Thank you. Along with “Bitten” which I read as soon as it was published, your comments help this person who has had Chronic Lyme for 39 years. Same old same old made up stories about that.
Growing up in the woods surrounding the Fish Hatcheries my Father ran in Idaho in late 40’s and early to mid-50’s my family was well aware of wood ticks. I thought my Father such a hero when he took them off us We never became sick.
It was 1985 and hiking in Prince William Forrest Va. one day before I worked a Pan Am flight the next day to Frankfurt Germany . While relaxing in the tub in my hotel I noticed what I mistook for a new mole on my abdomen . I slid my finger over it and lo’ and behold, legs moved. This tick was the size of a sesame seed. I was grown up, brave now and my Father was in Idaho…. I burned the tick in the sink( yes, hotels still had candles and matches in the rooms).
During the next year I moved from Va. to San Fran. Ca. During that year little, bizarre issues came up physically. I had various treatments for flu like pains in joints, flu like many times. Until in 1987 I could not get up from my bed. Called Pan Am and said” I think I am dying”. It took two years and an article in a medical journal written by a nurse practitioner writing about having experienced a bolt of lightning flashing through her brain. That had happened to me while driving to work the 6 months prior. She had Lyme disease. That bolted and jolted my memory and I told my doctor, Dr.Jeffry Anderson who was in Corte Madera that I had Lyme disease.
He had been treating me for CFIDs, chronic fatigue immune deficiency.
I then began a very long journey ….. treatments from Ca.to Ny, to Ct.,to Va.
I am now going to a very fine clinic in Mexico. I am 78 years old. Waiting waiting for our government to tell the truth, or for insurance corporations to tell the truth, or for doctors across America to gain some factual knowledge and not blame the patience.
Thank you for bringing “Bitten” out of moth balls…..where the crooks want it kept.
Can you please share the name of the clinic, how long do you need to stay there?, more help for us still suffering after numerous treatment regimens. Thanks.
I was seen in 2023 by a Stanford neurologist and brought up history of Erythema Migrans rash and tick bites. I suspect that I have neurologic Lyme instead of Multiple Sclerosis, a diagnosis I was given in 2000. I pointed out that because Lyme leaves the bloodstream quickly, a Lyme test probably would come back negative, and that the CDC explains that testing is for surveillance only, and a Lyme is clinical diagnosis.
I asked for referral to infectious disease, and this was the response,
"Please note that Dr.... has placed a Stanford ID referral per your request, and we were informed that they do not accept our referral because the Stanford ID clinic has a long-standing policy of NOT seeing patients for Lyme Disease or "Tick Bite" if Lyme is the concern." !!!!???? What is that about if not denial and gaslighting? Unbelievable.
Re-reading “Bitten” now. A family member recently found embedded, engorged ticks in our high Lyme disease area of New England. It seems the two options are to do nothing until symptoms appear. Or take doxycycline as a precaution. Neither are good choices.
Thank you. Along with “Bitten” which I read as soon as it was published, your comments help this person who has had Chronic Lyme for 39 years. Same old same old made up stories about that.
Growing up in the woods surrounding the Fish Hatcheries my Father ran in Idaho in late 40’s and early to mid-50’s my family was well aware of wood ticks. I thought my Father such a hero when he took them off us We never became sick.
It was 1985 and hiking in Prince William Forrest Va. one day before I worked a Pan Am flight the next day to Frankfurt Germany . While relaxing in the tub in my hotel I noticed what I mistook for a new mole on my abdomen . I slid my finger over it and lo’ and behold, legs moved. This tick was the size of a sesame seed. I was grown up, brave now and my Father was in Idaho…. I burned the tick in the sink( yes, hotels still had candles and matches in the rooms).
During the next year I moved from Va. to San Fran. Ca. During that year little, bizarre issues came up physically. I had various treatments for flu like pains in joints, flu like many times. Until in 1987 I could not get up from my bed. Called Pan Am and said” I think I am dying”. It took two years and an article in a medical journal written by a nurse practitioner writing about having experienced a bolt of lightning flashing through her brain. That had happened to me while driving to work the 6 months prior. She had Lyme disease. That bolted and jolted my memory and I told my doctor, Dr.Jeffry Anderson who was in Corte Madera that I had Lyme disease.
He had been treating me for CFIDs, chronic fatigue immune deficiency.
I then began a very long journey ….. treatments from Ca.to Ny, to Ct.,to Va.
I am now going to a very fine clinic in Mexico. I am 78 years old. Waiting waiting for our government to tell the truth, or for insurance corporations to tell the truth, or for doctors across America to gain some factual knowledge and not blame the patience.
Thank you for bringing “Bitten” out of moth balls…..where the crooks want it kept.
Sincerely,
Can you please share the name of the clinic, how long do you need to stay there?, more help for us still suffering after numerous treatment regimens. Thanks.
Bioadvanced medical clinic. Dr.Calzada .
Tijuana , Mexico
Immaculate clinic with Doctors trained at Oxford, Germany, Mexico City.
Hotel Lucerna gives a special rate through clinic. Excellent. Like a vacation only one feels finally well!
Can you give a phone # or email for contact info??? Great thanks!!!!
Tel. USA(619)754.48.85
www.bioadvancedmc.com
Jane,
I will send you info tomorrow . Late now and I have an early day.
Thank you for inquiring.
Can you do anything to educate your colleagues at Stanford? They misdiagnosed me, said I should be aware of Post-Polio Syndrome‼️
After 50+ years of gaslighting by the medical community a Naturopath figured my symptoms out in 2 hours 🤯
I was seen in 2023 by a Stanford neurologist and brought up history of Erythema Migrans rash and tick bites. I suspect that I have neurologic Lyme instead of Multiple Sclerosis, a diagnosis I was given in 2000. I pointed out that because Lyme leaves the bloodstream quickly, a Lyme test probably would come back negative, and that the CDC explains that testing is for surveillance only, and a Lyme is clinical diagnosis.
I asked for referral to infectious disease, and this was the response,
"Please note that Dr.... has placed a Stanford ID referral per your request, and we were informed that they do not accept our referral because the Stanford ID clinic has a long-standing policy of NOT seeing patients for Lyme Disease or "Tick Bite" if Lyme is the concern." !!!!???? What is that about if not denial and gaslighting? Unbelievable.
Re-reading “Bitten” now. A family member recently found embedded, engorged ticks in our high Lyme disease area of New England. It seems the two options are to do nothing until symptoms appear. Or take doxycycline as a precaution. Neither are good choices.