Physical therapy symptoms and conditions

I am wondering if the plantar foot pain that my husband is suffering for 6 months could be from lipitor that he is taking for several years now. Has anyone have this problem?

Hi, my name’s M. and I posted my story on here about a month ago. Unfortunately, I’ve made no progress. I was hospitalized again mid-October for numbness and tingling sensations in my legs, which is a symptom of guillian-barre syndrome and supposedly needs to be treated very carefully. I had an mri of my brain again, this time including my spine to check for possible tumors. I was sent home the next day, negative for guillian-barre, but having received no answers. I was crawling up the stairs by this time, and was too weak to walk without holding on to furniture to support myself. My legs felt like cement blocks, and the neurologist specifically said, “I don’t know why you can’t walk.”
Since then, I’ve developed acute mononucleosis, which increases my fatigue and muscle pain, and causes me to sleep about 15 hours a day. Recent blood work also showed I was positive for an autoimmune disorder called Myositis, which is a painful disorder that causes the body’s immune system to attack its muscles and connective tissue. I was referred to a rheumatologist, who was the least sympathetic person I’ve met in my life, and told me my physical exam was perfect, so she felt the Myositis must have been a false positive. She re-ran the blood work, and the Myositis was negative. This is of course a relief, but how we’ll ever know which test is correct, I don’t know. The rheumatologist did notice the weakness in my legs and my difficulty walking, and suggested physical therapy to help gain my strength back. She also prescribed an anti-inflammatory medication that took away almost all of my pain. Thank God, something finally worked for me. We then saw the physical therapist who said, “We can probably make you stronger, but I’ve never seen anything like this before.”
I’m seeing an osteopathic specialist who is convinced my illness is directly related to Gardasil. Through ancient medicine methods, she introduced a vile of Gardasil to my system and noticed an immediate weakness. I’m not sure if I totally believe in her practice, but the fact that she noticed a rejection to Gardasil the minute she introduced it is enough to convince me. She believes that my immune system was basically poisoned by the vaccine, which is causing it to fight off things I need. She also said it probably doesn’t recognize the mono as an infection, and decides not to fight it. For a normal, healthy person, mono can last up to 3 months. For someone like me, no one knows how long it could last. It was my immune system’s weakness that allowed me to develop mono, and it was the Gardasil that weakened it in the first place. So thank you Merck, for yet another thing I have to deal with.
And that brings us to today. I’ve missed about 30 days of my freshman year, so I’m assuming summer school will be necessary. My high school won’t provide a tutor, so I can only take my core curriculum classes, and am having difficulty keeping up with just those few. I’ve gained some strength in my legs, and it’s a little easier to walk with the anti-inflammatory, but I still can’t walk very far without resting. I’m also taking an anti-depressant to help me focus-hopefully it’ll lift my spirits. Since I received the vaccine, my periods have been painful and irregular. The constant nausea, headaches, and occasional stomach pain/joint pain continues, along with extreme fatigue.
The doctors make me feel like a crazy person who faked this to get out of school. How could I possibly fake nausea for thirteen weeks straight, and pain that kept me up crying almost every night? How could I fake my difficulty walking while it’s causing me to miss both of my volleyball seasons? Before this, I had hardly missed a day of school in my life, and refused to stay home whenever I got the flu because I hate falling behind. I’ve played volleyball tournaments with sprained ankles and chipped elbows, I can handle pain, and I’m not a baby. If the doctors would take five minutes out of their time to try to get to know me, maybe they would see that. And the few who actually take the time to be pleasant don’t listen. They tell you they know, that they understand, but they don’t. They won’t drag themselves out of bed in the morning feeling nauseous and half asleep; they’ll be able to walk into their office without feeling like they want to collapse, and they’ll go home to the people who care about them and will actually be awake long enough to enjoy their company. No one will tell them they’re insane, and the worst part is that most of them won’t take the time to realize how blessed they are just to have the ability to do those things. How can the doctors not have sympathy when they’re the ones who put this poison inside of me?!
I know I’m very lucky compared to girls who have experienced more serious side effects, and am thankful that we were able to make a connection between my illness and Gardasil after the first shot. But I’m living proof of what just one stupid shot can do to you-how can you put yourselves or your daughters at risk of what I’ve gone through? The benefits are not just worth the risk..
My 15th birthday is coming up in just a few weeks, and all I want is to be normal again.

