Hi Dennis
I think I remember your name from a few years ago when tmic was a much
busier web site. I was tested for West Nile Virus when I was diagnosed
with TM, however, I am one of those with no idea how or why I developed
it.
I'm fortunate to be able to walk with a cane and returned home
I had the same neurologist for first five years of TM. I had several
MRI's and he was satisfied that I didn't have MS (TM left me with
cognitive problems). I had been on the same medications for two years,
my primary said he would renew my rx when needed, and I didn't feel the
need to
I've noticed some talk of people comng back to the tmic list for
discussions and wondered just how many people actually look at this site
anymore. The onky discussion I have is that I received my first flu
shot last Wednesday since my 9 years with TM. We had two deaths from
the flu in our
Thank you for sharing and for all the hard work that went into this
event. We will all benefit from your efforts since ythe money is going
to TM research.
Patti - Michigan
On Thu, Apr 12, 2012 at 1:41 PM, Deborah Nord Capen wrote:
Hello All,
I hope that everybody here is able to view
HI Barbara,
This does look like an great web-site. I m going to check it out
further and already bookmarked it for future reference. I also need to
get moving. I've been eating too many calories lately and need some
motivation to stop eating potato chips and start lifting some
that reminds me of the hand brace I was given shortly after my attack.
It was brought to me because I was holding a rolled-up pair of socks to
soften the grip of my clenched hand. I didn't want to let the nurse
take the socks away. A therapist soon brought me a plastic hand/arm
brace that
Jim
I tried it. It is amazing and enlightening. I'll be sending this to a
few people including my nephew who is in in school to earn his
commercial pilot license. Thanks for sharing.
Patti - Michigan
On Tue, Feb 7, 2012 at 3:57 PM, James Berg wrote:
I usually don't forward things but
Rob,
I read this when you first posted itand reread it today. It's good,
true, and enlightening. I have also met normal looking TMers and
realized how hard it would be for a non TMer to know what we endure. It
allows me to forgive others and myself for trying to put normal in a
box.
Jim.,
I googled the wors incomplete spinal cord injury a came across a web
site that might answer you question regarding the chance for leg
movement and use after a sci. I've had TM for eight years and am always
amazed at the info we have at our finger tips. The articles were short
and
John
Whether it was a typo or on purpose the mental picture of a super bowel
made me smile before I even read your punch line. Then I wondered why
you picked Michigan's Detroit Lions team who struggled for many years
and could see them running for a touch down in their blue and white
Gilly
You are right to remide us about cothes, shoes and sock contributing to
our TM pain. I think I've posted for eight straight winters that
wearing blue jeans in cold weather puts me right to bed due the the
intense pain the cold material causes. New TMers beware! It isn't just
the heat
Thanks Jim'I'll look into them. I fell into the donut hole in
December 2011. I ordered my husbansds meds from Canada for five years
until he turned 65. We will both be in the donut hole in 2012.
Patti - Michigan
On Fri, Dec 30, 2011 at 4:05 PM, James Berg wrote:
Gerry and Pati--you
Gerry,
Many of us faced the same thing. Movement and feeling also brought the
feeling of pins and needles.
I've taken Lyrica for about three years - it helps a lot. I don't know
about side effects except the cost can empty your wallet. I would have
stuck with gabapentin, but it was
My husband also had no vitamin D and was put on 5000 IU daily. I tested
ok to the surprise of the Endocronologist who promised me that I would
be low, because we live in Michigan. I spend as much time out-of-doors
as possible in the summer. My B12 is always OK too.
However, I just added a
One of the best tools that I have used in talking to my doctors is
repeating something that I learned from someone in TMIC, my online
support group. I quote some of you. I ask my doctors about the meds
some of you are taking. I Show the combinations that are working and
let my doctor that
That's a good reminder Rob. We have to remember that we are also aging
or we could be causing injury to our bodies due to bad posture or the
wrong way of stretching due to our crooked bodies. A few years ago I
had to go back to PT for a frozen shoulder and it was fixed 100%. It
wasn't TM
We are fighters. Stress always aggravates my symptoms. You don't have
to disclose everything at once if you symptoms are stagnant. My
neurologist told me, Status quo is good. Anytime you aren't going
backward, going forward is easier. Simply disclosing that you had an
illness that left
Hi Cheryl
Glad to hear you and Mitzi are surviving the storm. It seems there is
always something to pull those dollars out of our pockets or checkbooks
or wherever we manage them. Your area sure has been hit with a lot of
storms. I hope your back home and warm soon.
