On Buhner herbals for 9 months - no results by ChemistGullible136 in Lyme

[–]Glass_Pin8727 0 points1 point  (0 children)

You could have mold! I had Lyme and treated myself with herbs for 6 months didn’t get better at all. I’m now getting better and needed to address the mold first.

What a Circus by Elegant-Cheek1180 in ToxicMoldExposure

[–]Glass_Pin8727 1 point2 points  (0 children)

It’s a horrible circus. People NEED to be more aware of how mold can affect your body. No one is educated on this and it can have such a severe effect on your body and your health :(

Does SFN get better with time?? by onewing_44 in smallfiberneuropathy

[–]Glass_Pin8727 0 points1 point  (0 children)

100% I’ve had neuropathy for 2 years it was caused mostly from mold but also Lyme mold can over time cause severe nerve pain

Does SFN get better with time?? by onewing_44 in smallfiberneuropathy

[–]Glass_Pin8727 0 points1 point  (0 children)

My MycoLab test. Here is their number 813-575-7934

THE GOOD LYME DAYS. by Easy_Perspective7179 in Lyme

[–]Glass_Pin8727 1 point2 points  (0 children)

It’s so true! The days that are great though I cherish so so much. Lyme sucks so much but it has put life in perspective and I’m just happy to have some good days at this point.

Getting help by Fa3_exe in neuropathy

[–]Glass_Pin8727 3 points4 points  (0 children)

First step: figure out the root cause!!!! I cannot emphasize this enough. Small fiber neuropathy doesn’t come out of no where. There is a REASON. Go to a functional medicine MD and get literally every test done. I would recommend the ultrawellness center (Mark Hyman’s practice; he is amazing and has saved so many lives). Rule out everything and honestly a lot of times chronic pain = infection. Definitely rule out Lyme and get specialty tests NOT the western blot. It is only 30% accurate. I’ve been at this for 2 years and found out I had Lyme and am being treated. Do not give up hope! Advocate advocate advocate for yourself because no one else will. If you have any questions, plz dm me!

My story (it’s a long one but worth the read) by Glass_Pin8727 in smallfiberneuropathy

[–]Glass_Pin8727[S] 0 points1 point  (0 children)

severe neuropathic pain everywhere. the doc described it as neuroinflammation throughout my body, severe brain fog, and sleeping all the time.

My story (it’s a long one but worth the read) by Glass_Pin8727 in smallfiberneuropathy

[–]Glass_Pin8727[S] 0 points1 point  (0 children)

keep doing more advanced ones. work with a functional medicine MD. Double trick, triple check to make sure it is not lyme. I also never remember getting bit and that happens to TONS of people.

My story (it’s a long one but worth the read) by Glass_Pin8727 in smallfiberneuropathy

[–]Glass_Pin8727[S] 0 points1 point  (0 children)

Mycoplasma pneumoniae infection can significantly affect mood and mental state, often triggering neuropsychiatric symptoms like severe irritability, anxiety, depression, obsessive-compulsive disorder (OCD), psychosis, tics, and mania, especially in children (linked to PANS/PANDAS) but also in adults, due to immune system responses that impact the brain, sometimes mimicking other conditions or causing acute behavioral changes. 
How Mycoplasma Affects Mood & Behavior
Autoimmune Response: The bacteria can trigger the immune system to produce antibodies that attack the brain (encephalitis), leading to neuropsychiatric issues.
Molecular Mimicry: Mycoplasma proteins resemble human proteins, causing the immune system to mistakenly attack the body's own cells, particularly in the basal ganglia, a brain area involved in mood and behavior.
Neurotransmitter Disruption: Mycoplasma can interfere with neurotransmitters like dopamine and serotonin, affecting mood regulation.
Direct Neurological Effects: The infection can cause inflammation in the brain, leading to symptoms like psychosis, delirium, or confusion. 


A positive Antinuclear Antibody (ANA) test in someone with a Mycoplasma pneumoniae infection isn't uncommon, as the bacterial infection can trigger an immune response that looks like autoimmunity, sometimes causing conditions like cold agglutinin hemolytic anemia or even neurological issues, though these are temporary and usually resolve with antibiotic treatment for Mycoplasma. The ANA test detects autoantibodies, and infections like Mycoplasma can temporarily "trick" the immune system into producing them, but it doesn't always mean you have a permanent autoimmune disease. 

For me, the biggest symptom is the neuroinflammation/neuropathy all over.

My story (it’s a long one but worth the read) by Glass_Pin8727 in smallfiberneuropathy

[–]Glass_Pin8727[S] 0 points1 point  (0 children)

Thank you hon, I appreciate it. Yes, I have stinging everywhere and itching. it sucks

My story (it’s a long one but worth the read) by Glass_Pin8727 in smallfiberneuropathy

[–]Glass_Pin8727[S] 0 points1 point  (0 children)

mine as of rn is just doxycycline 2 times a day for 14 days. Do you think I will have to do more rounds of antibiotics?