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Re: Michigan CMT

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Bobbie

My Doctors are located in Farmington Hills. They are at the MIND CLINIC.

M Michigan

I Institute

N Neurology

D Disorders

It is located on Orchard Lake Rd near 12 Mile Rd. It is about 3 minutes from

expressway 696 and Orchard Lake Rd. This building was built and ran for nothing

else but neurology problems and my Doctor

Simpson and Dr. Rentz are awesome. They care and take their time. They

are 2 of 4 who run the MDA Clinic. Their staff is awesome. If you feel you

need something, they will write the prescription for your insurance company,

Medicare or Medicaid so you can get it. If you feel you need a scooter they will

write that also and help you get it. They will pay $2,000 maximum for it. They

can do their own testing there as well on another floor.

I really believe it would do you justice to make an appointment to see them. If

you think that you might like to give it a try call them at 1-734-416-7076 and

ask for . If she is not in leave a message, she is their right hand at the

clinic and you can talk to her and she will lead you in the right direction. I

wish you were closer than the 3-4 hour trip. We could get together. If you

decide you want an appointment, let me know and I will meet you

there and we can visit before or after. All appointments are in the afternoon

for adults starting at 12:30.

It would be worth the trip and I guarantee you won't regret it. This place is

awesome. Been dealing with them for 8 years now and my sister about 3 years

before that. You will have several people talk to you taking all kinds of notes

before the Dr. sees you. Please give it a shot. I know in my heart you won't

regret it.

I'd invite you to stay with me overnight, but am renting a room here in a

friends house and there are 3 very large dogs that can throw me off balance.

But if you make a day trip out of it or an overnight trip I love to get together

and talk.

Elaine

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  • 3 years later...
Guest guest

I have been reading messages from this site for about 13 years and have finally

decided to respond. I have CMT1A and it was confirmed 13 yeas ago. Never knew I

had CMT when I was younger.I also have three children who have CMT.

My daughter is 21 yrs old, one son who is 13 yrs., old and another who is 8yrs,

old. The 8 yr. old was a big surprise to our family and the fear that it would

be a 50% chance that he would have CMT. MY daughter has had 2 surgeries on her

left foot. One when she was 18 yrs. old and the other when she was 20 yrs old.

I'm sure she be going in for a 3rd surgery to fix the toes.

My 13 year old will be going in for his first surgery the summer of 2010 and the

other foot will be operated on during the summer of 2011.I live in Michigan and

for years could never find a doctor to help my daughter. Her foot was 2 1/2

sizes smaller than her right foot and it also toed in. We had to take her to

land for her first surgery and finally found a doctor in michigan to perform

the second surgery.

Luckly my husband works in the medical field and we were luckly to find this

doctor. It's been hard knowing three of our children were born with CMT and

will have to go through life with this disability.

I recently found out that I have relatives with CMT but have never met them.

They live in TN. I do have a cousin Tina who lives in Michigan and I noticed

this on the CMT site and would really like to know if were related.

CMT1A Michigan

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Guest guest

,

Are you asking me if i am your cousin Tina? i do live in michigan and i do have

cmt1a. i know all my 1st cousins, so i maybe a 2nd, and i do have family in tn.

From: heartpumper@...

Date: Mon, 3 Aug 2009 01:17:52 -0400

Subject: Re: Michigan CMT

I have been reading messages from this site for about 13 years and have finally

decided to respond. I have CMT1A and it was confirmed 13 yeas ago. Never knew I

had CMT when I was younger.I also have three children who have CMT.

My daughter is 21 yrs old, one son who is 13 yrs., old and another who is 8yrs,

old. The 8 yr. old was a big surprise to our family and the fear that it would

be a 50% chance that he would have CMT. MY daughter has had 2 surgeries on her

left foot. One when she was 18 yrs. old and the other when she was 20 yrs old.

I'm sure she be going in for a 3rd surgery to fix the toes.

My 13 year old will be going in for his first surgery the summer of 2010 and the

other foot will be operated on during the summer of 2011.I live in Michigan and

for years could never find a doctor to help my daughter. Her foot was 2 1/2

sizes smaller than her right foot and it also toed in. We had to take her to

land for her first surgery and finally found a doctor in michigan to perform

the second surgery.

Luckly my husband works in the medical field and we were luckly to find this

doctor. It's been hard knowing three of our children were born with CMT and will

have to go through life with this disability.

I recently found out that I have relatives with CMT but have never met them.

They live in TN. I do have a cousin Tina who lives in Michigan and I noticed

this on the CMT site and would really like to know if were related.

CMT1A Michigan

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Guest guest

Tina,

Yes, I was wondering if we were related. I have an aunt Dorothy who lives in TN

who has 5 boys. Also, I have an aunt Betty who lives in Warren,Mi who has 2

daughters, Debbie and Tina.

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Guest guest

george, no i am not related to them. thanks , but who knew, such a small world.

From: heartpumper@...

Date: Mon, 3 Aug 2009 16:53:04 -0400

Subject: Re: Michigan CMT

Tina,

Yes, I was wondering if we were related. I have an aunt Dorothy who lives in TN

who has 5 boys. Also, I have an aunt Betty who lives in Warren,Mi who has 2

daughters, Debbie and Tina.

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