Foot Drop

It's a daily thing I wake up go to the bathroom then the pain starts. It feels like I was hobbled over night because my ankles,my feet, and calves are dysfunctional causing feet and hand deformity. The genetic disease i have will progressively take out all type 1 skeletal muscles.

There is a cardiac involvement but I'm awaiting to see Cardiologist at Cedar Sinai to evaluate the pathology of my variant.

Ten yrs and eight spinal surgeries gave way to neurogenic muscle atrophy and beginning this year finally diagnosed with muscular dystrophy at 58yrs old. I have been wearing full leg braces due to bi lateral foot drop for over 15yrs.

Don't know why I posted such a detailed description and to whoever reads this I'm grateful you took the time.Sometimes because of my age I don't think me or my condition is important and that if there is ever a cure or treatment for this rare affliction it should be for children and congenital complications.#OCD #BPD #chronic pain#myocodritis #MuscularDystrophy #Peripheral neuropathy #MDD #

I joined this group a little while ago but didn't feel like using hashtags but I imagine for social forums that are geared for relatability it's a good thing so I decided to use hashtags but no need to respond just getting it out there.

#BPD #chronic pain#mobility problems #Muscular dystrophy #perpheral neuropathy #Hyperalgesia #OCD #distal and proximal myopathy #Facial neurolgia#bi lateral foot drop

Hi, my name is Kim Meinerth. I turned 70 last Spring. I have worked for major computer and graphics companies since 1978. I currently live in south Santa Clara county, CA. I am currently working for AMD as a Senior Fellow System Architect. I've been diagnosed with Primary Progressive MS this past summer. I am currently on medical leave to focus on my health.

Vertigo started in my early 30s with week-long episodes. I believe that my balance started to deteriorate then too. Had an MRI (1985), but my Neurologist in MA could not find MS lesions. He did find an issue in I believe my brain stem. Had a spinal tap and found no signs of MS.

In early 2018 Stanford HC MS specialist neurologist Dr. Lock studied the 1985 MRI and found the MS lesions.Dr Lock confirmed my MS diagnosis with more brain & spine MRIs in early 2018.

I also had a bad case of mononucleosis in 1971 that was likely the trigger for my MS journey.

We believe that my walking gait issues started in my early 40s. Balance started getting very bad, as well as, weakness, pain in my left hip, ankle. Foot drop and swinging my left leg out to avoid tripping developed later. Progression was very slow and I did not notice it until I started tripping and falling with friends asking me what happened to me.

Left arm and hand weakness started in my 60s. Left arm and hand numbness, weakness, no coordination started in June of last year after 3rd Covid virus. Left leg and arm got significantly worse with each of my 3 Covid viruses.

I was diagnosed with Primary Progressive MS this past summer 2024.

Vertigo seems to always be the result of intense stress, mostly self-imposed from my career.

I am looking forward to joining a MS support group.
Kim

#MightyTogether #MultipleSclerosis

Hi, my name is delightfulgal4. I'm here because I was born with hip dysplasia and have had hip surgery at 48. Last year May 2022 I dislocated my knee and my peroneal nerve was severed. Now I have foot drop and have to wear an AFO. not the easiest but it is helping me with my gait and lifting my foot

#MightyTogether #HipDysplasia

I’m new here. Interested in #spinal #Fusion #mobility #Neuropathy
#FootDrop content and connections

I was a new Mom in 1998 and a nurse who worked in the ICU with a very physical and demanding job. I sought help with the pain I had in my right leg. I was worked up for Lupus due to a positive ANA but nothing really ever came of it. I would have right hip pain off & on through the years but chalked that up to the 12+ hour shifts I worked due to being physical the entire shift and fatigue from working long hours. I was then a mother of 2 who had a house to take care of.

In 2015, now a Nurse Practitioner, I decided that I would train for a marathon. I had some musculoskeletal problems during that time, of which I self-diagnosed with chin-splints, worse on the right. I developed a foot-drop like problem when trying to speed walk, most noticeable in late 2017 that started a workup of being diagnosed via MRI that I have a torn hamstring on the right so we chalked that up to an injury in high school and focused on physical therapy.

Enter 2022, the end of the COVID-19 pandemic: at the beginning of that year I noticed my right calf was smaller than the left. I knew as a practitioner that was not right! So I went for a second opinion with an Orthopedic provider who told me I needed to see a Neurologist. I was actually mad at him at first because I thought that he was rude and I felt put-off. However, he was just honest telling me that he did not know what the problem was and it was not an Orthopedic problem.

My great and compassionate Neurologist assured me that she would get to the bottom of things for me and I was diagnosed with MS in November 2022.

What’s my take away: Take care of yourself – do not ignore yourself! Be persistent and be your own advocate!

Hi, my name is mrsjmpa. I'm curious about living with chronic pain, sciatic nerve injury, foot drop palsy, depression, anxiety, and parenting a young adult child who became blind in late teenage years.

#MightyTogether #Depression #Anxiety

I have been having problems with my right knee. I had a knee scope November 2022. I thought everything was ok, until I couldn’t move my toes and I all of a sudden I could walk I had a tingling and numbing sensation on the right side of my body. I went to the emergency room January of 2023 to find out I have foot drop and he recommended me to go see a neurologist. Went to go see a neurologist she said after she did an exam on me, my right side side of completely weak and I was showing signs of Multiple Sclerosis. Ok boom she wanted me to go to the emergency on a Monday Morning so I can start my high dose of steroids. The steroids worked miracles but when I was discharged I started back dragging my foot and could barely walk. I am excited to say
#MultipleSclerosis

I just started the MS medicine Aubajio today, and I'm looking for feedback from people who are taking it. Want to know what I might to expect as far as side effects or any information about experienced feelings. I have been hesitant about taking any medicines at all, hoping that I that my MS would stop any more progression. I got misdiagnosed in 2014 and it raised its ugly head again in 2018. I started taking Copaxone then but had a reaction of shortnees of breath after a month, then stopped taking it. It's taken me this long to start taking this after what I would call a couple of relapses. Hugs, and foot vibration. My main symptom when it started was foot drop and muscle weakness. It hadn't advanced much until lately so I'm going to try again hoping for some relief. Like I said any information would help. Thank you so much.

Hi, my name is debzhancox. I'm here because i have been diagnosed with CRPS in my left leg just above the knee down to the tips of my toes. I also have CRPS, Dupuytren's contracture and Osteoarthritis in my right hand/wrist. im currently in a wheelchair as im unable to weigh bear on my left leg, its very stiff resulting in being unable to bend or straighten it, its stuck in a slight bend and i also have foot drop

#MightyTogether