Laura’s Story

i am currently 26 with SLE Lupus, liver disease, asthma, major back problems seizures, auto immune disease, unable to walk or stand. wheelchair bound severe nerve pain and numbness and tingling that get’s worse everyday. severe back pain my body starts shaking out of no where. i took cipro a few times for UTI but didn’t have any severe symptoms till the last time 2015. i had surgery ended up having a UTI gave me cipro after having to come back from an allergic reaction to percocet and morphine caused me to have seizures again after being seizure free for 10 years. i couldn’t stay awake and don’t remember much except what my family said that they gave me cipro through IV very high dose. i was hallucinating really bad having excruciating pain in my legs and bleeding it wasn’t my period either i took it till i got out then i stopped it cause it was to much. about a month later the pain in my stomach returned and i started losing feeling with sex and started having more pain every day. i was in so much pain i couldn’t work and the seizures started getting to the point they were every minute or less and i would have a long where i wouldn’t be able to talk and lose all my strength and energy that happened 5 times in in 2015.

my memory was going on me i felt so sick all the time didn’t want to eat sometimes. then i found out i had sever fatty liver disease 84% fat that was september 2016 and my gall bladder was severely diseased and had to come out. i was very sick after i got it removed and a month after i started having bladder problems where i couldn’t control my bladder and going all the time and starting having pain again in my stomach not as bad but some pain. may 2017 i was working at out of no where i got exhausted and couldn’t stay awake i finished my shift but barely able to stay awake or walk my husband had to help me to the car. next day i was extremely slow slower then a snail barely able to move and no energy. and then i couldn’t walk i went to sleep and went in a coma for a day and a half i couldn’t wake up i could hear off and on but couldn’t wake up. then i started having breathing problems while i was in the coma and started choking and shaking really bad and thought i was going to die i couldn’t catch my breath. i woke up ate a little something then went into another coma for almost 3 days and it was harder to wake from my whole body was shaking i couldn’t stay awake. since may i still haven’t got my energy back i’m exhausted and been in a wheelchair june i found out i have Auto immune disease july i found out Sle lupus.

August i started losing feeling in my feet and became tingly then my legs and worked up to my arms and hands and face. august 26th i was unable to move at all i started choking and not being able to breathe my whole body started shaking and my whole body became paralyzed i couldn’t move anything not even my mouth i couldn’t talk i was drooling and couldn’t stay awake. my entire body has been numb since until a few days ago where i started having nerve pain all the time feels like electricity is being run through me from my back , finger tips, arms, hands, legs, ankles and toes it’s to the point where i am starting to have to take pain medicine cause of how much pain i’m in. i am currently in rehab right now trying to get strength back so i can walk again i’m very weak and this pain is making it really hard. i also feel like an old person and wake up every day wondering what obstacles i’m going to face each day and will i wake up I hope your feeling better and get better my friend told me about this i never realized but it makes sense now.

Michelle’s Story – Cipro Induced Lupus

Michelle Lupus

The diagnostic paperwork says, “Lupus – onset 3yrs ago: Triggered by Cipro use.”

 

Michelle’s story:

July 21st.2011 a day I will never forget. The day that I had my severe adverse reaction to Cipro.  The day prior I had went to my Dr.’s office because I felt the onset of a UTI, my children were in town and I didn’t want to be laid up in pain.

The Dr. asked me if I had taken Cipro before, I said “no.”

She then said to me really fast “If you feel pain in your arms let us know”. Then headed out to see the next patient.  I took 3 pills.. a dose and a half. An hour or so after my last pill I took I was so weak to lift my finger felt heavy.  My body ached everywhere. I then became so tired … It took my husband about 10 minutes to wake me up..to even get a reaction out of me.

Ever since then I have experienced heart racing, seizure, temporary hearing loss, stinging, burning, tingling, and numbing in my arms, legs, wrists ankles fingers shoulders…everywhere.  I have been up for hours at night crying in so much pain everywhere I just wanted to die.  So weak, exhausted. I have had loud ringing in my ears, my blood pressure has elevated to 140/100. I have never had high blood pressure. I am losing about 3 pouds a week. I have a huge loss of appetite.

I feel as though acid is running thru my veins and my body is burning inside.

These are just some of the things I have experienced , certainly not all.

Prior to Cipro I was active, loved to laugh, loved to go on walks. I smiled all the time. Now I am lucky if I can walk down 3 aisles at the store without stopping. It takes so much energy just to laugh.

Cipro has robbed me of me. Sucked everything out of me.

I didnt want my kids to have to deal with me in any kind of pain while they were here, I was doing the right thing by seeing the Dr.

What they ended up seeing was me in devistating pain, tears that will not stop and wondering if I was going to make it.

The Dr. didnt try anything else prior to giving me Cipro, didnt tell me that it had huge risks.. didnt even give me the option to choose.

I am forever scared of Dr.’s and they’re intent from now on.. never will I trust them.

I have told everyone I know to never take this , Those closest to me have seen the devistating effects of Cipro. For I have felt pain where I never knew pain existed..

My life has done a complete change.. the life I once had is gone. The mental anguish this has given me is beyond words..

everyday something new..the pain never stops.

Note – Three years after Michelle took Cipro she was diagnosed with Lupus.  Her paperwork stating that Lupus was brought on by Cipro is pictured above.