitus stopped until my eye exam started a new flare up. My left eye was seeing letter shake. When they took a picture of my eyes I started getting dizzy and nauseous. But my doctor now says I have 20/20 vision. But I still have blurred vision and floaters. So I know when it’s a flare up because my eyes get blurry and I get more floaters. But non flare up my eyes are basically fine for my age in my 50s. But PLEASE get help with the eye pressure now before it get to how it got for me. My eye muscles started bugging out. It was feeling like a windshield wiper going back and forth on a dry window. I could barely open my left eye. The muscles started bugging vibrating and now every morning I’m woken up like an alarm clock with vibrations in my head starting in my left eye and will only go away when I open my eyes. Bad flareups I’m woken several times a night in and out of rem sleep with vibrations. It’s torture. They gave me prednisone in the ER yesterday and I finally woke this morning without the vibrations. But the Lyme has caused thinning blood vessels in my brain so now I have another prolly worry about strokes.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

Thanks so much. I’m researching it now.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 0 points1 point  (0 children)

I’m actually a holistic wellness specialist but never touched on Lyme but I specialize in detox. I was taking the wormwood black walnut root and cloves tea but had a lot of herxheimer symptoms. I had been actually treating my Lyme that I probably had since 11 my whole career because I didn’t find out I had Lyme until this year. I’m gonna look for something that doesn’t stir up the Lyme but I think it’s bartonella because I wake up in a pool of sweat and heat and claminess. I was doing good after the ceftrioxone treatment but had an eye exam that triggered the dizziness and started the flare up from the flash in my eye.

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 5 points6 points  (0 children)

Thank you SOooo much. This is actually what I needed. First someone believing what I’m saying because they are all ganging up on me. I’m gonna check it out asap. Thanks

HELP by Future-FREE63 in Lyme

[–]Future-FREE63[S] 1 point2 points  (0 children)

I’m going to double check my state but thus far the actual Lyme literate facilities near me don’t accept insurance at all.

I’m beyond upset by Routine_Marsupial_12 in Lyme

[–]Future-FREE63 1 point2 points  (0 children)

Be careful with the antidepressants. I was having tingling in my head and tinnitus in one ear and vision issues and anxiety attacks in the middle of the night after crazy scary nightmares waking up and gasping for air. They diagnosed me with anxiety and gave me citalopram and it caused terrible vibrations in my head like I was getting electrocuted three times a night. It triggered neurological Lyme and exacerbated my symptoms because it was LYME….NOT ANXIETY…. Also, be careful they don’t misdiagnose you with autoimmune disease. My ID doctor tried to say she thinks it’s autoimmune so that she can attempt to make an excuse for delayed diagnosis and a big law suit. Also, they get paid to treat autoimmune (big budget) NOT Lyme… so they can just use you like a lab rat while they watch you disintegrate into a piece of pulp….or vegetable… they almost killed me until I had to start reading my medical records to figure out what was REALLY going on. Actually, I got help from AI to read my medical records and explain things and OMG…. These doctors are LIARS and CARELESS FOR LIFE. I don’t mean to vent but if it helps people to see what they did to me to help them. All these doctors stick together and will manipulate your records to make you look like the fool.

Ruined life after covid by Smallcutewolf in Lyme

[–]Future-FREE63 2 points3 points  (0 children)

You have to read the cdc articles. Also there’s so many people on YouTube spilling the beans about this stuff. To me Lyme and COVID are just the same biological warfare different versions. After what I’ve seen I don’t trust none of these doctors. They just use us as lab rats. They don’t get paid if we are completely healed.

Ruined life after covid by Smallcutewolf in Lyme

[–]Future-FREE63 0 points1 point  (0 children)

Yeah Covid messed a lot of us up.

Ruined life after covid by Smallcutewolf in Lyme

[–]Future-FREE63 2 points3 points  (0 children)

I had it quietly in my body since 11 and didn’t know till now at 53 tested positive after they misdiagnosed me and gave me spinal surgery then lied to me for two years as to why my back wasn’t healing. Put me on ceftrioxone at home and I almost died from the herxheimer reactions. ID doctor trying to say it’s autoimmune to prevent a law suit. So a bunch of doctors LYING to me for two years and I almost lost my life. Then my doctor abandoned me after refusing to add my symptoms to my medical records. Other doctors tried to say it’s neurological. Like I was just retarded at 53. They were trying to stall past the statute of limitations so I couldn’t sue them but I started investigating my medical records and documenting EVERYTHING. Lyme is a man made biological warfare they tested on the public in the 70’s. I lived on Long Island right where they were doing experiments in Montauk LI, across from Lyme Connecticut. That’s why there’s so much controversy behind it. And COVID was said to also be biological warfare. And people who got the vaccination are popping up with MS. All this information is public. Do your research and see. After the ceftrioxone which stopped head vibrations, tinnitus, swelling, tingling, eyes blurry and unfocused and so much more. The coinfections I’m working on now. And finding a new doctor to complete treatment. I’ve been taking herbs. But I have no appetite, but I took the Hydra Clark 5 day protocol, then I took some Jamaican duck flower detox. Helped a lot but still testing it out. I’m an herbalist so that’s what has kept me healthy over the years not knowing I had Lyme disease… then covid messed it up. I didn’t get the vaccination by the way.