Roxy, je schrijft:
...In de praktijk blijkt dat sommige Ilads Lyme&me/cvs artsen uit Nederland en het buitenland veel roepen...
Okee,
Om te beginnen kun je borreliose niet in 1 mond met ME neerzetten, omdat borreliose ten eerste een infectieziekte is veroorzaakt door een bacterie, en ME is dat niet.
Ten tweede niet omdat ME een erkende ziekte is en chronische borreliose niet.
...maar voor het gestelde geen medische en wetenschappelijke onderbouwing geven....
Verder over dat maar een beetje roepen van de ILADS artsen, is geen zomaar roepen, het is gebaseerd op jarenlange onderzoeken - ook wetenschappelijk - lees desnoods eens de referenties
Voor het gemak zal ik ze voor je hier plaatsen:
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....Ook zijn de artsen wispelturig bij de gebruikte testen bij de diagnosestelling. De ene keer wordt er een LTT test aangeraden (en wordt de 'betere/beste' test genoemd) van laboratoria in het buitenland. ...
Zo zwart/wit is het niet.
Wanneer je ooit eens zelf onder behandeling bent geweest v.e. ILADS werkende arts, zul je gaan begrijpen hoe het zit met bv het gebruik van antibioticum, de duur van je ziekte, de wel of niet aanwezige co infecties, o.a. en de invloed van ALLE testen hierop
Het ligt echt anders dan je hier zo kort door de bocht stelt
....En de andere keer is men weer overgestapt op zogenoemde 'nieuwe' testen die bij nadere bestudering experimentele of niet-gevalideerde testen ('Phelix Phage Borrelia test', 'Fish test'....
De fagen test kan ik niets over zeggen, want heb deze nooit gebruikt, maar de FISH is al veel langer in omloop ook voor borrelia, [ lees bv eens het oude lymeNet]
...'Phelix Phage Borrelia test' dat zelfs werd gepromoot in Nederland bij de ZonMw - Werksessie ME/CVS 4 november 2020 Utrecht...
Dat ZonMw zoiets promoot voor ME vind ik heel erg.
Men zou beter een onderzoek kunnen gaan starten voor de oorzaak van ME, want dat is nog steeds onbekend.
Begrijpelijk dat veel mensen met ME daar gehoor aan gaven, wel erg triest.
...Ook worden er afwisselend zogenoemde 'nieuwe' behandelingen voorgesteld en voorgeschreven. Bij nadere bestudering blijken dat regelmatig experimentele, kostbare (€10.000 - €20.000 (per jaar)), langdurige en niet-medische en niet-wetenschappelijke onderbouwde behandelingen te zijn....
Ik weet niet of je hier spreekt over ME of over borreliose
Maar in mijn geval [ borreliose ] heeft het bij lange na niet deze enorme bedragen gegeven.
Bovendien handelde mijn arts volgens de bekende literatuur.
Het enige wat zo duur kan zijn is wanneer je eoa uitgebreide kruiden therapie volgt, ik kan het me anders niet voorstellen dat het zoveel zou moeten kosten, antbioticum is in de regel heel goedkoop.
IV cef is wel duur, maar heeft geen zin voor Bartonella.
En bij een co infectie met bart heeft een iv behandeling ook niet veel zin.
Het is prettig wanner je zelf ook inleest en meedenkt ( als patient zijnde)
Ik vind het erg dat sommige ME patienten denken de ziekte van lyme te hebben
Het zijn twee totaal verschillende ziektes.