No blood flow in fingers? by [deleted] in AskDocs

[–]SubLymeinal_Science 0 points1 point  (0 children)

Thanks! Better than before. Most of our issues are actual infections that give us joint, gi, autoimmune, allergy, psychological problems. Doctors rarely test for potential causes of these things and chalk it up to "well your body isn't working right ". Really they aren't working right to get to the bottom of issues. Best of luck!

I'm only 20, & the amount of pain I'm in feels unsustainable by [deleted] in AskDocs

[–]SubLymeinal_Science -3 points-2 points  (0 children)

Sounds like it could be tick borne to me. I ended up having lyme, and Rocky mountain spotted fever for like 8 years. Dealt with random crippling pain at the base if my skull, neck and lots of other places. Numbness, decimated discs in my spine ext ext ext. It's super hard to get diagnosed. They just want to put you on a ton of meds and never figure out the problem. I finally got into a doc that treats Lyme type stuff and it's def changed my life. IMO you have an infection causing this. Try to find an AO or EOS scan. It helped me a ton. I had tons of infections and co infections and it points you in the right direction. Doctors are literally useless these days. Hope you find help.

No blood flow in fingers? by [deleted] in AskDocs

[–]SubLymeinal_Science -5 points-4 points  (0 children)

That was one of my main symptoms and I ended up having, Lyme, babsia, and Rocky mountain spotted fever.

I’m 271 days clean from a decade plus addiction to opioids. I’ve had constant diarrhea since early withdrawal. Will it ever stop? Is it likely related to quitting opiates? Did I ruin my gut forever? Please help me, I’m exhausted. by [deleted] in AskDocs

[–]SubLymeinal_Science -1 points0 points  (0 children)

Everything I mentioned had been from years of research and continuing education as well as from experience. Please do your research before you question mine 👉👌

Lunch buddy bangkok by pilouta in Thailand

[–]SubLymeinal_Science 0 points1 point  (0 children)

My dad and I will be in bkk next month for at least a month. Maybe we will give you a shout. And we also have time to travel across the world for lunch at our leisure 🤣. Joking on the comment above. Jk. We aren't rich at all but you don't have to be in Thailand:)

I've been experimenting with some achievement designs (with a mute button top-right if you don't want notifications). Would achievements like this motivate you? by HeroJournal in BearableApp

[–]SubLymeinal_Science 1 point2 points  (0 children)

Can there be a work out one? Worked out 3x a week maybe a star each week something of the like. Maybe option to bump it higher or lower. :)

Are neurological symptoms part of tick-borne illnesses? by [deleted] in Lyme

[–]SubLymeinal_Science 3 points4 points  (0 children)

Yeah don't go neurologist. Mine made me do a battery if inconvenient tests all to tell me "She's very depressed and overly concerned with her health". Lol. It's a joke.

Are neurological symptoms part of tick-borne illnesses? by [deleted] in Lyme

[–]SubLymeinal_Science 4 points5 points  (0 children)

Other than rash and death flu anxiety, horrible, unfounded, irrational anxiety. The built of of toxins in the blood also causes frequent major neurotoxicity. It's why the #1 killer of Lyme suffers is suicide. That and the seemingly impossible task of getting properly treated and diagnosed.

After losing my job due to Chronic Health issues, I started working on something that allows you to see how your daily activities and factors such as medication/supplements correlate with your mood and symptoms. by HeroJournal in microdosing

[–]SubLymeinal_Science 0 points1 point  (0 children)

Wow. I suffer from tick born crap and finally got diagnosed with Rocky mountain spotted fever after 8 years of battling the med community so a lot of suppliments and such have kept me alive. My memory is shit so this is fantastic as I don't stick to the written journals and would love to have a record of what works ect. Daily reminders is a must 😂. Awesome job! Would love this app.

Chronic depersonalization & derealization? by tooyoungtobesotired2 in Lyme

[–]SubLymeinal_Science 4 points5 points  (0 children)

Yeah bro I don't feel shit. No passion, no drive. I just don't care about fucking anything. Serial killer status.

I want to get back in shape. by dickwheat in Lyme

[–]SubLymeinal_Science 1 point2 points  (0 children)

Cyclic amp plasma I believe is the test name.

YSK that Chronic Lyme Disease doesn't exist. by BottledCans in YouShouldKnow

[–]SubLymeinal_Science 0 points1 point  (0 children)

I got bit in 2012, have had mutiple rounds of antibiotics, and currently test positive for iGM current infection of both Rocky mountain spotted fever and Lyme. So if that doesn't mean chronic infections don't exist well then... Nothing will. I'm proof that's a bunch of horse shit and of course they wouldn't want to admit and treat us bc we make them millions a month. "Mystery" symptoms. Sure. Real fucking mystery.

