[PR] Gain and Get More Likes and Followers on Instagram.

#bartonella

12492 posts

TOP POSTS

Being that #selfiecliche in #bocaraton to showcase my improvements and have a voice for all of my fellow chronically ill #SURVIVORS #lifeisworthliving or trying . Elated that I’m almost fully walking / trotting again! Ready to persevere and return to being the athlete I once was one day. My main goal round 2: is to make the cut for being a @pure_barre instructor again. NO matter how many years it takes. I can’t believe in two years the most activity my body can handle is barely a mile walk 🤬Never give up and I plan to share my treatments / journey with everyone. Know you’re not alone and remember to always take time to believe, support, and have faith within yourself. Excited to meet my new infectious dis. Team, other survivors, & my new “self”. I never thought I would be able to jump again! #lymedisease #autoimmunedisease #hashimotosdisease #multiplesclerosis #bartonella #nevergiveup #guillanbarresyndrome #survivor #limegreenfighter #ootd . Words can’t express how amazing it feels to be able to walk and feel my arms and legs again! #ootd #lifeisbeautiful #optimism #holidaymiracle 👍🏼💕🤛positivevibes.. the skater and dancer within will always prevail! Thanks to all of those who have kept my chin up and by my side in the hospital and past few years (you know who you are #talesfourthgradenothing) . I’m sorry if I haven’t responded to those who’ve reached out/ vice versa yet. Thanks everyone for everything and I promise I’ll get back to you! Thanks! #daniellesmousetrap #ootd #friday #model #bestfriendgoals #fighter

I always tell my clients it’s not about changing other people’s opinions or perspectives, it’s about protecting ourselves, building self-esteem & self-confidence, and simply - liking who you are and being proud of it vs. desiring to change it.
I’m with family this weekend, and while I love them - I’ve had some big ups and downs with them over the years. Some rough times...mostly when I was going through a lot with my own health and when I was really depressed and unhappy in my life. I often took out my pain- on them.
A lot of times I’ve felt misunderstood and unlovable - and from those experiences built up resentment.
In the last few years it’s taken a lot of effort, understanding and self-responsibility to let go and move forward. But I’ve definitely made a lot of progress.
What’s helped me the most is focusing on myself, caring about myself and loving myself instead of trying to change my family members. Because they’re them, and I’m me.
I’m sure a lot of us have a hard time around family. If you haven’t healed from the past yet, the best thing you can do is to almost put on an invisible armor when you’re with them. Protect yourself. And stand confident in who you are.
Remember everyone is just trying to do their best, with the way they view & perceive the world. We all have pasts & experiences that make us US and when you start understanding where and why people are why they are - it makes life a lot more comfortable, peaceful & supportive. The end of this year is all about letting go and moving forward. 🧡✨✌🏼

Please check out my website, www.unknownetiology.com, and let me know what you think. I posted a blog about turning 35 and being chronically ill. “I live here. This is not me passing through on my way to somewhere “better”. This isn’t a dark chapter. This is my book. And I don’t want to spend the rest of my story mourning the book I didn’t write. Couldn’t write.” #youareamiracle #lymie #lymedisease #cirs #sphincterofoddidysfunction #rarediseases #chronicillness #chronicfatigue #cfsme #millionsmissing #invisibleillness #myastheniagravis #bartonella #babesia #arthritis #misdiagnosed #bodypositive #youareloved #youareworthy #fighthard #canyouseeme #stillhere #stillhere #disabled #selfportrait #experimental #photography #myasthenic #honoryourgrief #tellyourstory @unknownetiology #singlemom

