jwggraham

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  • October 18, 2016 at 11:59 am

    Hi:

    While I was paralyzed with GBS I had no control over either bowels or bladder. 10 tears since I have no bowel issues but have had bladder stones removed twice. One was 3′ long. Problem is that I can’t fully empty bladder. Prostate is normal but it’s hard to go.

    September 15, 2007 at 9:41 pm

    Saw your reply to my One year aniversary. Glad to hear you are riding. When I’m on a bike I’m allways smiling. I live in Florida but if your ever down here give a shoult on this board. I’ve got two bikes. A 1997 Valkyrie and a 93 Goldwing. I love to ride and use the bikes as often as I can. No winter here – you have that issue in Maryland.

    Ride safe and keep the rubber side down.

    John Graham

    June 17, 2007 at 7:21 pm

    Rebecca:

    I have had GBS last year and am making a great recovery but when I saw your note about having Cipro the day before a neurlogic episode (thought to be GBS) I had to reply.

    I had a person working for me about 4 years ago. He was given Cipro for a cut (to prevent infection from a possible racoon bite). Within 8 hours he was in the hospital halucinating and they thought he was high on Oxyconten. Only thing he had taken was 2 cipro pills as prescribed. No other drugs at all.

    He had severe memory problems, was having difficulty talking (reversing words) and had a lot of wierd sensations in his legs. Tingling and he also had problems eating. Certains foods such as fish would cause the symptoms to re-appear. The symptoms persisted for about two years.

    There has been some research on the side effects of Cipro on people. Remember the people who took it here in the West Palm Beach area a few years ago when we had the Anthrax attack? The people complained about a lot of memory problems. They blamed it on the Anthrax (which many of them had no symptoms of) but I suspect it was the Cipro.

    I know there is a support group on the Internet of people who have had bad reactions to Cipro. You may want to do a search.

    Don’t expect any luck getting anyone to admit that there might be a problem with Cipro. My freind had no luck even though he couldn’t work for a couple of years afterwards. They just told him he was crazy. (Think liability.)

    Good Luck – let us know.

    February 27, 2007 at 10:18 pm

    Peggy:

    I feel for your brother. I came down with GBS on Sept 9th, 2006. While I never lost all sensation (and there were times I wished I had due to pain) I was paralyzed from the waist down.

    There is wide variation on how people get the disease and recover – this is how I came back to where I am now.

    Sept 9th – After a week with the flu, my abdomen became numb, I went to the hospital and collapsed that evening.

    Sept 12th. First day I remember since the 9th. I was totally paralyzed from my nipples down to my feet. Some feeling in legs but not much. Spent week in Intensive Care.

    Sept 19th. Moved to local hospital that deals in Spinal Cord Rehab. No movement as of yet.

    Sept 19th to Oct 25th. Blurry vision, hands become weak and tingly. Therapy is spent learning how to do board transfers (bed to wheelchair, wheelchair to bed). Very scary but I don’t get dropped. Also trunk excercises since I couldn’t hold myself up. Spend hours on the PT mats on my back with my legs bent trying to hold them up (and they keep falling over). Also had a lot of painful muscle spasms in my legs. Of course since this began I have hade no bowel or bladder control. Several episodes of fainting when sitting up. (This is common with spinal cord injuries apparently).

    Oct 25th – Nov 18th. Transferred to nursing home (actually an old folks home that does therapy). They use electro therapy on my legs and tell me to curl my toes when the electricity is on. This is the first time I see my muscles start to move. Just the toes and ankles a bit but at least there is improvement. Still working on trunk muscles without much success. Very severe muscle spasms in legs – every 8 seconds at times.

    Nov 18th. Sent home by Insurance Co. Have hospital bed at home. Can barely transfer to car from chair. Still incontinent. (this means diapers!)

    Nov 18 – mid December. Seeing more movement in legs. Have home therapy 3 times/week. Can turn a set of bicycle pedals with help from the therapist. They stand me up for 2 minutes at a time – it seems forever.

    Mid December to Dec 31. I can use my legs to turn over in bed. This is a BIG improvement since I would otherwise need help to turn from side to side.

    January 07 – Getting more strength. I can stand up in to a walker on my own. See improvement every day. I go swimming in a local pool.
    By mid month I can drive an automatic transmission car. I can transfer into bed or into car from the wheelchair without using the transfer board. Can get in to tub on my own. Also am able to sense when I need to use the toilet and get there (most of the time). I can cross my legs in the chair. This helps when putting on socks or shoes.

    February 1st to 15th – In therapy they have me using the parallel bars to walk. Also using a machine where you push pedals to do steps. I can drive a standard shift car. I can stand up to pull on my pants. I can sit up in bed by using my trunk muscles. Spasms are gone except in the morning when I stretch.

    Feb 15th to Feb 28th – Use the walker around the house for short distances. Can walk in to a restaurant with the walker. Working on trunk muscles in therapy.

    As you can see I did not see much improvement until after about 3-1/2 months. Then things started to progress at a faster pace.

