hi chronic lyme patients, the one thing that causes me NOT to spend a lot of time on this very supportive, wonderful board is this fact. majority of us NEURO lyme patients can NOT read or comprehend LONG, solid blocks of text with NO PARAGRAPHS AND NO DOUBLE SPACING between each paragraph. when i come on here and see your long text block posts, i have just got to SCROLL ON BY, SOB, because my mind will not allow me to comprehend anything past the 1st 2-3 lines. i just can't do it. so i'd like to ask the members, especially those who post/reply alot, to think of the NEURO chronic lyme patients, and to please try to break up your posts every 2-3 sentences MAX unless you are a WORDY person, and 1 sentence would be 1 paragraph. i hope you understand what i'm saying and what i'm suggesting to you all. fyi, i've had chronic lyme 39 yrs; 34.5 yrs. MISDIAGNOSED BY 40-50 DRS. and my neuro is the pits! in my case, i never saw the tick nor did i have a bulls-eye rash, but using my daily journal tracked it back to my folks' LIVE XMAS TREE that it had to come off of. it was sub-zero iowa weather; roommates/i had NO PETS; i didn't garden and who could in sub-zero weather, and all the normal ways of getting ticks was eliminated. anyway, i thank you all for listening to what i had to say, and i'm not trying to pick on anyone; i just want to make you aware of more neuro lyme deficiencies we go thru too the longer we have this and UNTREATED as mine was for 34.5 years.  xox bettyg, iowa activist BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader
NOTE: I DO "NOT" USE CHAT thanks!
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NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)
http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-
Any information provided should not be used to take the place of advice from your personal physician or other professional.
Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.
43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
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"Mdjunction Tourette Syndrome site has given me the opportunity to share my experience of raising a child with TS, with others, especially those with new diagnosis. Support is essential for families and individuals with tourette as is information. I'm glad to have the opportunity to be there. I also learn as I go as others share their experience and knowledge." (Nevayda)