My daughter is no longer on advair, but when she was I thought she was a hypochondriac. She had asthma since age 3 and by the time she was in 4th grade she was put on advair. She gained weight in her face and stomach. She would have trouble concentrating on her school work, stayed moody. She would lash out for little or no reason. She always had some ache or pain. Almost every day either her head hurt or her stomach hurt. It was would last under an hour each time

She started having muscle pains. had to be in a walking cast twice for soft tissue damage to her ankle. She would have no idea how it got hurt. If she crawled on her knees playing she would get fluid on her knees. She would have knee pain off and on for a weeks at a time. All the time we were at one doctor or another. Every one of them said her asthma medicine would not cause this. The last straw was when in 6th grade her shoulders would pop out of place if she tried to do push ups in gym. She had to have physical therapy three times a week for three months. Even though the doctors told me not to she has been off of advair for 4 years now. All of the side effects went away with the except for the problems with her shoulders. She has to do exercises a few time a week to keep the muscle's strong to hold them in place.

AVELOX should be banned from use. I took it last spring for a sinus infection. After only three days it damaged the tendons in my feet and calves so bad I can hardly walk. Now I'm in physical therapy twice a week and doctors won't believe that AVELOX did the damage even though it warns about it on the prescription instructions.

I'm very frustrated, still in pain, and it has cost me hundreds of dollars in bills since then.

Whatever you do, don't take Avelox!!!

I was given Avelox July 2007 .. within a week started getting severe leg pain in both legs .. making walking too difficult and painful... This pain has stayed with me 24/7 since I took the avelox over a year ago.. I have been to over 12 Doctors this past year trying to get help...and spent a small fortune with many tests done..now diagnosed with fibromyagia, osteoarthritis, cardioapathy, torn knee meniscus, adrenal fatigue, and i.b.s. which all developed after given Avelox... Not one will acknowledge that I may be suffering from a severe reaction to Avelox ... though they have no answers and have not been able to help me.. I have tried acupuncture, massage therapy, physical therapy, and steroid injections.. nothing has helped.. I am now seeing a Holistic Dr. and being treated for many hormone vitamin, and mineral deficiencies .. .I It has been a nightmare year with this 24/7 pain.. homebound.. because too painful to walk..and I also have constant gastric discomfort and insomnia. I feel my body has suffered from a very toxic reaction to the Avelox and just want to warn others out there too.... Please think twice before taking any antibiotics from the quinolone family...There are less toxic antibiotics that can be given.. not worth taking the risk of suffering serious reactions from these very poisonous antibiotics..

I am a 33 year old mother of 2 and i just been diagnosed with disk protrusion from L5-S1. as i worked for an ortho froup my doctor advised me to get an Epidural injecting which has relieved a lot of my pain especially in my legs and feet. unfortunately 2 days after receiving the injection i have started a menstrual that has now lasted 14 days ( i just finished my cycle a week prior from getting the injection). im also experiencing anxiety attacks whereas i cannot sleep at night. My husband and i are considering having another child and this whole situation is very frustrating. Im going to physical therapy 2-3 time a week for 3 weeks and i hope it will be of some help. My surgeon doesn't feel i should have back surgery he states im to young...help!!!!!

My daughter went for her yearly physical with our pediatrician. That morning we went in and the doctor insisted that she get immunized. Of course that immunization was Gardasil. My daughter felt fine and she was okay that day. After the doctors appointment she went on to school, and I went on to work to complete what I thought was to be a normal day. That afternoon I picked her up from school and she told me that she thought she may be getting sick. She complained of a stomach ache, and a mild headache. We went home and she ate very little, but told me and her dad that she felt better.
That evening she was to cheer at her first football game of the season in a neighboring town. She left with her best friend and her mother around 6 pm. at 8:44 that night her best friends mom called and told us that she had passed out at the game.
By the time that we had gotten there EMT's had taken her to the local ER, at that time she had barely regained consciousness, and her temperature was 103 degrees. Her extremities were cold, and her body was burning up. Her breathing was shallow, fast and irradic. Her pulse and blood pressure was extremely high. About an hour later the convulsions started.
After what seemed like eternity, the physician narrowed this down to the side effects of Gardasil. They started IV fluids, and meds, but still to no avail she kept convulsing. After a few days of heavily sedated sleep, she awoke to blurred vision, fever and nausea.
We were not told of any adverse reactions to this drug or we would have never given it to her!