#Repost @livlymefoundation (@get_repost)
・・・Olivia speaking at the Tickborne Disease Working Group in DC. Thx @shineypink for the video. ————-............................................I’d like to take a moment to talk about inspiration. If I’ve learned one thing from this illness, it’s to believe in the power of inspiration.
In order to keep moving forward, we all need to be inspired (and someone needs to be the one to do the inspiring). Without inspirational leaders, the fighters would stop fighting and cures would never be found.
Olivia, @livlymefoundation you are that inspirational leader that this community needs! Your bravery and courage exceeds that of many adults. Keep fighting girl, you are inspiring so many of us and you are making such a huge difference!!!! The world needs more Oliva’s who aren’t afraid to stand up for millions of others and be their voice. It is leaders like you that will help us find a cure. 💚💪 #livlyme #livlymefoundation #inspiration #inspirationalleaders #sociallymeing
#lymediseasetreatment #findthepositive
#letterstolymies #lymedisease #lyme #spoonie #spooniefriends #friendshipgoals
#whenlifegivesyoulyme #lymiesunite #babesia #bartonella #lymewarrior #lymie #morethanlyme #lymestrong #fightlyme #lymedontkillmyvibe #neurologicallyme

Please check out my website, www.unknownetiology.com, and let me know what you think. I posted a blog about turning 35 and being chronically ill. “I live here. This is not me passing through on my way to somewhere “better”. This isn’t a dark chapter. This is my book. And I don’t want to spend the rest of my story mourning the book I didn’t write. Couldn’t write.” #youareamiracle #lymie #lymedisease #cirs #sphincterofoddidysfunction #rarediseases #chronicillness #chronicfatigue #cfsme #millionsmissing #invisibleillness #myastheniagravis #bartonella #babesia #arthritis #misdiagnosed #bodypositive #youareloved #youareworthy #fighthard #canyouseeme #stillhere #stillhere #disabled #selfportrait #experimental #photography #myasthenic #honoryourgrief #tellyourstory @unknownetiology #singlemom

SRT Energy Enhancement (Sympathetic Resonance Technology)

Based on the knowledge that every physical system has fields of energy that permeate and surround them. When our frequency vibrates at their optimal levels, we are able to function more efficiently and properly.
Who am I these days? Over the last 3.5 years, I have changed a lot and have witnessed & experienced the power of alternative modalities. It’s been an interesting journey to say the least! Holding onto hope for complete healing!
#lymedisease #chronicillness #chronicpain #fibromyalgia #chronicfatiguesyndrome #mycoplasma #bartonella #babesia #SRT #alternativemedicine

MOST RECENT

Being that #selfiecliche in #bocaraton to showcase my improvements and have a voice for all of my fellow chronically ill #SURVIVORS #lifeisworthliving or trying . Elated that I’m almost fully walking / trotting again! Ready to persevere and return to being the athlete I once was one day. My main goal round 2: is to make the cut for being a @pure_barre instructor again. NO matter how many years it takes. I can’t believe in two years the most activity my body can handle is barely a mile walk 🤬Never give up and I plan to share my treatments / journey with everyone. Know you’re not alone and remember to always take time to believe, support, and have faith within yourself. Excited to meet my new infectious dis. Team, other survivors, & my new “self”. I never thought I would be able to jump again! #lymedisease #autoimmunedisease #hashimotosdisease #multiplesclerosis #bartonella #nevergiveup #guillanbarresyndrome #survivor #limegreenfighter #ootd . Words can’t express how amazing it feels to be able to walk and feel my arms and legs again! #ootd #lifeisbeautiful #optimism #holidaymiracle 👍🏼💕🤛positivevibes.. the skater and dancer within will always prevail! Thanks to all of those who have kept my chin up and by my side in the hospital and past few years (you know who you are #talesfourthgradenothing) . I’m sorry if I haven’t responded to those who’ve reached out/ vice versa yet. Thanks everyone for everything and I promise I’ll get back to you! Thanks! #daniellesmousetrap #ootd #friday #model #bestfriendgoals #fighter

Please check out my website, www.unknownetiology.com, and let me know what you think. I posted a blog about turning 35 and being chronically ill. “I live here. This is not me passing through on my way to somewhere “better”. This isn’t a dark chapter. This is my book. And I don’t want to spend the rest of my story mourning the book I didn’t write. Couldn’t write.” #youareamiracle #lymie #lymedisease #cirs #sphincterofoddidysfunction #rarediseases #chronicillness #chronicfatigue #cfsme #millionsmissing #invisibleillness #myastheniagravis #bartonella #babesia #arthritis #misdiagnosed #bodypositive #youareloved #youareworthy #fighthard #canyouseeme #stillhere #stillhere #disabled #selfportrait #experimental #photography #myasthenic #honoryourgrief #tellyourstory @unknownetiology #singlemom