Patti - Michigan.
On
HI Susan,
Thank you for the information. I smiled when I read your diagnosis of
Brown Sequard Syndrome, because it reminded me of the first time it was
used by a neuro in my presence. I was seeing the neuro who diagnosed me
in the hospotal with TM but his office was 70 miles away. I asked
Gary,
I hope your out-of-town siblings know and care how much you are doing to
keep your Mom and Dad comfortable in their old age. You must be
exhausted. You certainly have a full plate. Are you working also?
Pati - also in Michigan and watching the leaves faling one after another
-
You answered a question I hadn't asked. I wondered if anyone had gotten
shingles since TM. How nasty to have two causes of pain at the same
time. (I had a bee sting this summer that caused major pain for about 5
days. I laughed that it took my mind off my TM pain for a while.)
Patti -
Our local newspaper has a medical column in the Sunday edition by Dr.
Anthony Komaroff.
www.ask doctor k.com Sunday had a column titled shingles vaccine is a
good idea for adults over 60. A healthy 65 year old woman asked - what
is shingles and should I get the shingles vaccine. The doctor
Andrea,
You are a special spouse - searching the 'net for answers and asking how
you can help show how much you care for you husband and the future of
your family. I have had TM for eight years and have constant pain.
However, I enjoy my life in spite of it. I had a good neurologist who
I have those same thoughts when I read the things Akua goes thru day to
day. I remember the first time I went grocery shopping after TM. My 76
year old (at the time) Mom took me and a 9 year old boy carried the bags
from the car to the house. I would do your grocery shopping if I lived
Jane,
I'm sorry for the loss of your son, Chris. God will sustain you thru
this difficult time. Stay with us and know many TMers will be lifting
you up in prayer as you mourn the loss of both your son and daughter.
My condolences to you.
Patti - Michigan
On Thu, Oct 6, 2011 at 6:10 PM,
Dalton
You mentioned that you have muscle stffness when rising from a chair n
the same post you when you said you are now taking Lyrica instead of
gabapentin. I think I remember that as being a possible side-effect,
but shrugged it off, because it would not stop me from taking Lyrica for
Congratulations on your retirement. I know I've said it before, but I
can't imagine working while having TM. I think skydiving is the
ultimate gutsy thing to try. I'm not that gutsy, however, I went white
water rafteing this spring and found it to be exilerating.
Patti
On Tue, Oct 4,
Hi
I got booted off tmic several months ago by the computer phantom that
does that every once in a while and decided not to sign back up for
various reasons. I signed up today because I visited with David and
Judy Hoops , aka Hey Jude, today and we talked about how long it had
been since we
I am never pain free, however, I have moments when I didn't think about the
pain. Then shazam !
Patti - Michigan
john snodgrass jcs...@yahoo.com wrote:
Does anyone ever have moments that they don't feel anything?
Moments of no pain but then you move and shazam! there it is again?
Dalton
Thank you for the info on Omega 3's I know there are many reasons to boost our
intake, but I didn't remember that better mood is one of them. I'll set them
out for my hubby to take starting today (no kidding) and yes, I'll take them
too.
Your entire post is interesting, but your last
Prayers, antibiotics, food and fluids have all helped Jude recover from her
latest UTI. I talked with her tonight on the telephone and I'm amazed how well
she sounds. Jude does not remember my visit last week. She was surprised when
her husband told her I had visited. That's how sick she
Craig
Another hearty welcome to the TM family. Yes. the higher temperatures increase
my TM symptoms. Everything intensifies. The burning pain feels hotter, the
banding feels tighter, my bad leg feels heavier and I stumble more. Oddly, the
clonus in my hand is more pronounced and my fingers
Our prayers are being answered and Jude is responding. David said she has
become more talkative and is eating better. He sent me a note on facebook that
she requested a grilled cheese sandwich for breakfast this morning. Ahh.
comfort food!
I know I don't need to ask you to keep praying.
Ok Gunny, now I have goose bumps from reading your story. Thank you for your
service to our country. Your DI gave you a great piece of advice. We should
dwell on our abilities an use them for the good of others. Thanks for sharing.
Patti - Michigan
bgunny7...@aol.com wrote:
I was
I visited with Jude this afternoon and shared your prayers and well wishes with
her. She smiled when I mentioned that I had several responses from the group.