I have muscle pain, weakness, and chronic lower back pain. Started statin drug, Simvastatin, on 11/21/07. I take no other drugs. Within two weeks, I could not sit without severe lower back pain. Reported problem to family medical doctor on 1/11/08. M.D. sent me to physical therapy for 8 sessions. No relief from physical therapy so I requested an X-ray on 3/20/08. X-ray shows very mild degeneration at one lower vertebrae. M.D. sent me to an orthopaedics doctor who recommended continued physical therapy. Went to a Chiropractor instead. After six chiropractic sessions with little relief, I made an appointment with an Osteopathic doctor. My M.D. sent me to a rheumatologist who prescribed high dose naproxen for two weeks. The rheumatologist ordered and X-ray of my lower back area. The lower back X-ray produced no negatives. The rheumatologist's next step will be to order and MRI of my lower back area. The D.O. suspects statin induced myopathy and because of hyper reflexes he ordered an MRI of my brain and cervical spine. I am now recommended to a neurologist who specializes in the diagnosis of multiple sclerosis. Am I getting the run around? Only one doctor said I might have statin induced myopathy. The rest will not even mention the statin drug theory. I just pray for ache and pain relief. I have some improvement after four months off of the statin which I believe is quite a strong point that it was the statin drug and not some unknown condition. I don't think arthritis or MS conditions improve. All I know is that I had no health issues before taking the simvastatin. Good luck to everyone who has or is taking a statin drug. BEWARE!!!

Hi

I just started taking 20mg of Prednisone for a shoulder injury. So far I have all but loss my appetite, which sounds strange to me since my doctor told me to expect to gain weight very quickly. I have also loss my need to sleep. I was up from Saturday 11:15 am morning the first day I began Prednisone and wasn't able to get to sleep until Sunday night around 10:00pm. I'm sweating like I'm constantly being rained on, it is so darn annoying. I also started to lose my voice last night and then again today, is that normal with is drug? I'm so full of energy all I do is clean our house, work out in my flower beds, etc. I'm kinda of scare of this drug and I'm glad I will be off of it next Tuesday unless my shoulder isn't better when I start physical therapy tomorrow. I wish you all the best while you are taking this drug.

Keep us posted on how you are doing.

Marlene

I was prescribed Levaquin by my Dr. for a sinus infection. There were 10 pills and I was to take one a day. No one mentioned any of the side effects or drug interactions except to not take antacids within 2 hours of taking the meds. During the coarse of me taking the medication I began having substernal chest pains which I thought was just horrible heart burn, but it got so bad that I woke up screaming multiple nights from the pain. I also started having pain in my ankles, legs and especially my knees. The pain in my knees gets so bad that I think my knee caps are going to shatter when I walk especially when going down the stairs. I didn't know any of the drug interactions and my father in law who is a physical therapist has always advised me to take ibuprofen for muscle and joint pain so that's what I did, but little did I know that was only increasing the effects on my central nervous system. I am also experiencing bouts of nausea, confusion, light headedness, difficulty sleeping, anxiety and I actually thought I was having a mental breakdown.. I was freaking out on my husband and very depressed even having suicidal thoughts. It wasn't until my mother randomly mentioned that she had heard about the FDA issuing the Black Box warning that I connected the dots and had already finished the meds. I called my doctor's office right away and was told that the symptoms I am having are not side effects of the medicine. Maybe the Dr. doesn't listen to the news either.

I have just finished taking Levaquin for a 10day treatment for pneumonia. In the last 5 days or so I have noticed stiffness in my achilles tendon (no pain) until I get moving. I have also notice a tremor in my hands and no muscle weakness and shaking in my triceps and quads. Of course I hadn't read the precautions to this drug before noticing these symptoms. I contacted both my pharmacist and physician and neither seemed concerned and told me if I was really worried to go to the emergency room. I am wondering if these symptoms will disappear since I am no longer on the drug, how long it will take, and how long I should worry about tendon damage----is the possibility of rupture forever???