Please check out my website, www.unknownetiology.com, and let me know what you think. I posted a blog about turning 35 and being chronically ill. “I live here. This is not me passing through on my way to somewhere “better”. This isn’t a dark chapter. This is my book. And I don’t want to spend the rest of my story mourning the book I didn’t write. Couldn’t write.” #youareamiracle #lymie #lymedisease #cirs #sphincterofoddidysfunction #rarediseases #chronicillness #chronicfatigue #cfsme #millionsmissing #invisibleillness #myastheniagravis #bartonella #babesia #arthritis #misdiagnosed #bodypositive #youareloved #youareworthy #fighthard #canyouseeme #stillhere #stillhere #disabled #selfportrait #experimental #photography #myasthenic #honoryourgrief #tellyourstory @unknownetiology #singlemom

#Repost @livlymefoundation (@get_repost)
・・・Olivia speaking at the Tickborne Disease Working Group in DC. Thx @shineypink for the video. ————-............................................I’d like to take a moment to talk about inspiration. If I’ve learned one thing from this illness, it’s to believe in the power of inspiration.
In order to keep moving forward, we all need to be inspired (and someone needs to be the one to do the inspiring). Without inspirational leaders, the fighters would stop fighting and cures would never be found.
Olivia, @livlymefoundation you are that inspirational leader that this community needs! Your bravery and courage exceeds that of many adults. Keep fighting girl, you are inspiring so many of us and you are making such a huge difference!!!! The world needs more Oliva’s who aren’t afraid to stand up for millions of others and be their voice. It is leaders like you that will help us find a cure. 💚💪 #livlyme #livlymefoundation #inspiration #inspirationalleaders #sociallymeing
#lymediseasetreatment #findthepositive
#letterstolymies #lymedisease #lyme #spoonie #spooniefriends #friendshipgoals
#whenlifegivesyoulyme #lymiesunite #babesia #bartonella #lymewarrior #lymie #morethanlyme #lymestrong #fightlyme #lymedontkillmyvibe #neurologicallyme

A great recipe that saves time and spoons ;) !!!! - After a long day of traveling, it’s nice to come home to pre-prepped #glutenfree #dairyfree #soyfree #lowhistamine #lymediet friendly food.

On Wednesday I baked turkey cutlets in foil and then froze them so I had minimal work to do after my ozone treatment this week (thinking cap – on!) The process is super easy – just take out the turkey cutlets, toss on any seasonings that you want. I left mine plain.

Drizzle 1 tsp of olive oil on each cutlet and close-up foil.

Bake in oven on 400 for 15-20 minutes (until no longer pink- cooking time depends on cutlet thickness, mine were thin). When the turkey packets are cool, I open the foil and flip the cutlets (so it continues to soak up juices). Then, I pop them in the freezer (freezing immediately after cooking stops histamine production). Note: I’ve done this with chicken too, it’s a great way to keep poultry moist with minimal prep and effort!

When I got home today, I tossed a foil packet in the oven and sautéed some zucchini with pink himalyan salt and 1 tsp olive oil. When the turkey defrosted, I sautéed it with the zucchini and another tsp of olive oil. It was a great way to have a quick and delicious lunch!

Note: I have a lot of allergies and intolerances right now, so I cook very plain. If I had a say.. I would have added fresh rosemary to the turkey cutlets before baking. I would also suggest to sauté some garlic and fresh rosemary with the zucchini and turkey.