I reminded Jude of her post Does anyone remember Jude. She admitted that she
heard from people, but didn't respond. I'm not sure if
I talked with Jude's husband, David, this evening after receiving a message
from him that she is in a hospice program. David said she went to a hospice
camp for ten days and came home feeling better last week. Then she woke up
during her first night home with a headache and has gone down
I take 10mg Baclofen every 8 hours. This amount causes the least amount of
mental confusion and drowsiness.
Patti - Michigan
Like Gerry's news, the high temps and humidity in Michigan have made my TM body
miserable. Within minutes of going outside my skin feels like it is on fire,
my legs feel like petrified wood, my muscles spasm and every joint hurts. TM
won yesterday and today - and it hurt. I'm looking for a
The first doctor discharged me from ER even tho I was getting progressively
worse. Hubby took me to another hospital. They admitted me, I had a Neuro the
following morning, MRI in the afternoon and the steroids were waiting for me
when i got back to my room. I'm so thankful it turned out
Great discussions going on:
LYRICA
I took 1800mg Neuronton, then 2400mg, then switched to Lyrica because the
neurontin took too long to work and stopped before my next dose. The Lyrica
works faster and steadier at 100mg / every 8 hrs. My Neuro suggested this
switch when I complained of the
Rob
I think I was typing my last post wile you were sending yours.
I take Lyrica and Cymbalta and must also take Baclofen for the banding and
muscle spasms.
Lyrica and Cymbalta decrease the neuro pain, but he Baclofen is the first thing
I reach for when I've over exerted and my mucles are
Jeanne
I asked my doctor about a generic for Cymbalta because AARP sent me a letter
suggesting I try a generic to help cut my copay costs. I don't have the name
they suggested in front of me, but my doctor said it was the generic for
Effexor and it wouldn't give me any relief with the neuro
Jil,
That much neurontin also exhausted me, but I took fewer naps as time went on..
It never eliminated TM pain, however, it helped some. My biggest complaint
about Neurontin is the time it took to work and how fast it wore off. My Neuro
said that was a common complaint and suggested I try
Jeron
There is no fault with TM. You didn't do anything to deserve this and
couldn't do anything to avoid a recurrence. It sounds like you have a
neurologist who is on top of things and knowledgeable. Let us know what
treatment you are getting and know many of us are praying for a quick
The American Pharaceutical companies obviously have Google and MSN under their
thumb. Goodsearch still shows the Canadian drug sites.
Thanks Candy. I didn't know this was going on.
Patti - Michigan
CANDISKALLEY cakal...@embarqmail.com wrote:
I received the
I am amazed byal l of you who are able to work (as in paid employment). I am
ambitious, but can't imagine working to a schedule. My hat is off to each of
you.
Patti - Michigan
Butcher wrote:
With TM, it started with shoulder pain, went to doctor he found
weakness in left side,
Well, I talked with my doctor. He's a glass is half -full kind-of-guy. He
said to consider it an experiment and that now I know whether the benefits of
Cymbalta outweigh the side effects. Cymbalta is out of the system in five
days. So when I took it on the fifth day I learned know how much
Sitting in the evening is also my worst time with burning. It's not from the
inactivity. I'm actually paying for the daily activity and the burning pain
that I could ignore while I was busy. I imagine cutting off my left leg at the
hip to rid myself of the pain.
Patti - Michigan (now you
I'm here too?
I reduced my Cymbalta by 30 mg in December for a few reasons.
1. I didn't want to drive the 70 mile round trip for samples.
2. I didn't want to pay full price at the pharmacy.
3. I wasn't feeling bad, but I also wasn't feeling good - just kind of
unemotional
I stopped my
Very nice Mindy. Thank you for sharing.
Patti - Michigan
Mindy King we4king...@verizon.net wrote:
As promised last fall, I finally edited and posted whiter shade of
pale to Youtube and Darkness , Darkness as well
a Whiter Shade of Pale Darkness, Darkness.mov
Mindy the Artisan
Barbara
I'm a craigslist fan too. I bought quite a few items this way. It's sure better
than paying full price. Our daughter got me started using it and I sold a
few things last summer.
Exercise has been on my mind now that the holidays are over. We looked at
ellipticals last week and decided
Janice Nichols jan...@centurytel.net wrote:
How high up did you all get hit by TM? Give me the part of the body, not
the #.Thanks, Janice
From: Barbara H.