Hi all, I was amazed to find this site. I too have had a rough life for the past eight years! I am going to be 39 in a few days but this story starts back in August 21, 2000. The day that put me in HELL for the next eight years and still going through it. Prior to this day, I had a lot of UTI's and Pneumonia and several times prescribed both Levaquin and Cipro. I did develop Achillies tendinitis but I thought this was due to my active life style, see I was an LPN and a firefighter. So I went for treatment to fix the Achillies tendinitis. This was a foot Dr that of course gave me a cortizone shot in it. I cant remember how much earlier this was that this took place and I am still not sure if this is what did it but as I am thinking back these are the things that come to mind. On August 21, 2000 I was on a fire call and my right Achillies tendon popped off the bone! They took me away by ambulance. The Dr in the ER said to go home with an air cast on, eat or drink nothing and come back in at 10:00am and they would possibly do surgery. Well, I did just that. The orthopedic Doc said oh yeah it is achillies rupture will have to go in and tie back all the little fibers. So away to the operating room I went. They gave me a spinal and just knocked me out. I was awakened suddenly by my Dr. voice loudly saying " Holy shit it peeled off the bone!" And another nurse saying let me see! I came up on my hands and they grabbed me put me back down and knocked me back out! (I still have night mares over that!) Anyway, I spent the next 3 months in a cast. During this time, I was told from over usuage of my left foot, I now was developing tendinitis in my achillies tendon in the left foot! Which this sent me to a wheel chair. They took the cast off in 3 months then I was still no weight bearing for another month. Then i had physical therapy for about 6-8 months with little improvement. I complained to the Dr about the left achillies tendon and he said he would not do anything about it unless it too popped! So now many Dr later, and many many medications tried and many surgeries later, and now diagnosed with Lupus, Sjogrens, and Fibromyalgia, the most my rheumatoligist says is I have a connective tissue disorder, and taking cancer medication (Methotrexate) I am now disabled at 39! My life taken from me. I have situational depression, panic attacks, sleep trouble, Suffer from post traumatic stress, nightmares, basically my life is a mess and it is over. On July 1, 2008 I had to go to the ER cause I was sick. I had been run down and feeling bad and sleeping a lot, disoriented, couldn't stay awake. They found I had another UTI and a sinus infection. The Dr Says we will put you on Levaquin and that should take care of both problems. So he left, it took me a while for it to sink in that I should stay away from that drug, so I caught him and told him, he said to me that this was only found to be in kids while they are young and developing that it causes tendon rupture, and besides he said, one dose will not hurt you. I took 5 pills, one a day. Since then I have been in so much pain all over my body it is unreal! It still took me days to figure out that it was the Levaquin doing this to me! I feel like at random someone is sticking a knife in different muscles in my body! I felt like I had done Tie bo for 24 hours straight! Even my butt muscles hurt so bad to sit here and write this email! I have days when I cant even use my hands! Write my name with a pen. I am not sure if this is all due to these drugs, but I am most miserable and not a bit better. I may have just made it worse by taking this last round of them. Has anyone else had this kinf of symptoms?

I took Cipro many times but in November I took it with a prednisone dose pack, this seems to make the tendon issue worse according to todays report.

I have had severe achiles tendon pain for 7 months now. I can't bend my ankle when I walk. I also had surgery for a torn rotator cuff in December, no injury to my shoulder, it just tore.

I have wide spread tendinitis an now I know why. Is this a temporary situation? I hope!!!
ksquared

In response to Wewe's post, I've been wondering the same thing. Since taking my daughter off Singular almost 2 months ago, I'm seeing a different almost typical kid. Four years ago about 2 months after starting Singular my daughter was diagnosed with anxiety. As her condition got worse she was diagnosed with depression. We started to see OCD and tics so they were added as a diagnosis It was determined that it was related to strep infections so she was diagnosed with PANDAS. She was started on Zoloft and klonidine. The Zoloft made her worse. Her fears of hurting herself got so intrusive she was hospitalized. Her cholesterol was high too. The Zoloft was discontinued and Prozac was started. She's had therapy all 4 years. She also neede physical therapy due to muscle and joint pain. Now she's doing better, off Singular. Does she really have PANDAS, OCD? I don't know. She's still on Prozac, we just did a slight decrease this week. Is this medication the trigger for underlying conditions. Learned behaviors can be unlearned, but are there lasting physical effects? If a gene has been turned on, can it be turned off? I wish we knew the answers to help all of our kids.

