Help: petichiae

Posted by lidiana @lidiana, Nov 5, 2022

Hi 👋🏻

I have been really sick and I just wanted to know how many of diagnosed people had this symptoms:

✅petichiae (the new spot appeared on my nose)
✅ severe bone pain
✅ leukoplakia on gums
✅ bloating
✅ nausea
✅ severe abdominal pain
✅ low urine or retention
✅ constipation or extreme diarrhea
✅ breathing difficulties
✅ heart rate abnormalities
✅ movement impairment
✅ syncope
✅ hemorrhagic gastritis
✅ spot on bladder with hyper vascular inflammatory changes according to biopsy
✅cyst on brain, neura foramina, ovaries, liver, kidney and “intramural fibroid” (confirmed on pet scan and MRE)
✅ patchy lesions on bone scans
✅ constant high D DIMERs
✅ high tumor markers CA 19.9 Chromogranin A
✅ High cardiolipin
✅ positive and negative ANA test
✅ speech impairment
✅ new massive headaches

I’m scared for my life and health at this point. I have begged for biopsies…😓

Any feedback would be greatly appreciated 🙏🏻 Blessings and healing 🌼

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Have you seen a metobolic doctor? I have petecia all over my trunk, bone pain, cysts on different organs, frontal lobe lesions, nonketonic hyperglycemia, CNS orthostatic hypertension, and a few more new diagnoses that I am waiting for my metobolic doctor to go over, as well as out of control lab work. If you have raw data from 23 & me you can upload it to genetic genie to get a better idea of some of your markers which in turn will help your doctors know where to look. I recommend getting tested for the MTHFR gene mutation because it is linked to cancer due to detoxification issues and demyelination and methylation problem.

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by lidiana @lidiana, it's sounds like unsolved medical mysteries (glad your trying to keep a record of symptoms (what's what's) Feel better soon. Good doctors help; but they are rare as the disease. How are your doctors and specialists? What about support family/friends / groups or do you feel alone? How are you dealing with this?

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@raremiracle2

by lidiana @lidiana, it's sounds like unsolved medical mysteries (glad your trying to keep a record of symptoms (what's what's) Feel better soon. Good doctors help; but they are rare as the disease. How are your doctors and specialists? What about support family/friends / groups or do you feel alone? How are you dealing with this?

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@raremiracle2 i think I’ll be getting a good lawyer lol but yeah I have my support groups and loved ones. Most importantly my God that’s sees everything and I trust his righteous hands 🙌🏻🙏🏻👁️

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lidiana | @lidiana I agree the most importantly our God that’s sees everything and I trust his righteous hands. Most power and your voice makes the difference. Keep your faith and hanging in there! We are with you! Keep us updated!

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@chefdecemberskye i do have MTHFR mutation and TNXB. I’m being followed up with oncologist OBGYN and I’m trying to get colorectal surgeon plus a gastroenterologist oncologist but that’s very hard at Kissimmee…

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Also I have foci T2 spots on brain and new one is 3mm and positive Ana test with mitotic spendle fibers… still being dismissed 😞

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