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NIH/All members of CEDA

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Cindy~~

I could not afford to go to land but am certainly up for a phone call.

I have III and was diagnosed by my Rheumatologist 2 years ago after about 20

orthopedic/ mostly reconstructive surgeries and countless injuries all my

life.

You can get me off list and I will send my phone number.

NIH/All members of CEDA

hEY ALL, I'm hVING TROUBLE with this PC, it's nothing like

mine,Anyway, DR F. and Dr Naz asked me to put this up to our list.

Apparently they didn't know this study was not on the NIH list for

all to find. They guess that is because it is at the Bayview Hospital

instead, something like that. Anyway, they asked me to put this on

the list for all. They want people. All types EDS even if they don't

have a definate DX from a Genetics DR. They will interview you on the

phone if you don't have a DX. (Dang PC) When I get home late tomorrow

PM I will give all the info. They want you to caLL. i AM ALREADY

AMAZED ABOUT THINGS WE HAVE FOUND OUT HERE ABOUT dYLAN. To much to

even try to explain this late at night. We have more answers in 24

hours than we have had in over a year. My heAD IS SPINNING. ( dang

PC!) I want my own bed and computer. Whaaa. No really, this is just

great. My gut told me this is where we needed to be. Just bring your

own pillows!!!! On Thursday look for the info if you can travel to

land. Today, Jen in Ariz got in, Lana got in, S got in, and

Dr F looked at Meagans (Canada) Papers and looked at me and said I'll

see what I can do. But Meagan, the papers I had, didn't have your

home info on it. Just Dr Grubbs. I'll have you contact Dr f when I

get home. She is very interested in helping however she can.

I'll write later on what we have found ABOUT dYLAN. all is so much

more involved than what we knew. My head is spinning. Seems things

are much worse than we thought. Tomorrows test should help put things

together a BIT CLEARER. tHE dOCS ARE WAiTING FOR TESTS DONE NEAR

HOME, from last year, TO ARRIVE HERE IN THE am TO DO COMPArisims to

make a determination on what is happening to him. ( I do not like

this key board, or it does not like me). I'll write more tomorrow.

Night aLL. tHIS PLAce is amazing.

Cindylouwho

To learn more about EDS, visit our website: http://www.ehlersdanlos.ca

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Grace, The info is below, give them a call or email or both. If you want to talk

on the phone, just email me at home and we can exchange numbers.

c-clark05@...

Cindylouwho

Nazli McDonnell M.D. Ph.D.

Clinical Fellow

NIA/NHGRI

mcdonnellna@...

ph (TRIAD):

ph(Harbor-ASTRA):

NIH/All members of CEDA

My 2 boys and I would LOVE to be in on this study as well. Email me and I'll

give you my phone number too!!!!! I would love to have some answers.

HUGGLES,

Grace

EDS, It's a Life Thing

http://www.ehlersdanlos.ca/whateds.htm

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Grace, The info is below, give them a call or email or both. If you want to talk

on the phone, just email me at home and we can exchange numbers.

c-clark05@...

Cindylouwho

Nazli McDonnell M.D. Ph.D.

Clinical Fellow

NIA/NHGRI

mcdonnellna@...

ph (TRIAD):

ph(Harbor-ASTRA):

NIH/All members of CEDA

My 2 boys and I would LOVE to be in on this study as well. Email me and I'll

give you my phone number too!!!!! I would love to have some answers.

HUGGLES,

Grace

EDS, It's a Life Thing

http://www.ehlersdanlos.ca/whateds.htm

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Hi Debbi, I don't know exactly how that would work to talk to them for help. I

do know they accept phone calls from Drs looking for answers for their patients.

If your Doc had specific questions for them as how to treat you, I know they

will talk to him/her. I suppose it wouldn't hurt to email some questions and see

what happens. Sorry I can't be more help.

Cindylouwho

RE: NIH/All members of CEDA

Cindy~~

I could not afford to go to land but am certainly up for a phone call.

I have III and was diagnosed by my Rheumatologist 2 years ago after about 20

orthopedic/ mostly reconstructive surgeries and countless injuries all my

life.

You can get me off list and I will send my phone number.

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