Re: Multiple Sclerosis/MS
In reverse order:
My sister has Lyme Disease. The spirochete has been found in her csf. She may have other things as well, I do not know. We have some overlap in symptomology but I'm willing to accept her malady is a result of at least one contact with a deer tick.
Our adoption was through an agency in San Diego and I have the papers (including original letters of recommendation etc) so I know who to contact. I have no illusions or fantasies. I was physically abused as an infant (nearly to death) and it took me a long time to recover. I've had lingering health outcomes because of this, and a number of psychological hurdles to overcome as well. There is no secret wish to meet. Maybe if someone wanted to tell me the truth abou the story...but other than strictly for informational purposes. The only other information I am interested in is the nationality (ie. northern european or whatever). That's it.
I'm sorry to all who feel otherwise, but the idea of getting emotional about people i've never known has never made much sense to me. Perhaps if they hadn't come so close to killing me, I'd feel otherwise. Who knows. Even if the other party wanted to meet, I would be deeply hesitant. There is no emotional attachment, nor do I wish one.
But you have given me a direction to go, and I have the appropriate information to pursue this line.
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Re: Multiple Sclerosis/MS
Thank you for your wonderfully informative post.. I am currently trying to get a diagnosis for what i believe is Andersen Tawil syndrome,, It is an ion channelopathy that i believe comes down my french canadian lines,, I am not a geneologist and have only had luck tracing my mothers fathers line back to some of the early settlers in new canada,, My grandmothers paternal line is also all french canadian back to the early centuries,, both of these lines cross with zacharie cloutier and xainte duponts lines many many times over the generations,,I am soon to send my blood and my sons blood to Dr. lehman horne at the university of ulm in Germany for genetic testing,,depending on what he finds more family members will be sending their blood also.this condition is considered to be a type of muscular dystrophy with many similarities to opmd. my identified french ancestry names are dube and levasseur,,
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Re: MS IN MULLINS/MULLIS FAMILIES
Mullis family descending into Orange Co., N. C. in 1755 were descended from John Mullis who arrived in Va. by June 8, 1658, an ENGLISH IMMIGRANT FROM MICHAELSTOW PARISH, CORNWALL.
THIS MULLIS FAMILY HAD NO CONNECTION WHATSOEVER TO SWITZERLAND, where a separate Mullis surname evolved from the name of village near Flums called Mollis.
Important to keep English Mullis lines separate from Swiss Mullis lines, especially when studying genomes.
Arthur Mullies
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Re: Multiple Sclerosis/MS
family here struggling to identify SCA , all athena tests negative, fyi, University of Michigan currently conducting ataxia research for anyone still trying to get their SCA's identified.
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Re: Multiple Sclerosis/MS
ask for non identfing info on you adoption.It might give you a clue to find more a.bout the famiilyIf you were adopt from the state of california your parent will have her name on the papers. I saw my papers but my birth mother died when Iwas 6 in 1937 of TB.
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Re: Multiple Sclerosis/MS
ask for non identfing info on you adoption.It might give you a clue to find more a.bout the famiilyIf you were adopt from the state of california your parent will have her name on the papers. I saw my papers but my birth mother died when Iwas 6 in 1937 of TB.
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