I’m constantly experimenting with ideas on how to work smarter, not harder.... How do you guys make food prep easier?! Please share 🤗. #foodprep #glutenfree #dairyfree #soyfree #lowhistamine #cleaneating #lowhistamine #gaps #paleo #aip
#lymediseasetreatment #findthepositive
#sociallymeing #letterstolymies #social #lymedisease #lyme #spoonie
#whenlifegivesyoulyme #lymiesunite #babesia #bartonella #lymewarrior #lymie #seziures #morethanlyme #lymestrong #justkeepswimming #lymedontkillmyvibe #neurologicallyme

Lyme disease makes me so tired. 😴😥😴. Eye lids feel heavy, muscles feel heavy, head feels full and dizzy. Watching family decorate tree but I'm too tired. I need to start up my herbal remedies again but I feel too tired to begin the process again. I need to remember how far I'v come, but it just feels so endless sometimes. Keep fighting everyone we'll get there 💚😴💪🌲❄️. #lymedisease #lyme #chroniclyme #chronicillness #chronicpain #chronicfatigue #sotired #babesia #bartonella #curelyme #curecdc #cureidsa #fibromyalgia #backpain #pots #onebite #onebody #spoonies #fighter #sicklife #lymewarrior #butyoudontlooksick #prayer #invisibleillness #strength #💚

Nothing like a little #amphotericinb cocktail up your nose in the morning (and the evening.) I was on a similar sinus protocol anti-biotic combo for seven months to treat mold and #marcons and they failed. Then my #llmd didn't address it for six months and now he's like oh yea you need to go back on this for... two to three years. I'm going to an ENT in January for a second opinion but for now I have to be on this because I've been barely able to breathe lately. Thanks, bro. Gotta love the crazy expensive compounded meds (which us #lymewarrior folks know all too well especially when they fail and you start again.) #herxmas #mold #lymediseaseawareness #lymedisease #chronicillness #spooniestrong #lymestrong #babesia #bartonella #lymedisease #recovery #meds #literallymoney #justkeepswimming

SRT Energy Enhancement (Sympathetic Resonance Technology)

Based on the knowledge that every physical system has fields of energy that permeate and surround them. When our frequency vibrates at their optimal levels, we are able to function more efficiently and properly.
Who am I these days? Over the last 3.5 years, I have changed a lot and have witnessed & experienced the power of alternative modalities. It’s been an interesting journey to say the least! Holding onto hope for complete healing!
#lymedisease #chronicillness #chronicpain #fibromyalgia #chronicfatiguesyndrome #mycoplasma #bartonella #babesia #SRT #alternativemedicine

Keep calm and peppermint on!! I love this essential oil necklace. The wood holds the essential oil of your choice and it can be smelled for hours! Peppermint has been my favorite oil lately, it’s calming and great for headaches! I got this one at a local store called #wildbynaturemarket @wildbynaturemarket on Long Island.. but there are also a lot of options online if you google “essential oil necklaces” you will find a bunch of options! What’s your favorite essential oil or your favorite way to get your aromatherapy in?! #aromatherapy #peppermintoil #essentialoils #calming
#lymediseasetreatment #findthepositive
#sociallymeing #letterstolymies #social #lymedisease #lyme #friends #spoonie #spooniefriends #warrior #friendshipgoals
#whenlifegivesyoulyme #lymiesunite #babesia #ehrlichia #bartonella #ebv #lymewarrior #lymie #morethanlyme #lymestrong #justkeepswimming #fightlyme #lymedontkillmyvibe

😷💉Friday last week.. Day 3 of IV treatment, things started to go downhill from here. I was able to do 1 more IV session the next day, Saturday 9th Dec, then my Dr canceled the last half of my IV sessions as I got way too sick as the infections are extremely active & flaring up too many symptoms(loss of feeling in legs, slurred speech, heart palps & tachycardia, POTS, collapsed, stabbing pains thoughout my body, migraines..just to name a few). I've also tested positive & relapsed to another infection so that explains alot!! 😠😠😠😣😣😣
I have a new game plan/treatment protocol now though with oral antibiotics, herbal medicine, supplements & vitamins. Started this on Tuesday so wish me luck on continuing to kick these vector-borne infections ASSES!!! #FriYay #Bartonella #Babesia #VectorborneDiseases #InvisibleIllness #SmileThroughTheBullshit ✊ Well I try... :(

