In the midst of all the celebration of my mother and step-father's 50th anniversary we discover a family member(neither of us), is diagnosed with AND suffering very much from Lyme disease to the point of being unable to travel 8 miles to be part of an event months in the planning.
We are looking for non-generic Lyme disease information, that is, for information and resources proven useful for someone you know, if not yourself. The victim is male, in his early fifties, generally an active and rugged out-door type with wide ranging interests... who is recently reduced to "hurting in places he didn't know he had" ... as his son reports it.
Generic information or resources localized for Maryland or the Mid-Atlantic might help as well.
We're on the road, have had a very mixed connectivity weekend, and may not be able to check in again until Tuesday or even Wednesday.
TIA!
Steve
We are looking for non-generic Lyme disease information, that is, for information and resources proven useful for someone you know, if not yourself. The victim is male, in his early fifties, generally an active and rugged out-door type with wide ranging interests... who is recently reduced to "hurting in places he didn't know he had" ... as his son reports it.
Generic information or resources localized for Maryland or the Mid-Atlantic might help as well.
We're on the road, have had a very mixed connectivity weekend, and may not be able to check in again until Tuesday or even Wednesday.
TIA!
Steve
Re: IDSA, undertreats
2008-07-21 18:09 (UTC)My inclination would be to treat the IDSA guidelines as a minimum level of treatment; if your family member is still having Lyme-related symptoms and/or difficulties, perhaps more agressive treatment is warranted. Although I am somewhat concerned that ILADS guidelines are inclined more towards over-diagnosis and over-treatment, in the absence of conclusive data one way or the other, which set of guidelines to follow must be left to the judgement of the individual patient and practitioner.