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I AM SO HAPPY NOW IN MADDIE'S AND MY NEW APT. WE HAVE WONDERFUL NEIGHBORS AND WE TAKE CARE OF EACH OTHER. MADDIE WILL BE A YEAR OLD ON SEPT 27TH AND THE YEAR HAS GONE SO FAST. I HAVE THE TIME TO BE HERE MORE OFTEN PLUS WORRY ABOUT ME INSTEAD OF TRYING TO HELP SOMEONE THAT BELIEVES SOMEONE BESIDES ME ALL THE TIME SO NOW IT'S MY TURN AT LIFE AND I'M TAKING ADVANTAGE AT IT. I AM 53YRS YOUNG AND PROUD OF IT.
I AM SO HAPPY NOW IN MADDIE'S AND MY NEW APT. WE HAVE WONDERFUL NEIGHBORS AND WE TAKE CARE OF EACH OTHER. MADDIE WILL BE A YEAR OLD ON SEPT 27TH AND THE YEAR HAS GONE SO FAST. I HAVE THE TIME TO BE HERE MORE OFTEN PLUS WORRY ABOUT ME INSTEAD OF TRYING TO HELP SOMEONE THAT BELIEVES SOMEONE BESIDES ME ALL THE TIME SO NOW IT'S MY TURN AT LIFE AND I'M TAKING ADVANTAGE AT IT. I AM 53YRS YOUNG AND PROUD OF IT.
Living, loving and appreciating life every day, electronics, music, watching and feeding birds, meeting new people and talking to them and learniing new things because that\'s what our brains are for.
Living, loving and appreciating life every day, electronics, music, watching and feeding birds, meeting
I have asked others on the board and noone has heard from you. I'm very concerned, obviously, something is wrong. I pray for you everyday Gale. oxoxox Sandra
gale I am back and missed you so much, I got your email deleted so will message you and give you my new one. Tinkerbell is a beaut!!LOL
I am so happy you have your own place Gale. I know this was really answered prayer. You must have so much peace having your own place and the freedom of a whole apartment that you can get around in. It's amazing what your own home does for happiness, isn't it? Look forward to hearing from you when you have time honey! xxxSandra
I've gone over the rainbow. Come join me. Hope all is ok there. Later...Darlene
Hey galed
I have cronic pain as a result of Multiple Sclerosis. I have had very severe pain on and off over the years but not I have it and it won't stop. Am using an implanted Morphine Pump and feeling great where that excrutiating pain was.
Have gone through hell with this disease which started with a flu shot 24 years ago. Almost died 2 times and have had so many other illnesses because of this disease. Am now in secondary progressive stage of disease and need someone to talk to.
I got herpes symplex all through my body in January from a stay in the hospital. Right now I am having a relapse in my mouth since biting my tongue last week. I have a week immune system because of repeated sterodial use and picked it during a hospital stay for possible pneumonia in January.
i have had MS for 24 years and found out after 3 years of having this that I have it. No wonder I hurt all over and can't sleep. Here I am with another illness!!
I came down twisted on a trampoline and after tearing all my muscles and ligaments out found out I had DDD. I went to a Neurologist for this condition. That was long ago. If their not handling this now maybe a Bone Specialist or Rheumatologist. I know they wouldn't opeate no matter what when I was diagnosed
I was hospitalized because I didn't feel well and was having some complications from Bladder Surgery. It was hard to swallow and I couldn't sit because of the pain. In the hospital I was running a low blood pressure and then they checked my blood pressure lying, sitting, and then standing for several days. They found that my Adrenal glands weren't functioning right and then did a Cortisol Test. Then I was put on Florinef and sent home. I have MS and many other health issues.
Because Of me having MS, Fybro, and now Addison's I sleep so much. Even if I get to bed early I sleep until 5:00pm the next day. I also have chronic pain and have an implanted Morphine Pump but I have other pain from OA and Fybro.
I have on again and off again Anemia. I have it now. I don't feel like eating but use Ensure and eat a little. I've had both iron and B6/B12 Anemia.
I got this from having Allergies for many years. I have Bronchial Asthma. Doesn't matter what I use I still get lung problems from colds, etc. I use a mask all the time now also.
When I was 16 yrs old tore all the muscles and ligaments out in my back and ended up with bad back pain for most of my life.
I am 52 and have cataracts. They aren't that bad yet but the doc keeps checking them.
I had chemo twice to help get rid of an MS relapse. It didn't really help in my case so they stopped using it.
Iam a caregiver as we speak. I have been a caregiver since I got married because my husband is 24 years older than me. I also help my Mother and helped my Dad when he was alive.
I have been in a coma twice. First time for 2 days with a fever of over 104 caused by Septic Shock and second time 3 weeks caused by overdose of Dilauded given to me every 2 hours in my infusaport for over 2 weeks. While in the coma developed a pneumonia they couldn't identify so they tried antibiotics they thought would bring me out. Died while in this coma and the nurses got me back.
I have been depressed for 24 years from getting MS and then other diseases. Did die once and have been in the hospital over 90 times.
I got dry eyes several years ago. I went to the eye doctor and we tried eye drops with temporary tear duct plugs first and then when the drops weren't working and the plugs totally came out they put permanent plugs in and I haven't had a problem since.
When I got a flu shot in 1987 I got Encephalitis in my Cerebellar or the Brain Stem. Either that or the flu shot started the MS. I couldn't walk straight or type right. It eventually went away but it really affected how I moved and my typing ability.
I have had allergies most of my life. Between runny eyes, runny nose, sneezing and other problems from it I got asthma eventually.
My first cat's kidneys stopped functioning and I had to put her to sleep. I got her for my husband on Fathers Day and when she was 7 I found her between the wall and toilet. Her kidneys were failing and they gave her intervenious over the weekend then sent her home with 6 months to live. Around 7 months I found her at the same place and had to take her myself to have her Euthanised. I was so hard because I loved her too and my husband couldn't come. Her name was Alphie
My cousins gay but a really great guy and everyone knows him because he is. I love him myself and am proud of him
My mother had colon cancer and a lot of my other relatives died of this disease
Have had this since my late teens. When I was in 6th grade was in the hospital for 2 weeks because of nausea and throwing up - never found anything wrong.
Had this since I was young when I had big hard stools which caused it. Found out that I had a slow small intestine and back when I was little no one noticed what was going on.
Started with GERD and found out about 10 years ago. Feels like a heart attack when full blown. Everyone that listens to my heart beat hears the hernia also
Have this from MS, Fybro, OA, Addison's
Lots of gas and bloating cause was my Colon was dying or not funtioning anymore
I have been drinking milk all my life until I got lots of gas and alot of discomfort
I have been on SSDI for 24 years and would be at poverty level if it wasn't for an allowance from my husband who is in a nursing home. Got it fast but I went on it in 1990
WAs having horrible headaches. Neuro Doc did spinal tap and came back with this. Got rid of it but continued with the migraines.
I am 52 years old and about 4 years ago I got hot and sweaty in places that I didn't before. I was hot all the time. Now I haven't had my period for 5 months and feel cool air again.
I started getting Migraines when I was in my early 20's. I love throwing up and if anyone believes that one I'll tell you another one.
I have heart murmurs and two small leakages from too many high fevers
They found this in my late teens. I might have had it when I was 6. I blew up and mhy pants that fit the day before didn't fit the next day. They scoped me and found one the size of a dime.
I think this was passed down from an aunt to me.
After landing on the trampoline in high school twisted and tearing out all my muscles and ligaments I had this problem many times
My bladder completely gave up functioning from the MS and I use a foley catheter for the last 15 years.