Ohhh the life of a CMT'er!!! To try over and over again to find a set of medications that may help improve our quality of life, battle constant chronic pain and possibly lift us out of our chronic fatigue. I have searched high and low for different doctors, different types of doctors, new meds and I'm still searching for something that will help me - as I am sure are many people with CMT and other neuropathies.
One of my fellow pool therapy buddies recommended I go see her pain management doctor who helps her a lot and he is located in the next town over so I figured I should give it a shot. I made the appointment for yesterday and the hubs came along with me (it's always good for me to go with someone because I can NEVER remember everything I plan to say or ask).
We arrived for the 12pm appointment and weren't called in to the office until 1:30pm!!!! This is one of my BIGGEST pet peeves. What is the point of scheduling a time if you're going to keep me waiting so long? And, in case you missed it, I am going to see the doc for pain, so to leave me waiting that long is not making my body feel any better. We almost asked for the co-pay back and walked out when they finally called us in. My first impression so far was not good.
Thankfully, the doctor was very nice and helpful. I am only his THIRD CMT patient ever (Shocker!) - I am just glad at least that I wasn't the first! He listened to my entire history and we begun discussing what could possibly work and what approach I should take. At the end of our chat, we have added 4 new meds to my daily routine to start off with - well, 3 new meds and 1 vitamin. Two of the meds are for pain and one is for chronic fatigue, which is honestly the one I'm most excited to try.
I am cautiously optimistic about the possibilities and hope at least one of these will help me find some relief. The plan is to try them out for a month and go back to him for a follow up. I am crossing my fingers that I have good news then...wish me luck!
skip to main |
skip to sidebar
My life with CMT and trying to deal with constant chronic pain with a positive attitude...
Thursday, May 17, 2012
Subscribe to:
Post Comments (Atom)
About Me
- Michele
- CT, United States
- I'm a girl with hopes and dreams who has Charcot-Marie-Tooth (I know! You've never heard of it!). In this blog, I talk about my journey with this invisible disease and 2 reconstructive foot surgeries (and a 3rd minor surgery) I've gone through in the last 18 months. And I try to do it all with a positive attitude and a smile on my face :)
Highlights of My Journey
Followers
Labels
- A Slice Of Hope for CMT (3)
- America's Got Talent (1)
- Anesthesiologist (2)
- anti-inflammatory (1)
- bernadette (7)
- Birthday (1)
- Blog (2)
- Callus (11)
- Care Taker (1)
- Cast (7)
- Catwoman (1)
- Charcot-Marie-Tooth (67)
- Charcot-Marie-Tooth Association (10)
- Charcot-Marie-Tooth Awareness Month (2)
- Chipotle (1)
- Chronic Pain (7)
- CMT (79)
- CMT Awareness (5)
- CMT Awareness Month (12)
- CMT Awareness Week (2)
- CMT's Fab Five (3)
- CMTA (9)
- CMTA Awareness Week (1)
- CMTA STAR Research Program (2)
- Commode (1)
- Connecticut CMT Support Group (4)
- Constant Pain (13)
- Country Music Television (1)
- Crutches (5)
- Cyber Monday (1)
- Depression (2)
- documentary (2)
- Dr. Daniel DiCapua (2)
- Ellen Degeneres (1)
- Exhaustion (8)
- Faith (8)
- Fatigue (9)
- Fifth metatarsal (1)
- Foot Deformity (2)
- Foot Surgery (28)
- Frank Sinatra Park (1)
- Frustration (3)
- Fundraiser (1)
- Governor Christie (2)
- Governor Malloy (2)
- Hammer Toes (4)
- Having Mountain Moving Faith (1)
- Hereditary Neuropathy Foundation (3)
- High Arches (6)
- Hormones (1)
- Hospital for Joint Diseases (7)
- I Am A Star Award (1)
- IASP (1)
- Insurance Company (2)
- International Association for the Study of Pain (1)
- Invisible Disease (2)
- Ivete Sangalo (1)
- Jocelyn Maminta (1)
- Joel Osteen (1)
- Journey (2)
- Leg Pain (8)
- Lenka (1)
- Lyrica (3)
- Marketing (1)
- Massage (1)
- MDA (2)
- MDA Loan Closet (1)
- MRI (1)
- Muscular Dystrophy Association (2)
- Natural Medicine (1)
- Nerve Pain (6)
- Neurologist (6)
- New Foot (8)
- New York Botanical Garden (1)
- Newport (2)
- Numbness (2)
- Nurse (1)
- Oprah's LifeClass (1)
- Orchid Show (1)
- Orchids (1)
- Orthotics (1)
- Pain (16)
- Pain Management (9)
- Pain Medication (11)
- Percocet (1)
- Physical Therapy (12)
- Pictures (2)
- Pills (1)
- Podcast (1)
- Pool Therapy (3)
- Power Chair (1)
- Prayers (3)
- Presents (1)
- Professional Services (1)
- Radio City Music Hall (1)
- Reconstructive Foot Surgery (7)
- Recovery (10)
- Recumbent Exercise Bike (2)
- Rhode Island (1)
- Scooter (2)
- Shelton Herald (1)
- Shoe Lover (1)
- Steroid Injection (2)
- Stitches (2)
- Supplements (1)
- Support (3)
- Surgery (10)
- Swelling (8)
- The Indie Chicks (1)
- The Spoon Theory (1)
- Tramadol (1)
- Valley Independent Sentinel (1)
- Visitors (2)
- Vitamins (1)
- Voices of CMT (1)
- Walker (3)
- Wheelchair (9)
- WTNH (2)
- X-Rays (2)
2 comments:
Ugh....I hate the "Dance of Doctors" as I call it. Hopefully this new one will be good, and the new meds will help! You'll have to let me know how the one for the fatigue works....that sounds intriguing!
Yes - also intrigued about your med for chronic fatigue! Love Melissa's "Dance of the Doctors" term - sadly, so true! Betcha the doc has had more than 3 CMT Pxs - they just don't know (because of lack of knowledge about the disorder) they have it...and the docs didn't think to investigate it. I loathe the idea of people going through life just thinking they are weak/lazy/accident prone when really they have CMT. Good luck with the new meds!
Post a Comment