On the positive side , you figured it after the first gd injection , unlike sadly others that have had multiple injections before connecting the dots . 😢. And you are being an advocate and alerting others of the dangers . Thanks Kate .
You are on the right track identifying that the root cause of your symptoms is your immune system that was triggered by gd. I had a bad reaction to gd and I had underlying autoimmune disorders prior to the injection like atopic dermatitis , allergies and hashimoto . The mast cell activation syndrome makes a lot of sense
Whenever i get a scan with gad i take chelators for it. Cilantro, other things, things for kidney and liver like NAC, etc Also, the burning etc can be from MRI being operated wrongly. Also, i might have an undiagnosed fatty acid oxidation disorder... Its being checked out now.... Or an amino acid disordrr .. i have high sarcosine, high hydroxylysine, low histidine
This is so crazy, I totally have the impending doom episodes, and also have osteoarthritis/bone spurs in my spine which is crazy as a 23 year old. I’ve also ALWAYS had asthma and allergies, rhinitis, chronic sinusitis, etc. The headache feeling like it’s pushing against my head too. And the DISSOCIATION, big time. Holy moly. Gonna try and see an allergist/immunologist.
WOW! It's insane. Try to find a specialist who understands mast cell activation syndrome because, unfortunately, many allergists don't. It's newer information & science
@@bondswithoutbounds Ok will do. I live in NY so I’m gonna try reaching out to the one in the video you linked to. I’ve also been watching her other stuff. It sort of seems like maybe those of us who were immunocompromised to begin with might have been more susceptible to Gad? Have we ever done a surgery to see how many people with GDD have, like, asthma, allergies, MCAS, or other autoimmune stuff?
@@firstnamelastname159 Oh wow, I have no idea who you are because of your anonymous name but please let me know if you meet with that doctor & what she says! If you’re able to make any progress or discover anything new, I definitely want to hear back so we can figure out more pieces to the puzzle🤍🧩
I've not noticed much of a difference between turmeric curcumin supplements. I need to find the bottle for the PEA & I will let you know when I find the brand name!
@@bondswithoutbounds In this video you mentioned you watched another video of a woman bringing awareness about mast cells and not to get MRI contrast and you said you were going to link it in this video?
You have to think long term, in 10 years or less, you can definetly recover from gad toxicity and have your life back. Keep moving/ walking, fast during the day, drink MM heavy metal detox smoothies, eat meat at night. Organs, bone, brain all heal themselves but it does take a long time.
@@xhealmeplease The brain heals so long as it doesn’t keep losing oxygen or getting attacked by the immune system that tries to kill gad! What would change at the 10 year mark?
@@bondswithoutbounds imagine 10 years into the future of being active vs 10 years without. Its unfortunate that were suffering from this disease, but it happened. I walk every day at minimum, just to keep my blood flowing, theres some chleting properties to that, should aid in removing gad from bone, and once its in muscle tissue its able to sweat out. The choice is let this disease bring you down, or push every day for a brighter future.
@@bondswithoutbounds sorry to hear that. During my initial week after the contrast dye, it felt like my legs were going to snap everytime i took a step. I just kept walking, being careful of how i aligned my knee/legs every time i took a step foward. Eventually it got better overtime, but im nowhere near how i was before the injection. I feel like it stored itself in my connecting joint or bone and is releasing slowly. I dont think the solution is to use a drug like dtpa to remove the gadolinium since it removes the gadolinium fast and could cause horrible side effects, but its to find a drug that strengthens the flesh. Low dose steroids might help until youre able to walk without them.
Thank you for sharing your story. I didn’t know about this until I saw your channel today and I already told my mom. I’m gonna tell everyone I know.
On the positive side , you figured it after the first gd injection , unlike sadly others that have had multiple injections before connecting the dots . 😢. And you are being an advocate and alerting others of the dangers . Thanks Kate .
