Chronically Ill & Calling in Sick

[@VictoriaPearson-w1u]

One more: I belong to a support group for managing Morgellon’s…a coinfection of Lyme disease where patients are most often told we are delusional at worst- and just ignored at best. I hope you’ll talk about the trauma of seeking medical help and then not being able to find help. When one is alone and suffering in the middle of the night, it’s so hopeless feeling when you reach the point where you find you aren’t going to be taken seriously or helped, let alone even just being hear with some compassion. Thanks for your podcast! Looking forward to more.❤

[@CallingInSickPodcast]

Will absolutely be talking about this!! It's one of the hardest pillars of living with a chronic illness -- isn't it?!

[@VictoriaPearson-w1u]

Thank you for your sharing & caring! I’ve been chronically ill for more than 5 years but in the last 2 have been worse. I have autoimmune issues too and Lyme. My symptoms are almost primarily skin, nose, eyes, & ears. The torture is itching, pain, & crawling sensations. The trauma is from doctors who won’t treat this. Thanks again.

[@CallingInSickPodcast]

[@Lfs1891]

30 years with lyme disease. It's a full body form of cancer. Mimics everything, .look into alpha-gal. There's research to suggest sexually transmitted.

[@KellieDTravis]

I finally had the "spoons" to finish watching and I'm so glad I did. I loved Not So Sick Chick's and I know I'm going to love this even more. I got hurt at work as a nurse and developed CRPS. Since then, I've also developed Ankylosing Spondylitis and Inflammatory back disease. I've had a sick life also but none of that compares to this time now. Thanks for sharing your knowledge and experience with us

[@CallingInSickPodcast]

I'm so glad to hear that you loved NSSC and are loving Calling in Sick with me

[@shayminnix8618]

Your story has brought tears to my eyes. Thanks for shareing. Since 2021 ive been ill left and right but the last few months it has become constant ive been digging at drs to plz help do far nothing but im in pain all over. Ppl think im faking to just be lazy but in not i hate this. I hope your life is full of many blessings im glad i found your chanbel i feel less alone now.

[@CallingInSickPodcast]

I'm so sorry that you are in this part of the chronic illness journey... it is HARD! But I do promise it gets better. If a doctor doesn't take you seriously, then find new ones!! There are good ones that exist. Follow along on socials for more community content

[@CailaJefferson]

thank you for sharing your story, looking forward to more conversations to come!

[@CallingInSickPodcast]

So glad to have you here!!

[@clorypaola]

So excited and a beautiful intro! 🎉

[@CallingInSickPodcast]

Thank you so much!!!

[@SarahChaney]

❤ Excited to hear what is next and growing this community.

[@CallingInSickPodcast]

SO happy YOU are here and a part of this community!!

[@FollowYourBlissLife]

You're ahhhhmazing and inspiring. Best of luck.

[@CallingInSickPodcast]

Thank youuuu

[@SammanthaX345]

hearing your story reminds me a lot about myself! thank you for this podcast! i cannot wait for more!

[@CallingInSickPodcast]

I"m so glad to hear that my story resonated with you AND am sorry that it does!! Glad you found me and this podcast, and I'm here to support you

[@HollyJordan15]

Great video; thank you for sharing. I found you on Instagram. I’m from Scotland 🏴󠁧󠁢󠁳󠁣󠁴󠁿 & also am chronically ill with autoimmune nasties including MCTD; which has now been changed to undifferentiated MCTD 🙄 My son works in finance. Looking forward to watching more of your videos x

[@CallingInSickPodcast]

Sorry to hear you are in this same crummy camp, but glad to have you here

[@HollyJordan15]

@ Thank you 😊

[@kymberlymaxwelljohnson5846]

I cried listening to this. I have lupus vasculitis myofasial pain syndrome and arthritis and diabetes and copd. I wasn't believed and was basically the family disappointment because my mom and 9 older siblings thought I was lazy and a hypochondriac seeking attention. I'm an artist and I named my company Sick Chick Inc. I have friends and relatives and neighbors who think I don't need my wheelchair and that I just need to get up and exercise ect also that I don't understand the value of a dollar or that I just don't want to work and that my husband should make me do everything for myself. That since stress triggers my illness that I'm faking to avoid conflict ect ect my husband was listening and when you mentioned your affinity for softness and your spoons we both looked at each other and laughed and cried at the same time. Thank you for sharing your story because you made me feel like I'm not crazy or alone.

[@CallingInSickPodcast]

I'm so glad this helped you feel not so alone. I'm here for you!! You are doing ENOUGH, and those that do not understand and fail to show up for you do not deserve your heart

[@MissBlue8u]

❤❤❤

[@rsmithp51]

Do you have mercury amalgam fillings and or root canal feet? These can cause inflammation and autoimmune disease.

[@CallingInSickPodcast]

Nope! I have never had a cavity

[@jeffyarlett5791]

Flouride

[@greggreg2263]

Hello Snow kitten 😻

[@bubbasanches4591]

MY NAME IS GURPREET SINGH FROM INDIA 🇮🇳 I AM KHALISTAN SIKHS FROM INDIA 😊 I NEED PERMANNT RESIDENT FOR CANADA AND I CAME HERE AS STUDENT AT BRAMPTON COMMUNITY COLLEGE ITS INSIDE A VERY GOOD SHOPPING MALL 🛍 I AM STUDYIJG FOR SECURITY GUARD 💂‍♂️ PLEASE GIVE ME PERMANENT RESIDENCY I AM OWED IT BECSUSE YOUR PEOPLE IS RACIST

[@greggreg2263]

@@bubbasanches4591😘

[@setburhed4987]

Cutie

[@rsmithp51]

Root canal teeth

[@bobbylee2853]

Go Carnivore.

[@CallingInSickPodcast]

Sadly it didn't work for me :( what was your experience?