I always tell my clients it’s not about changing other people’s opinions or perspectives, it’s about protecting ourselves, building self-esteem & self-confidence, and simply - liking who you are and being proud of it vs. desiring to change it.
I’m with family this weekend, and while I love them - I’ve had some big ups and downs with them over the years. Some rough times...mostly when I was going through a lot with my own health and when I was really depressed and unhappy in my life. I often took out my pain- on them.
A lot of times I’ve felt misunderstood and unlovable - and from those experiences built up resentment.
In the last few years it’s taken a lot of effort, understanding and self-responsibility to let go and move forward. But I’ve definitely made a lot of progress.
What’s helped me the most is focusing on myself, caring about myself and loving myself instead of trying to change my family members. Because they’re them, and I’m me.
I’m sure a lot of us have a hard time around family. If you haven’t healed from the past yet, the best thing you can do is to almost put on an invisible armor when you’re with them. Protect yourself. And stand confident in who you are.
Remember everyone is just trying to do their best, with the way they view & perceive the world. We all have pasts & experiences that make us US and when you start understanding where and why people are why they are - it makes life a lot more comfortable, peaceful & supportive. The end of this year is all about letting go and moving forward. 🧡✨✌🏼

I used to be super scared to post pictures without makeup when I was glowing and healthy looking let alone.... sick?!! Fogettaboutit. 😂Real talk though - without makeup the tiredness is apparent and that's how it is right now, that's the truth so why should I be embarrassed or ashamed? I just have to laugh sometimes. How much power am I gonna give to dark circles under my eyes? 😂Does being sick or looking sick make me less valuable or worthy of love? No. after a lifetime of body image struggles this humbling journey is forcing me to practice radical self acceptance. The key word is *practice* - it's not perfect and never will be, but I keep trying. Do I still get into head trips about this stuff? Yes!!! but I also have the tools and willingness today not to stay in them too long. I still struggle a lot but this is the most I have ever accepted myself as I am. It's amazing that a painful journey can also show you beautiful things like that it is MORE than ok to be ok with yourself especially when things are far from ideal. When the going gets rough, we need self compassion most of all. I hope someone else sees this and realizes the same thing about themselves. Self love is self care. I had my son all day today and after three days at the dentist and lyme and sibo flare happening it was a one minute at a time kind of day. But I am grateful for my time with him even though it's hard right now. being his mom keeps me going sometimes, he reminds me how important it is to keep fighting even when it feels like I can't. 💚

#lymemom #chronicillness #spooniemom #spooniestrong #odaat #selflove #acceptance #recovery #tickborneillness #lymediseaseawareness #keeptrying #hope #nevergiveup #justkeepswimming #congenitallyme #babesia #bartonella #flare #almostfriday #lymedisease #lymewarrior #pots #cfsme #fibromyalgia

Sitting at dinner tonight and Bart hands struck! Veins bulging, hands on fire and blood red, fingers swollen like ball park franks 🔥 not to mention my nails gnawed to the quick from out the roof anxiety the last several months! #lymedisease #imalljackedup #bartonella

Half of today's bags full of hell... back in action at 1/4 the dosage from last year when I finished treatment. Feeling ill like I've never felt before, which means the next month is going to be a challenge and we are trying to figure out why this is happening so fast and at such an extreme. I'm going to be sharing a lot more this round because I feel that sharing reality helps people become more aware of just how serious Lyme and co-infections can be- and it can happen to anyone at anytime. No one is immune, but early detection and treatment can prevent what has happened to me. Just keep swimming Carly, just keep swimming.... #lymedisease #dysautonomia #gastroparesis #babesia #bartonella #epsteinbarr #cytomegalovirus #immunedeficiency #pots #infectiousdisease #superinfection #allfromatinybugbite

Doing the hard work detoxing in my hyperbaric chamber. Sometimes it’s hard just to get motivated to do treatment of any kind… ♿️🐾Find us on YouTube: Slice of Lyme, for daily vlogs showing life with Chronic Lyme Disease & the help of one amazing servicesdog!♿️🐕
#sliceoflymevlog
#sliceoflymevlogyoutube
#servicedogvela #dutchshepherd
#servicedogsofig
#psychiatricservicedog
#mobilitydog
#tasktraining
#chroniclymedisease #lymedisease #chroniclyme #lyme #lymewarrior #chronicillness #borrelia #bartonella #babesia #micoplasma #marcons #mastcellactivationdisorder #POTS #fibromyalgia #endometriosis
#chronicfatigue #IBS #vestibularmigraines
#irlensyndrome #mastcellactivationdisorder #MCAD #hyperbaricchamber #oxygentherapy

