So glad to learn of this forum as I am not on any social media sites! I have developed a significant rash that started a few months ago as little itchy red bumps, and it has now spread to both of my hands, arms and legs. I saw a dermatologist a few weeks ago and was told that she is seeing it, doesn’t know what it is, but I was put on a steroid taper and a topical steroid. The rash didn’t worsen during that time but since has continued to spread. It itches like a bad case of poison oak and I have not found a topical agent that gives more than a short time of relief. Benadryl has become my nighttime friend.
I have gone through the FLCCC protocol for mast cell activation syndrome (two weeks) but have not had any relief. The only thing that has changed in my life in the last four years has been receiving the initial Pfizer series in 12/20 & 1/21. I work in a hospital so of course we all “had” to have the shots. I looked up my lot number on “how bad is my batch” and it is one of the bad ones, not the worst but still way up on the list that was one of the batches delivered to my hospital. I have listened to Dr. McCullough indicate that we are probably now going to be looking at autoimmune disorders and cancer so of course I can’t help but wonder if this whole thing is related. I am 62, have always been very healthy, eat an organic diet that is very focused on the alkaline side, have no family history of autoimmune disorders. I am waiting for some lab results and see my dermatologist this week for hopefully a biopsy as it is so much worse than my first visit.
I wonder if there is anyone out there that has seen or experienced this, or knows of a provider who may be in the Southern Oregon area or via telemedicine that can help me get to the bottom of this. The last picture is what it looked like less than a month ago and the other ones are current. Thanks to anyone who can help me out.
Hi again. I also remembered this comment from Corrie (also depicts one of the cases) under Dr Kory’s substack articles on shedding. She has developed mast cell activation and Cutaneous T cell lymphoma (sounds horrific and sending love and compassion as you wait a diagnosis - Cutaneous T-cell lymphoma: Symptoms, Classification, and Treatment - DermNet). Have you checked out the telemedicine available from FLCCC. I can’t access it from Australia.
Hi Bluebird – Welcome to the community!
Which parts of the MCAS protocol have you tried? Assuming you are using the protocol on page 22 of the I-RECOVER Post Vaccine protocol?
Did you see there is a new low histamine guide?
And a histamine intolerance food infographic? https://imahealth.org/wp-content/uploads/2024/03/FLCCC-Histamine-Intolerance-Yes-No-Foods-min.pdf
If it is coming from mast cell issues – they are tricky to treat and it takes a lot of trial and error to figure out what your triggers are. I’m not a doctor, just a mom with a young adult daughter who has had severe MCAS since she was in her mid teens. For her, it takes a low histamine diet + ketotifen + quercitin + cromolyn + hydroxyzine to keep her reasonably controlled.
Think if it were me, I would also be doing the post vax protocol with the nattokinase, bromelein & curcumin (and if I had to choose one thing to start with it would be the nattokinase).
Check out the FLCCC provider directory if you’re looking for someone to help treat:
Don’t overlook providers who are out of your state but do Telehealth. Know that Dr. Kory’s clinic (https://drpierrekory.com/) does. Also folks like Dr. Mollie James (https://jamesclinic.com/) – she is in MO but her team does telehealth for people in many other states.
I have to qualify my comments by explaining that I have no experience with the “vaccines” ~ However, I can attest to the fact that an Epsom salt soak can help immensely with pain and itching:
I would also strongly recommend utilizing the FLCCC’s post vax protocol.
In addition, there is considerable evidence linking skin issues with gut issues, and the spike protein is known to wreak havoc in the gut. For this reason, any work you do to help heal your gut may also help with skin issues:
Thank you so much!
Sorry for the delayed response. I have been on the H1 & H2 blockers as well as cromolyn, an antihistamine diet, and of course the supplements and Ivermectin. So far nothing seems to touch it and today I had labs come back that indicate I have an autoimmune disorder, so more diagnostics ahead. But I so appreciate your kind response!
Wow, you have been through a lot. I had lab work returned today that is pointing towards an autoimmune disorder but I have to see rheumatology to determine what exactly. I am already on so much of the FLCCC protocol as well as the Spike Support for several months, but this is a fairly new issue and I haven’t had relief. We keep on keeping on.
And I may well be reaching out to Dr. Kory depending upon the results I get from local docs.
I hope you are getting answers and relief. My blood tests finally came back - negative for Covid antibodies and nucleocapsid. So I doubt it was shedding. Rainwater test came back pretty good but my hair analysis indicates many heavy metals. Itchy rash continues.
I see you’re treating MCAS. Have you added the fibrinolytic enzymes to the protocol? I’ve seen it help in quite a few of our patients. I like Neprinol by Arthur Andrew Medical - it contrains, nattokinase, serrapeptase and bromelain.
Wondering if you have you seen the enzymes helpful in MCAS that isn’t related to Covid?
My young adult daughter has severe MCAS — along with EDS & POTS — that she’s had for most of her life. Would be great to have another option that might improve her control a bit more.
Hi Bluebird, I just joined this website looking for people who have skin issues. I see a lot of links to study in the replies, which I will start researching.
I am 62 and in good health generally. But I have had rashes for three years. I had mild eczema for several years before, pretty easy to treat, but noticed increasing issues with my skin as I was taking the three Moderna Covid doses in 2021 . The new rashes started in the armpit on one side (injection) but have now spread over much of my body. The rashes vary in character, and most are itchy. I have also lost a lot of hair. For a couple years I had pain in my axillary lymph nodes, but that seems to have gone away.
I just want to introduce myself with this post. I have only included one picture. Some of the rashes are hard to photograph without it feeling too private to put on the Internet.
I have consulted both regular MDs and two naturopaths who are my primary providers. I have tried many things, including the FLCCC protocols, leaky gut regimen, heavy metal detox, acupuncture, herbs, experimenting with diet and environmental triggers, etc I had a recent stem cell treatment which cleared up some of the rashing, but I still have problems. I think there is probably potential to still work on all of these same types of interventions, but I am frustrated that as careful as I am (organic, careful about blood sugar, moderate exercise, self care) I still have these skin problems three years on. It’s discouraging.
I’m looking forward to making some connections on this site.
Good luck, everybody!