cataracts

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Has anyone experienced a serious side effects from a medication?

Going for Catract surgery in 4 days caused from taking a very strong medication for just 6 months.
#Sarcoidosis ,#Cataracts ,#Pain ,
#side Effects, #chronic Pain,
#eye Surgery

2 people are talking about this
Community Voices

How do you keep your household going with multiple illnesses and only 1 other member in the house?

If I rest nothing runs smooth and if I don't rest, I run out of energy or the nerve pain gets too intense.
#chronic pain, # multiple health challenges #Pain , #home , #Sarcoidosis , #Cataracts

13 people are talking about this
Community Voices

Decisions, Decisions.

It's been awhile since I've posted on the Mighty. Still waiting for true dx on my spine. Have had more tests then I care to post. Angry at Drs. changing their minds every month while I get worse. Walking is difficult (meaning I have a 2 hrs window) can't bend over, or lift things. Can't feel my parts of my legs or feet. The pain is much worse. Dr who did injection test slipped and said I had a bulging disk on L4/5 and the surgeon told him spinal fusion?
News to me. So today, should I clean my house, or work on my painting project (of my cat that passed in 2019). I'm going to try to do both in that order but sometimes I just can't. I live alone so I need to do it all. Finances are low need to save for boarding cats if I have surgery. I'm so numb ' 2yrs. of this back and forth" I'm hoping for a dx in August from Neurosurgeon.
#ADHD
#Anxiety
#baastrupt SYNDROME
# BULDGING DISKS
#Cataracts
#Costochondritis
#Chondromalacia PATELLA L
#Fibromyalgia
# GERD
# HIVES ANGIOEDEMA IDOPATHIC #HIATIAL HERNIA
#Osteoporosis
# OSTEOPENIA
# PERPHIAL NEUROPATHY
#PLURISY W/D
# REYNARDS SYNDROME
# SHINGLES
#spinal STENOSIS
#unstable LUMBAR SPINE

5 people are talking about this
Community Voices

When the Other Shoe Drops
Use the Damn It Doll.

<p>When the Other Shoe Drops<br>Use the Damn It Doll.<br></p>
14 people are talking about this

Crohn's Disease: Life Lessons I Learned After Surgery to Remove Colon

I have Crohn’s disease. It has been in remission for 12 years, but from a year after my diagnosis in 1998 to August 2002, it was like a wildfire wreaking havoc on my body. I spent three years, from the summer of 1999 after my second son was born until my major surgery in 2002, fighting for my life. I didn’t realize it at the time. It snuck up on me in little increments, and before I knew it it had overtaken my body. Specifically, my large intestine. I was on a severely restricted diet and took handfuls of medication and vitamins. I was constantly in doctor’s offices or emergency rooms. I had raging fevers, higher than you would think a person could survive. Higher than the kind that send parents into panics. It hit 106 degrees. I had a racing heart even at rest, had steroid-induced cataracts, lost partial vision in my eyes from loss of blood flow to my optic nerve, and fought a staph infection in my leg for a week in the hospital. I never had the stomach pains that many people with Crohn’s do, but I probably spent more time in the bathroom than the average person will spend in their lives. My weight went down to 88 pounds. I fought having the surgery to remove my colon for a long time. I was too young to have an ostomy bag. I was only in my early 30s. How could I deal with that for my entire life? I finally gave in to myself — it was my choice. I wanted to be there for my boys, and I was just too ill to be the mom I wanted to be. When the surgeon went in for my pre-op colonoscopy, he couldn’t even complete it due to the swelling. I had put the procedure off, and if it had been done sooner I’m sure they would have told me how dire the circumstances were, but I’m glad I made the decision myself. I’m glad I did it for the love of my family. In the end, it would turn out to be so much more than that. That surgery saved my life. Literally. It was that bad. I can now eat anything I want, I take no medication for Crohn’s, and am back to a more-than-healthy weight. And I am living. Living a life I wouldn’t be, if not for said surgery. I am living a life I would not be, if not for Crohn’s disease. I have learned to appreciate the little things that so many take for granted. The blue sky, white clouds, green trees. The contrast between them, and the beauty of it. The breeze. The birds. The smell of fresh air. I have learned not to take my family and friends for granted, and to catch myself when I think that I am. To take care of them, as they took care of me. To love them with everything I have. To look to them for strength when I need it, and to give strength and support to them when they do. I have traveled farther out of my comfort zone than I ever thought I would. If not for Crohn’s we would not have traveled abroad, adopted our daughter or lived in China. Before Crohn’s my life was ruled by fear of the unknown — after Crohn’s, by the spirit of adventure and a love of life. The Great Wall of China, visited by Livy. I have walked on the Great Wall of China, and stood before the first emperor’s Terracotta Army. I have trekked through the rainforest in Langkawi, Malaysia, and floated through the mangroves. I have basked in the hope of longevity from the waterfall of the Pure Water Temple in Kyoto, Japan, and walked the nightingale floors of Nijo Castle. I have explored the streets of Ho Chi Minh City and traveled through the Mekong Delta. I have walked the beautiful beaches of Vietnam. I have zip-lined through the trees in Thailand and fed an elephant bananas — right into that giant mouth. I have been to the Demilitarized Zone in South Korea, and I have stood in North Korea, in the Military Armistice Commission building. Through my Crohn’s disease I learned how to live. How to love. How to learn. But I’m not done. I have so much more to see, so much more to experience, so much more to love, thanks to my Crohn’s disease. The Mighty is asking the following: What’s one thing people might not know about your experience with disability, disease or mental illness, and what would you say to teach them? If you’d like to participate, please send a blog post to community@themighty.com. Please include a photo for the piece, a photo of yourself and 1-2 sentence bio. Check out our Submit a Story page for more about our submission guidelines.