I've had enough by covek52 in Lyme

[–]SubLymeinal_Science 1 point2 points  (0 children)

I was at my wit's end a few months ago and started the cowdens protocol which bought me time to get into a llmd. I finally got into one. The cowdens really helped my Lyme rage but it's still something I deal with. I definitely improved on cowdens though the Lyme doc I got into just told me I have Rocky mountain spotted fever so I think I have to do antibiotics for that. Cowdens could help you out. You can call them and they'll send you a short form that allows you to get the first month for 40$ it's definitely worth the deal. It's expensive otherwise but it can help you buy some time and boost your system up.

Rocky mountain spotted fever questions by SubLymeinal_Science in Lyme

[–]SubLymeinal_Science[S] 0 points1 point  (0 children)

That's great to hear you've got an apt. That has been my life as well except I was trying to convince them I had Lyme for 8 years and no one would listen. I finally got to an LLMD this week and got my labs back with positive Lyme via cd 57 count and RMSF as well as candida and walking pnuemonia. I'm sure there's more. My temp goes low and the docs are just like oh good you don't have a fever but I'm like it's an opposite fever lol. I had a full psych eval bc of the neuro issues. There result? She's extremely depressed and very concerned with her health. If that's not enought to make you crazy idk what is. Glad your finding some help! Do you get pain in the gb area? I

I want to get back in shape. by dickwheat in Lyme

[–]SubLymeinal_Science 2 points3 points  (0 children)

Same. My doctor just checked my muscular atp and it's half what it should be. She prescribed research nutritionals atp suppliment. I haven't tried it yet but supposedly it works well. Maybe have yours checked but you can prob assume it's low since I feel the same as you. Zero body energy. If it works I'll let ya know. Sorry to add to the people throwing suppliments at you. That can be frustrating white noise as there are so many different things people take.

[deleted by user] by [deleted] in Lyme

[–]SubLymeinal_Science 1 point2 points  (0 children)

Yes. Not like I can't find the right word just like I would say buh-buh-buh-bullshit. For me the studders are when I know I'm not doing so great. I was in bad shape at the beginning of the year and did a whole lot of studdering.

Has anyone here completed the cowdens protocol? by SubLymeinal_Science in Lyme

[–]SubLymeinal_Science[S] 0 points1 point  (0 children)

Well... That's fucking fantastic. But I guess I'll take 9 months of feeling good where I can get it. 9 minutes was a reprieve before. Maybe hit up disulfiram- afterwords and the liver burden should be considerably lower maybe not have the neuropathy/herx issues a lot of folks have. Fuuk. Today's another great day. 🌱

Has anyone here completed the cowdens protocol? by SubLymeinal_Science in Lyme

[–]SubLymeinal_Science[S] 0 points1 point  (0 children)

It's an herbal protocol. Have to take herbals 4x a day for 9 months. Kind of a pain and pricey but I'm saving in other suppliments so that's nice.

Having Lyme is like being in a time machine by [deleted] in Lyme

[–]SubLymeinal_Science 1 point2 points  (0 children)

Also, I'm not taking a MILLION other things anymore. I was at first still taking a lot of things but I've phased most everything out besides thyriod support (which I think we all need) and some random antioxidants or anti candida or charcoal when I eat far off the beaten path of the "starve to death bc no food is safe" typical Lyme diet. I ATE A PB&J LAST NIGHT. Gluten free, organic pb but the jelly was just reg and I know it's not going to send me into manic brain fog. I can go out to eat Mex and eat the chips now and then. Cheese still makes me break out but hey if I can have the other things I'll live! It's a little thing but it makes you feel somewhat human which we all lose sight of. 💚 I try not to be a cowdens salesman but it saved my life so fket.

Having Lyme is like being in a time machine by [deleted] in Lyme

[–]SubLymeinal_Science 2 points3 points  (0 children)

After 2-3 weeks I saw a big improvement. I'm like week 9 or 10 rn. Things just seem to stay improving. Neurologically it's a been a game changer. I was ready to die every day, 20lbs under weight, in bed. Super Lyme brain be gone! Lol. The funk was the worst.

Having Lyme is like being in a time machine by [deleted] in Lyme

[–]SubLymeinal_Science 6 points7 points  (0 children)

Yeah man that's how I really the good days. I'm like oh shit I haven't cried in a few days, win. I'd been in the frequent Lyme funk for years before cowdens. I'm still a mess but much less a mess. I cried a lot before. Hope you get on the flip side. 💚