You are on the right track identifying that the root cause of your symptoms is your immune system that was triggered by gd. I had a bad reaction to gd and I had underlying autoimmune disorders prior to the injection like atopic dermatitis , allergies and hashimoto . The mast cell activation syndrome makes a lot of sense
Omg this is so so helpful I’m definitely gonna try these things out.
Whenever i get a scan with gad i take chelators for it. Cilantro, other things, things for kidney and liver like NAC, etc
Also, the burning etc can be from MRI being operated wrongly.
Also, i might have an undiagnosed fatty acid oxidation disorder... Its being checked out now.... Or an amino acid disordrr .. i have high sarcosine, high hydroxylysine, low histidine
This is so crazy, I totally have the impending doom episodes, and also have osteoarthritis/bone spurs in my spine which is crazy as a 23 year old. I’ve also ALWAYS had asthma and allergies, rhinitis, chronic sinusitis, etc. The headache feeling like it’s pushing against my head too. And the DISSOCIATION, big time. Holy moly. Gonna try and see an allergist/immunologist.
WOW! It's insane. Try to find a specialist who understands mast cell activation syndrome because, unfortunately, many allergists don't. It's newer information & science
@@bondswithoutbounds Ok will do. I live in NY so I’m gonna try reaching out to the one in the video you linked to. I’ve also been watching her other stuff. It sort of seems like maybe those of us who were immunocompromised to begin with might have been more susceptible to Gad? Have we ever done a surgery to see how many people with GDD have, like, asthma, allergies, MCAS, or other autoimmune stuff?
@@firstnamelastname159 Oh wow, I have no idea who you are because of your anonymous name but please let me know if you meet with that doctor & what she says! If you’re able to make any progress or discover anything new, I definitely want to hear back so we can figure out more pieces to the puzzle🤍🧩
Thank you for sharing.
Did you really had a stroke as the result of gadolinium or some type of nerve dysfunction?
maybe thats why hbot helps some people really much
Which PEA and Curcumin supplements do u recommend?
I've not noticed much of a difference between turmeric curcumin supplements. I need to find the bottle for the PEA & I will let you know when I find the brand name!
@@bondswithoutboundsthat would be awesome thanks!
Where is the link for the video, about mast cells and the warning to not get gadolinium contrast?
@@katrinaolson673 This is that video
@@bondswithoutbounds In this video you mentioned you watched another video of a woman bringing awareness about mast cells and not to get MRI contrast and you said you were going to link it in this video?
Love you
@@melissaborkin1922 Love you more!!
You have to think long term, in 10 years or less, you can definetly recover from gad toxicity and have your life back. Keep moving/ walking, fast during the day, drink MM heavy metal detox smoothies, eat meat at night. Organs, bone, brain all heal themselves but it does take a long time.
@@xhealmeplease The brain heals so long as it doesn’t keep losing oxygen or getting attacked by the immune system that tries to kill gad! What would change at the 10 year mark?
@@bondswithoutbounds imagine 10 years into the future of being active vs 10 years without. Its unfortunate that were suffering from this disease, but it happened. I walk every day at minimum, just to keep my blood flowing, theres some chleting properties to that, should aid in removing gad from bone, and once its in muscle tissue its able to sweat out. The choice is let this disease bring you down, or push every day for a brighter future.
@@xhealmeplease And what is the solution for those who cannot walk because of gadolinium toxicity?
@@bondswithoutbounds sorry to hear that. During my initial week after the contrast dye, it felt like my legs were going to snap everytime i took a step. I just kept walking, being careful of how i aligned my knee/legs every time i took a step foward. Eventually it got better overtime, but im nowhere near how i was before the injection. I feel like it stored itself in my connecting joint or bone and is releasing slowly. I dont think the solution is to use a drug like dtpa to remove the gadolinium since it removes the gadolinium fast and could cause horrible side effects, but its to find a drug that strengthens the flesh. Low dose steroids might help until youre able to walk without them.