    Don’t know how your brother will progress. However when I was in the hospitals and nursing home no one would give me any idea on “how things come back” even though I asked. There was no computer access either so I couldn’t look anything up.

    Hope this helps

    John

    February 27, 2007 at 9:39 pm

    Date – Sept 9, 2006
    Location – Jupiter FL (near West Palm Beach)
    Suspected cause – I had a nasty flu the week before. The flu seemed to be getting better and then got worse and I started going numb. Collapsed that night.

    February 24, 2007 at 10:46 am

    As one who is just now starting to walk with a walker 5 months post GBS I must say the video’s brought tears to my eyes. Great to see the progess he is making. Thanks for posting.

    John

    January 30, 2007 at 5:30 pm

    Miss 30 Days. We both got GBS in September so I know much of what you are going through. I was paralysed from the nipples down but did not need to have the trach.

    Hang in there. It does get better. I’m in a wheelchair but am walking with a walker up to about 80 feet and am feeling much better. The key thing I am getting from these boards is that you shouldn’t tire yourself out too much when doing therapy.

    You are young so we can hope and pray that you will have a good recovery. Take things one day at a time.

    Good Luck

    John Graham
    Jupiter, FL

    January 13, 2007 at 3:45 pm

    Rose:

    I know what you are going through. I saw very little improvement the first two months but am now seeing improvements every few days. I can’t walk yet but my legs are getting better and just beeing able use them to flip over in bed is a great help.

    I remember after 5 weeks in the hospital, asking if this was what the rest of my life would be like. The OT therapist assurred me that it would get better. I didn’t see how at the time, but life is good now and I am seeing progress.

    Everyone’s case is different but things will improve. Keep working on your therapy and be patient. It takes a long time before things start to improve but they will.

    John Graham
    Jupiter, FL

    January 13, 2007 at 3:15 pm

    I to am suprised at the numberof people who were sent home not being able to walk or even use their upper body to transfer from bed to wheelchair etc. Particularily since many had no one at home to help them.

    I have been doing well at home. I did not lose use of my arms or hands (although the hands tingle a bit). I learned to transfer from a wheelchair to a bed and vice versa in the hospital. They also trained me on going from a wheelchair to a car. I have a hospital bed which raises and lowers so that helps. I also have someone at home that provides excellent care for me.

    When I first came home I used a transfer board to get in/out of bed. However I have a friend who has been in a wheelchair for 15years and she showed me how to get in and out of bed without the board. I do it all the time now. I use my arms ( strengthened from all the weights I lift in PT) to do the transfers. I am also getting significant help from my legs now and this enables me to get in or out of the tube without assistance. Toes, feet and legs are comming back – in that order – but my trunk is still weak.

    Big step yesterday! I have been a private pilot for many years and while I sold my aircraft after getting sick, I have friends that fly. After getting the doctor’s OK, my friend took me to the Light Sport Aircraft show in Sebring yesterday. He has a Cherokee 6 which has a door to the last row of seats. It is low enough that I can transfer (with a transfer board) in to the aircraft. My friend then put the wheelchair in the luggage compartment and off we went. After being grounded for 4.5 months it was great to be in the air again. Brought tears to my eyes on the takeoff! The show was excellent. I was even looking at new aircraft since I hope to own one again someday.

    I was at the doctor’s office on Thursday and he thinks I will be walking at 95% of my previous abilities in 3-6 months based on my progress. (I had one doctor say I would never walk again period.) This is the first time they have made definitive statments about walking again! So far I have not been plagued by the fatique that seems very common amonst GBS victims.

    I’ve got a ways to go but the outlook is positive now.

    January 9, 2007 at 11:18 am

    Thanks for the reply.

    I did not have any digestive problems at all. In fact the meals in the hospital were what I looked forward to the most. However I did lose all control of bladder and bowels. I did get bladder control back after 9 weeks (hospitals used catheters, nursing home insisted on diapers only so I was motivated – particularly since they weren’t too fast about changing diapers.)

    Bowel control came back last week – thank heavens!

    I go for my first outpatient therapy tomorrow. They have a pool so I am hoping that I can use it. I did find a local municipal pool that has a lift to get me from the wheelchair in to the water and I am planning on going there this weekend once they open up for general swim instead of laps only.

    I see the doctor that treated me at St Marys on Thursday. He is not a neurologist but is a rehab physician specializing in Spinal cord injuries/diseases. Of all the doctors I have seen he is the only one I really trust. (Saw one neurologist that ordered a test and then never even gave me the results.) I did see a neurologist last week at the Clevland Clinic and they said to continue with the therapy and that no other treatment was required. Saw another neurologist in December who was amazed at my progress.

    While in the hospital I did have two regimens of Prednezone (which I think is the IVG.)

    I was able to get into the baby crawl position in bed this morning without falling over like I did earlier in the week. So I’m Getting Better Slowly.

    Hope this fills in the details.

    John Graham
    Jupiter, FL