The sight after a long day in the clinic. I never thought I would know what it feels like to be a “sick person” .. you know what I mean the people that are on the movies and get sick with cancer and have to get IVs and fight for their life and stuff. I never saw that as a possibility, even though I myself have been in and out of hospitals my whole life and have never really been well... I never imagined it. Sometimes illness is isolating and lonely but you can’t stay in that place, but it’s okay to know it’s there. A space people like me all know very well but avoid to the best of our abilities and when we see one of our own falling into the pit of despair or loneliness we reach out our hands and stop them. Because no one should live in that space. No one deserves to be lonely, afraid, or isolated from the outside world; the people in it; and the things you used to love to do. We all deserve to be in a good space, where we are loved and truly cared for. @envita_medical_centers has been that for me, and not only me—my boyfriend and family and fellow patients too. The clinic itself is healing but the patients themselves have so much wisdom to share and love to give. I’m so thankful to have this view at the end of my day because without everyone helping fundraise and support us, I wouldn’t have the opportunity to even give this disease a fighting chance. Thank you. #iwillwin #thisdiseasewontbreakme #lymewarrior #toughwoman #bartonella #candidasucks #stomponborrelia #family #thankful #blessed🙏

Truth lol 🤣

I've gotten the rx factor down a lot over the past year;mostly supplements and herbal. Babesia is gone, but still more battles to fight. Every time I get bed bound, I think it's worse than the last,but seems like it's similar levels of discomfort but spread around my body differently. 'Gotta say,this sucks...if there were sucking to be done on the moon,this would be there,but I handle it better now,at least for now.

Be confused, it’s where you begin to learn new things. Be broken, it’s where you begin to heal. Be frustrated, it’s where you start to make more authentic decisions. Be sad, because if we are brave enough we can hear our heart’s wisdom through it.
Be whatever you are right now. No more hiding. You are worthy. ALWAYS. -S.C. Lourie 💪🏻💚
#lymiemomma #lymiemommaofirishtwins #lymedisease #lymediseaseawareness #chroniclyme #babesia #bartonella #gastroparesis #fibromyalgia #neuropathy #chronicmigraines #hypoglycemia #degenerativediscdisease #pcos #tattooedmomma #tattooedgirls #momswithink #momswithtattoos #momsofinstagram #girlswithink #girlswithtattoos #girlswithglasses #girlsofinsta #mtsm #singlemom #snapchat

Meet my travel buddies: Senior Croc Pot and the Brave Little toaster! I would like to take a moment to thank Lyme for making me use my noodle to think outside of the box... That’s right people... I did bring my own crock pot and toaster oven to the hotel 😂. When your diet is so restricted you learn to travel smart so you can eat!
Tomorrow is ozone round 2! Here’s to getting back some more brain cells and killing off some spirochetes!! What do you guys do or bring on your travels that makes life a bit easier?! #criticalthinkingskills #winning
#imathinker #findthefunny #findthepositive
#sociallymeing #letterstolymies #social #lymedisease #lyme #friends #spoonie #spooniefriends #warrior #friendshipgoals
#whenlifegivesyoulyme #lymiesunite #babesia #ehrlichia #bartonella #ebv #lymewarrior #lymie #morethanlyme #lymestrong #justkeepswimming #fightlyme #ozone #lymedontkillmyvibe #neurologicallyme

🙌

I woke up crying and immediately felt compelled to watch @ladygaga #perfectillusion After having seen her documentary #fivefoottwo I have such a deeper respect and perspective for her but also watching this video. It PAINS me to not be able to use my body this way anymore. It’s like a death. If I ever get my body back.... you can find me deep in the desert dancing my heart out in the dirt.... and no not at some dumb trendy douche festival... I miss the way you moved, body. I miss how we became one, with the music, body. I miss feeling that freedom, body. We used to be a good team, body. I’m so fucking mad that you have betrayed me, body. Something I loved and I lived so hard that came from my heart and from my soul. I truly felt dancing was such a gift. To have that gift stripped away from me.... What else more can i lose? I’ve lost so much. I’ve lost everything but my life. And I’m not living. This is sheer survival mode. Whether it’s this life or in another, I know I’ll be dancing again. I’ve always said that my concept of heaven is whatever I want it to be. And for me..... it’s dancing on a desert dance floor for eternity. #chronicillness #chronicpain #chroniclymedisease #neurologicallymedisease #lymedisease #bartonella #babesia #dance #dancers #meetmeonthedancefloor #ladygaga #depression