Sent: Saturday, January 09, 2010 10:40 AM
To: randy rankin
Cc: tmic-list@eskimo.com
Subject: Re: [TMIC]
Hi Janice
I was hit at C4-C6 - just above the bend when I tilt my head backwards.
Grace sent a good spine map that I'll try to forward
Patti - Michigan
Janice Nichols jan...@centurytel.net wrote:
How high up did you all get hit by TM? Give me the part of the body, not
the #.
Date: Sat, 17 Jan 2009 13:11:19 -0500
From: Grace M. grace...@gmail.com
To: tmic-list@eskimo.com
Subject: [TMIC] Spine Map (From Jim Lubin's Makoa site)
*This map provides a very rudimentary explanation for different segments of
the cord. It's from Jim's Makoa site. You might have to
Yes. My lesion was at C4-c6. I sometimes get exactly that feeling when I
reach with my right hand. It feels like I have grasped a live wire and makes
me think twice about what I had just done. (Did I just stick a fork in an
electrical outlet?)
I do not have (LeHermittes -sp?) tingling when
I'm here also. I think the holidays and the cold have caused us all to sit
quietly and wait for someone else to do the responding. Janice is good at
asking questions that get responses. Linda, what is your question?
Patti - Michigan (cold as usual)
L T CHERPESKI cherp...@msn.com
Peggy
Thanks for your post. I agree with you and support what you are saying. I have
bad days when the pain seems unbearable and I'm gritting my teeth, but then God
gives me the break I need. I put my hope and trust in God. I take meds, see
doctors, search the internet, ask my TM family and
Barbara, I'm glad Daniel has improved enough to come home. What a Christmas
present. Eight days of waiting must have really tired you out. I hope you are
able to rest. I will continue to pray for Daniels healing and for you also.
Blessings to you,
Patti - Michigan
Barbara Alma
I'm impressed Bobby Jim. I know a lot of men help in the kitchen - my Dad did
and my son-in-law does. Somehow I slipped-up in training my hubby!
Regardless, I thankful for him. (He offered to take me out last night for
supper.)
Patti - Michigan
bobby jim elbobber...@earthlink.net
I'm guilty of reading the postings without commenting. I'm guilty of spending
too much time on the computer - including facebook. However, I really got hit
with the guilts when I saw the birthday wish to Judy (Jude).
I was supposed to tell everyone that she is well and everything has been
I saw a group of six to eight touring Washington DC on Segways and thought they
looked liked the way to see the outdoor sights. I read the Segway pamphlet
regarding age and physical requirements and it stated that the person needs to
be able to step on and off quickly and wondered if this
Linda,
I forgot about the shoes. Let us know what you think of them. Of course,
Gracie wouldn't steer us wrong.
Patti - Michigan
L T CHERPESKI cherp...@msn.com wrote:
Janice, you're so funny. I might add that you've got a lot of company here
regarding the age category Ha - I've
Hi Mindy
I also enjoyed your singing, but didn't comment. I don't have a special voice,
yet I know God really, really loves to hear me sing! Really!
My 3 yr old grandson was walking around the house Sunday singing rejoice,
rejoice as he was playing. I had chills when I read my daughter's
I'm afraid to try them. I know you're all addicted! Maybe this winter when I
refuse to go out in the cold!
Patti - Michigan
Gillian Clark mingalett...@activ8.net.au wrote:
Games Janice?? Games you say!!!
A never ending amount!!
hugs
Gilly
- Original
I was gven a rocker- knife in rehab that I brought home with me. It has a big
rubbery handle and an oval shaped blade. Food is cut by rocking the blade.
I no longer need it, however, I have bought some kitchen utensils with larger
handles.
Patti - Michigan
CANDIS
It would be extremely helpful to those of us with sporadic memory problems if
everyone signed where you are from with each post. I started doing it when I
realized I'm not the only Patti. (Yes, there is only one Gunny, but for some
reason I thought he lived in Texas.) My 2 cents.
Patti -
It's exciting isn't it?
I met Heather from Calgary after two years of emails and phone calls.
I met Jude while she was sick and then got to watch her get better and
I had the priviledge of meeting Carol and her precious Jim who just passed away
as well as Lynne Meyers and two others at a
I take both Lyrica and Cymbalta, however, I also take Baclofen.
