Platypus wrote:Why does your friend need to go so far for a new doctor? If she's already been diagnosed and prescribed medication, can't she just see a local doctor to have the prescriptions refilled as necessary?
Is there a school counsellor she can talk to for support?
The issue with CLD is that insurance companies do not usually cover the long term treatment because there is controversy to whether the Lyme bacteria stays in the body that long.. There are no local doctors that are willing to prescribe the powerful medications that kill the Lyme bacteria to her because they fear that the Lyme bacteria will develop a resistance to the medication. Although that is possible it's better than having the disease progress. So now she has to find doctors out of state which can be very expensive. This is what lyme disease dot org says about chronic lyme disease.
If Lyme disease is not diagnosed and treated early, the Lyme spirochetes can spread and may go into hiding in your body. Weeks, months or even years later you may have problems with your brain and nervous system, muscles and joints, heart and circulation, digestion, reproductive system, and skin. Symptoms may disappear even without treatment and different symptoms may appear at different times.
and here's a graph showing the most common neurological symptoms
http://lymedisease.org/lyme101/lyme_dis ... ptoms.htmlI just don't know what to do at this point.