It's time to detox. I've been feeling really good for the past 3 weeks. I've been herxing some, especially from the bartonella tincture. I've been acting more like a "normal person". For the last year, I laid in bed. I didn't have the energy to move, my arthritis was terrible. I was also in a BIG depression. I didn't realize I was so depressed. Lyme can really get to your head. I'm always here if anyone needs to talk. I wasn't stable to ask for help. Things are better. I'm almost scared to tell you guys I'm feeling better (from Lyme and depression). But today, I'm sitting on the bathroom floor writing this. I'm so tired, in pain, mostly my legs. My lyme neck pain is back, and my hands are so numb. I don't know if it's just a die off. Tomorrow is a new day. I don't detox enough. I guess it's time. 💦🚿🛀
#lymedisease #lyme #bartonella #mcas #lymedontkillmyvibe #lymewarrior #depression

Detox like a MTHFR 🤗 You know you’re chronically ill when you ask for detox support for your birthday 😂 my birthday isn’t until Sunday but my parents thought it’d be silly to leave it sitting around when I could be getting use out of it 😊

Attempted another session at the gym tonight. When my body can handle it I try to pretty much do physical therapy. So tonight I've decided on a little reading, and an #epsomsalt #bath. Thankfully more of my new medication #lowdosenaltrexone came today so I'll be back on my regular schedule to weening off my arthritis medication for it. Although it's not totally improving my pain levels, spasms or fatigue. It has improved it by a small percentage. So I'll take what I can get. #lymedontkillmyvibe #lymedisease #arthritis #babesia #bartonella #newread #gym #physicaltherapy #instagood

Today was way worse than yesterday for some reason at the dentist. Different technique with a different person. I had an unusual amount of bleeding. Laser is done and deep cleaning is done though and I'll be back in a month for just a normal cleaning. I've been told I have the gums of someone in their seventies at 27. I have barely any enamel left. I don't eat sugar, I floss and brush with an electric toothbrush twice a day. I do what I am supposed to do but anemia, lyme, and thyroid issues that won't heal because of lyme do things I can't control. Until two years ago I had never had any problems with my teeth. Immunocompromise wears a body down. I was taking ten minute walks again for awhile but the last month I have been declining again and the last few weeks it's been a struggle to move and get through my days with my son. I am powering through life and what needs to get done but it's a challenge. I miss the days when everything I did wasn't a struggle but this is where I am right now. Times are tough but I am tougher and I'm not ready to give up. I so miss being well or at least being able to take a deep breathe with ease, get through my day without every step being calculated, having to rest after anything that happens in my day and often not being able to and that being difficult as well. I want vitality but I am fighting for it. I'm so grateful for all the wonderful supportive spoonies on here. Wishing you all only healing and peace. One day at a time. We are doing the best we can and our best is good enough. #spooniestrong #chronicillness #lymediseaseawareness #lymedisease #dentalhealth #babesia #anemia #bartonella #tickborneillness #lymewarrior #spoonielife #lymedontkillmyvibe #hope #nevergiveup #keepgoing

Persistence is key. I'm really, really struggling physically. It's been set back after set back this year but I'm not giving up. I do believe that anything is possible. In 2018 I have a goal find a better path to wellness as I haven't had much success with the treatments at my current #llmd. I may not be well by the end of that year either, but I will still be well on my way. I'll be closer to wellness than I am now. This journey eventually has to end, they all do. Never give up. #lymedisease #chronicillness #odaat #justkeepswimming #hope #tickborneillness #babesia #bartonella #lymeisreal #lymeishell #spooniestrong #lymestrong #lymewarrior #letgoletgod

Most Popular Instagram Hashtags