I take 100mg Lyrica x3, 10mg Baclofen x3, and 60mg Cymbalta in the morning,
30mg Cymbalta in the afternoon. I tried an increase of 120mg Cymbalta in the
morning and got brain zaps (Google the term - it's not fun) so I dropped back
I take both Lyrica and Cymbalta, however, I also take Baclofen.
I take 100mg Lyrica x3, 10mg Baclofen x3, and 60mg Cymbalta in the morning,
30mg Cymbalta in the afternoon. I tried an increase of 120mg Cymbalta in the
morning and got brain zaps (Google the term - it's not fun) so I dropped back
Same with my family. Daughter works in a hospital, her husband in a clinic and
grandson goes to pre-school. All three get flu shots, she gets the pneumonia
shot.
Patti - Michigan
Patricia Cooley patticoo...@wi.rr.com wrote:
JUDE I THINK EVERYONE, WITH THEIR DOCTOR, WILL HAVE TO MAKE
I qualify as a member of the TMer BMer club. I hope this is an honor-system
membership with no proof requirements.
My Neuro and his family get annual flu shots. He advised me to get the shot -
yet I haven't done so since TM and likely won't. I didn't have a shot the year
I got TM, but
Connie,
I take 10mg Baclofen 3 times daily and 100mg Lyrica approx every 8 hours.
I think the Baclofen helps the most with the banding and know I would be bed-
ridden without it. I've been on Baclofen for five years and on this dose for
the last three.
Patti - Michigan
connie markovich
This is amazing. I'm speechless.
I hope you will continue to gain movement in your thumb and hand. I believe in
miracles.
Patti - Michigan
Jim Lubin jlu...@eskimo.com wrote:
I've had TM for five years and don't expect an MS diagnosis. I've had the
banding trom the beginning. During one of my steroid IV's (first five days) I
rang for help and told the nurse I couldn't breath and something was squeezing
my chest. It was painful and I asked her if I could be having
Hi Peggy
I have stiffness and problems with my hands due to the TM lesion at C4-C6.
Like Jeanne,I don't know how much to blame on TM, age, weather, room
temperature, or what I'm trying to accomplish. I use a heating pad to keep my
hands warm while watching TV in the evening and I have a rice
Yes, I can move my fingers. I'm right handed and that is the hand that is most
affected. I hadn't thought about my joints being stiff, but my hand movement
is sluggish and I don't have normal sensation or feeling in most of my fingers.
I can grasp items, but have difficulty fingering. I had
Amanda,
I have chills from reading your story and I think they started when I read that
you can wiggle your toes. I hope you continue to acquire movement and will
keep us up-to-date on your accomplishments. I was still healing at nine
months and pray that you are too.
Patti - Michigan
Has anyone seen a therapist, psychologist, psychiatrist, etc. for depression
since being dignosed for depression? Did it help you?
Has anyone been on Cymbalta and switched to another antidepressant?
For those of you on Cymbalta - are you on it for depression or pain or both and
how much do
Thank you Akua for allowing us to read from your heart and soul. Brilliant! I
read them several times, because your words say so much! I'm not in a chair and
feel that you added so much insight as to how it is for you. You should be
published . Oncore!
Blessings
Patti - Michigan
Akua
Linda,
Heather and I were just talking about our inability to stand with our heads
tilted back without loosing our balance.
Patti - Michigan
L T CHERPESKI cherp...@msn.com wrote:
Heather,
I haven't given up yet, but I still can't look up at the stars without
almost tipping
Akua,
Can we read any of your poems? I would like to and I think others would too.
Patti - Michigan
Akua a...@artfarm.com wrote:
thanks Linda, and the neurologist is a she!
Akua
Congratulations Akua! What a huge accomplishment. I can relate to
the neurologist challenges, and am
You made me laugh. Thank you for too much information. I've never had any
of those experiences. I'm glad your feeling better.
Patti - Michigan
balmat...@aol.com wrote:
Tried the Zanaflex and didn't work well for me.? It relaxed me too much, and
when I finally got to the bathroom, I
Jeanne
That was a compliment and I would have responded I take that as a compliment,
thank you. or it could have been an original pick-up line.
