posted
I am scheduled for my first medical exam for Saturday, can anyone tell me what to expect?? and maybe give me some advice??? I sure would appreciate it. Thanks, Sandie
Posts: 45 | From michigan | Registered: Jun 2008
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Ocean
Frequent Contributor (1K+ posts)
Member # 3496
posted
Sandie, I don't have any experience or suggestions, but just wanted to say good luck. Keep us posted!
posted
Feelfit & Lisas,Thanks for your reply, The Dr. was nice to a point, she had a waiting room full of patients and was the only Dr. there on a Saturday, so I took that into consideration B/C she was kinda impatient.
She asked me a lot of questions about my Lyme and my history before my Lyme diagnosis,she had me bend and touch my toes,hop on one foot, just basic things. She believes that I HAD lyme, but after her exam and hearing my history, she believes I have MS, she said after being on ABXS, the lyme would be gone! So, I let her talk and did not argue with her, boy was that hard.
She said I have nerve damage down my right side, I thought to myself, gee thats a surprise, I've known that for 10 years.
I legitimately failed her neurological test, she said I was very weak and that she believed I was truly sick and that she would do what she could do to get me approved.
I feel encouraged by her statement to me, but know its in the hands of SSDI to decide, So I expect to get a denial, then I can start the appeals process. Well.... you never know,maybe I'll get approved the first time, Wouldn't that be nice. Take care all, Sandie
Posts: 45 | From michigan | Registered: Jun 2008
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bettyg
Unregistered
posted
sandie,
thanks for update on your visit, and glad she did agree on some things!
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Your welcome BettyG , Thank you for always being so kind. Take care, Sandie
[ 08. December 2008, 04:48 PM: Message edited by: sandiet ]
Posts: 45 | From michigan | Registered: Jun 2008
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LisaS
Frequent Contributor (1K+ posts)
Member # 10581
posted
SAndiet, It's frustrating when we know more than our Drs about lyme huh? Well I hope she does fight for you and you do get it! I'll put you in my prayers!!!!
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Thanks Lisa, I need all the prayers I can get.
Yes, it is frustrating to think we know more about a disease then our mainstream Doc's know.
Hopefully, someday they will know the truth!!
Take care, Sandie
Posts: 45 | From michigan | Registered: Jun 2008
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lymednva
Frequent Contributor (1K+ posts)
Member # 9098
posted
Sandy,
It sounds like you got what you needed from that doctor. It's not the dx that counts, but the fact that she noted you had neuro problems and weaknesses.
You will have a better chance of being approved. That is the goal, no matter what they call it.
-------------------- Lymednva Posts: 2407 | From over the river and through the woods | Registered: Apr 2006
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