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#lymediseaseawareness

Posts tagged as #lymediseaseawareness on Instagram

62.759 Posts

Calling all mental health professionals!!! Please learn about Lyme and tick-borne disease. We need your help to assist in proper diagnoses of patients! . . #mentalhealth #anxiety #depression #lymeliteratetherapy  #psychotherapy #psychology #ptsd #learningdisability #disability #lyme #lymedisease #lymediseaseawareness #spoonie #awareness #lymeadvise #invisibledisability #lymedontkillmyvibe #strength #educate #medical #health #wellness
πŸ’š[LYME UPDATE]πŸ’š @johncaudwell is rallying the #lyme troops this weekend. Please check out his Facebook live Or Instagram live to find out more or keep reading πŸ‘‰πŸΌ”I wasn’t able to share with you precisely what my initiative is because it is embargoed until Monday morning, but suffice to say, I am really hoping that Monday’s action will be the start of a journey to change the outlook for Lyme Disease sufferers in the UK. I know you all want to know what it is I am proposing, and you will know on Monday morning but, in the meantime, it will add significant support and definitely help if you can Lobby by email your MP, with a copy to Jeremy Hunt and your local and national newspapers. Please do that this weekend, so that we gain maximum impact and traction. I know you have all written before and seen no change but, on this occasion, there is a difference. I am putting a huge amount of effort and time into a strategy that hopefully will catalyse a change for Lyme Disease sufferers. So, please please write.  I am really fighting for you.  Over the last 3 years your stories have not only touched my heart, but made me feel very angry that you are all being so dreadfully neglected.  This has to change!  I told you that 3 years ago!  I promised you that I would fight and I am fighting! I really hope that this weekend’s initiative by me will cause the Government to take notice and do the right thing but, for sure, if you all add your voice to mine it will have an even greater chance of success. To make it easier for you I have written a template letter that you can send to your MP.” πŸ™πŸ½ If you want to join the movement then please head on over to @johncaudwell Facebook page for all the links you need πŸ’šπŸ’šπŸ’š
✨ I uploaded a new video earlier ✨ This week wasn’t great, but I was kind of expecting that because of how busy the week before had been (big Lyme doctor appointment and lots of travelling). It wasn’t all bad though, I did have a couple of days where I was feeling good and managed to get quite a bit of organising done, and the days where all I could do was lie in bed the new season of Queer Eye came in very handy πŸ‘ŒπŸ» (link in bio)
🐝 Today’s sting session was BRUTAL! The summer bee stings are more painful and potent, causing a bigger reaction externally and internally. Hence, I’ve had a rough few weeks dealing with Lyme flare/herxing. BUT, I’m getting closer to #curinglymedisease with every sting! πŸ™πŸΌπŸπŸ’š ... #thankyougod #thabkyoubees #lymediseaseawareness #justkeepstinging #inthistowinthis #beevenomtherapy #bvt #fyoulyme #lymediseasesucks #miracleworkers #alwaysgrateful #myscarstellmystory #nofilter
I always love a nice poem!
#lymefacts #lymediseaseawareness
Matcha morning fact: matcha has a high concentration of chlorophyll which helps eliminate toxins from the body! πŸ’š // Recipe: 1 tsp of matcha powder 🍡, 1 scoop of @organikahealth collagen powder πŸ’ͺ🏼, 1 tbsp of @nutiva coconut butter πŸ₯₯, 1 tbsp of organic honey 🍯, 14 oz of hot (not boiling!) water πŸ’¦// blend n a high speed blender for 10-30 seconds under frothy and magical ✨ #matcha
I haven’t posted from this account in ages- but good news in in remission πŸ‘πŸ»πŸŽ‰ things are looking up my friends..- thou Lyme is a battle you never stop fighting-I’m still going to postπŸ’• Chins up everyone🐡 . . . . . . . . #lymedisease #healing #lymediseaseawareness #lymewarrior #hope #chinsup
Tomato bowl.
Susannah Cahalan may have been diagnosed with something other than Lyme, but the medical nightmare is certainly similar. This Netflix movie is not easy to watch and will hit close to home. (Lyme Madness) This powerful film gets at the core of how easy it is for doctors to check the box of mental disorders when they are not trained in recognizing inflammation in the brain. Chronic Lyme and TBDs are the Great Imitator. We must demand physician education and stop the suffering.  https://youtu.be/l3zpQo4B8Jw  #lymedisease #suicideprevention #suicideawareness #tickbornediseases #encephalopathy #gettickedoffnh #lymesuicideawareness #lymediseaseawareness #antinmdareceptorencephalitis #antinmda #brainonfire #netflix
Living in the moment is something I have learned to do with this body of mine. This picture was taken at the fair a few weeks ago, I was feeling decent, so we took advantage and jumped in the car and headed there. I was so happy walking around pain free and even danced with the kids which was an AMAZING feeling. Within literally 5 minutes my body started to shut down and I had to rush to the car in a panic. I am so grateful for the moments I do get to feel free, and my body allows me to enjoy life. I'm gratful to be alive and to have the chance to get healthy again. I am also feeling a little down, because the things that should be so easy are hard for me. I can't really make plans and I feel jipped from being able to work, having a savings, playing with my kids, just doing my part and contributing to the household. I spend so much time in pain, having to lay down with mysterious symptoms. I know it's 3 steps forward and 2 steps back in healing and I have made progress, but this last pain flare has been so hard and emotionally draining. I was feeling SO much better and then I tanked again and I felt devestated.  I just miss the freedom of being able to be spontaneous. I feel like a 33 year old trapped in a suffering body and I'm tired. I'm just so tired. I go back to Hansa in Kansas  in 2 weeks and am looking forward to continuing to get my life back and being the mom I yearn to be to my girls. Zoe prayed tonight that her mom's back would get better. She doesn't really know I'm sick, she just thinks I have a hurt back. Sending love to everyone. ❀
What is ironic about this is in 2008 my doctor told me Lyme doesn't exist in California and that it's only "an east coast thing that is very rare". Smh #lymediseaseawareness #lymedisease #cld #ticks #tbd
Did you know that not only does @yolanda.hadid have chronic Lyme but two of her three children do too! I can’t even imagine!  I have a feeling my nose will be glued to this book for the next few days! . . . #yolandahadid #believeme #believemebook #lymedisease #lymewarrior #lymediseaseawareness #spoonie #spoonielife #chroniclyme
iPhone shot taken whilst out walking at the end of winter. #winter #spring #summer #new #better #places #life #life #art #weekend #rest #clouds #light #lymedisease #lymediseaseawareness #health #gettingthere #work
https://www.facebook.com/100002075182585/posts/1800926649986490/ Im glad to see you in my info page invite your friends thanks and God Blessing #peaceandlove #bestfriend #me#beautiful #amazing #job #best #bestfriend #gift #people #peoplescreatives #help #god #peace #explore #bestfriend #peaceandlove #love #page #lupus #fibromyalgia #lymediseaseawareness #beautiful #peaceandlove #job #best .

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