Patti - Montrose
jrushton jrush...@columbiaenergyllc.com wrote:
Jack and I had gone somewhere where there was a crowd and this one guy
walked
Catherine
I replied to Melissa about my experience of buying two pairs of leather oxfords
to wear with my AFO in the winter. I thought everything fit fine, however, I
injured the top of my foot, because there wasn't enough flexability in the top
of the shoe. I recently used it in a pair of
Hi Marie
I'm glad to hear you've been able to talk with Jude. Yes, she is a wonderful
woman. I'm also glad you're able to read all of our posts and keep up with
such a great group of wounded people. I often think the pain is the worst
part of TM. I'm always happy for any TMer who has been
Hi Sandy
Welcome back. I'm glad you had your vacation and hope you have lots of pictures
for Terry to review during his recovery. He'll be your handsome bionic man
soon.
I'll be praying for a successful surgery, speedy recovery and pain-free days
ahead.
Patti - Michigan
Hi Betty
Welcome to our on-line TM family. I was diagnosed in 2003 at age 53 at C4-C6.
I also have balance problems and just gave in to using a walker during a short
vacation. I was surprised that I was able to walk and enjoy looking at
something besides my feet. I hadn't thought about the
Hi
Jude came home on Monday. I called her at home and asked if Ella was typing
her note at the same time she and Jude were talking on the phone and she was.
So Ella, thanks for the great news and it's ok if it was a little confusing.
Jude has been trying to type to the list and hasn't been
AMANDA,
Thanks for that info, It is the fat cells that Jude and I wanted to donate to
research. Now we have a reason to hang on them afterall! I'll have something
to laugh with her about!
Patti - Michigan
Amanda Diskey adis...@yahoo.com wrote:
I did not add that the stem cells they
Frank,
I hope you heal well and that the worst is behind you. Spring is comming soon
so sitting in the sunshine will be an option in your healing process. Are you
typing one-handed now? Keep in touch even if you only type I'm here.
One-armed hugs,
Patti - Michigan
I talked with Jude Wednesday evening by telephone, because I had a sore throat
and runny nose and couldn't visit her in person. She had been on the phone all
afternoon with other TMers (as Jude would say -you know who you are) and said
she realized that her last message sounded like she was
Janice,
I got goose-ubmps reading your note to Jude. This is exactly what the list is
about and why we are so glad to have new members who can join in inspiring each
other thru the hard times of our TM journeys.
Patti - Michigan
Janice jan...@centurytel.net wrote:
Jude,
I am new to
Hi Jude,
You write beautiful and inspiring notes. I don't know where everyone is and I
also miss having lots of posts to read when I check in. I think there are many
of us who read, but sit quietly by while waiting for others to answer the
questions that have been asked.
March 20th sounded
Hi Deb,
Welcome to the group, although, it sounds like we all had a mental melt-down
when you first approached us. I'm glad you tried again. We need fresh faces,
ideas, reminders and medical news. Sometimes it is the newcomers who give us
oldies the push we need.
I am always impressed with
Date: Mon, 9 Mar 2009 11:24:32 -0700
From: pjv1...@chartermi.net
To: tmic-l...@eskimo.org
Subject: Update on Jude
I have an update on Jude, however, sometimes thing move so fast with her that
my updates are out-dated and I don't even know it myself. I hope Pam or Ella
will post if
You reached the TM internet club site. Welcome to a great bunch of people who
are eager to help each other with questions and answers regarding Tranverse
Myelitis.
Patti - Michigan
Janice jan...@centurytel.net wrote:
This is a test for correctness of address.Please reply.
I currently buy meds for my husband thru a Canadian site and save 1/2.
I was very apprenhensive when I started, but have had no difficulties in the
two years of doing so. I'd be happy to share the info with anyone who needs it.
Patti - Michigan
Patricia Cooley patticoo...@wi.rr.com wrote:
Gerry,
You made me laugh. I would never have thought of NFTA and snow together! Now I
wonder where Global Warming fits into the picture. I liked your little typo- I
got stuck on wondering what a wetmer was. (Wetmer's, what's a wetmer?) I
thought it had something to do with NAFTA until I
I'm not a Soc Sec expert, however, This is what I know:
It took me 18 months from the time I filed until I was approved for Sos Sec
Disability Income and have been on it for 3.5 years.
I have a right to Work Ticket that allows to attend school or seek training
for employment or to work.
Happy Thanksgiving from Michigan to my TM Family.
I'm sitiing here relaxing (the turkey is in the roaster and the Macy's
Thanksgiving Day parade in on the TV) and wanted to say Hi to all of you, or
as I would lovingly say it in person, Hi, ya all!
Blessings
Patti - Michigan
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