My jaw dropped after reading all of these posts. I started on Yasmin 3 weeks ago. I've never really been on BC's before, so I thought that my headaches, numbness and fatigue were just because of school. I finally connected the dots and looked on the internet to see if it was the Yasmin or if i was just crazy. I am so thankful to have found this website. I wish it was in the paper or advertised. Doctors should not even be able to prescribe this drug.

I have been on lyrica for over a year for the treatment of RSD (Reflex Sympathetic Dystrophy). The biggest side effect that I have had has been weight gain. I have gained approx. 55lbs since I was first diagnosed 3 years ago-- At least 30 of those have been in the last year from the lyrica. No matter how healthy I eat, or how much physical therapy I do I still can not seem to shed the pounds

After approximately six months of Vivelle-Dot - .05 mg experienced increasingly severe back, calf, ankle and foot pain to the point where I could barely walk or stand. Vivelle-Dot only medication.
• Numerous orthopedic appointments for back and feet;
• X-rays;
• MRIs
• Treated for Achilles tendinitis;
• wore light boot at night for several weeks;
• wore lydocaine patches;
• wore heavy boot during the day for six weeks;
• Physical Therapy;
• PAIN, pain and more pain

Researched Vivelle-Dot on internet. GYN suggested going off patch for a month. Stopped using Novartis VIVELLE-DOT (.05 mg) patches (Estradiol transdermal system) May 11, 2008. All symptoms related to my legs vanished within several days.

Trying to figure out if my back pain is like others. The pain is in the lower left side and groin area of both hips. I have trouble reaching my feet to put on shoes and socks. Ive been on Lipitor 20 for about 5 years and have never had a problem before. This started about 6 months ago and even with heat and stretching it seems to get worse. It hurts when I stand for any length of time. It hurts to walk or run. It hurts very badly if I try to straddle something like an ATV or a horse. When I sleep (if I can) I sometimes have to put a pillow between my legs and lay on my side because it hurts a lot to bring my legs together. Feel free to email me at ******

I'm a 46 years old male normally good shape,I was put on Lipitor due to high cholesterol and family history of heart problems.I've been on lipitor for four years , 2years on 10mg, 1 years on 40mg and 1 year on 80 mg.
The last 6 months I have been experiencing severe archiles tendonitis to the point where I can hardly walk. I am extremely disatisfied with this drug and have read a lot of complaints regarding this drug.

Has anyone else experienced this side effect?

Please reply to this post.

Thank You

I am so relieved to come across this forum. I have been on Yasmin for about 3 years. After reading several postings here to my husband, we were both horrified to hear that I wasn't the only one having strange issues without a clear cause. I too have had heart palpitations, anxiety attacks, uncontrollable mood swings, inability to concentrate at work or deal with normal work stress, back pain, trouble falling asleep, low sex drive, and most recently, horrible depression. I have been to psychiatrists, allergists, chiropractors and physical therapy - all to try to find the cause. I have just gone off the pill, and have noticed improvement so far, and am very excited to see it hopefully improve. Hopefully I will be able to find a hormone-free birth control, instead of dealing with this. I can't believe doctors do not discuss these possible symptoms with their patients. I never would have thought bc pills would cause anxiety, depression, etc. A huge thanks to all of you for your candid comments... and helping me find an answer to my life-altering side affects!!!

I quit Lipitor (40mg) five weeks ago. I believe I was on a trajectory to disabilty within a year.
The unbelievable left elbow pain has gone (maybe the cortisone worked!). My left knee feels "normal" again, not perfect but nearly like it used to be. Within a couple of days of quitting I had severe pain in my right thumb along the bone, then in the middle of my right hand, then between the first and second fingers in my right hand. I currently have minor pain in my right wrist (this is new) on the pinkie side and minor pain in my left shoulder where the arm joins (this has been intermittent for a couple of months). I am feeling much better - but would not be at all surprised if pain appears in another part of my body before this is all history! There is also plenty of joint clicking going on.
I believe I first reported pain to the assistant doctor to the heart surgeon two weeks after I had the stent put in and was put on Lipitor. I was also on various other medications. I had tingling on the ends of my fingers and toes at random - hard to describe but it was as if a fairly sharp object (like a ball point pen, say) was being pressed progressively harder from the end of the finger/toe and towards the rest of that finger/toe: and as the pressure increased it would suddenly become painful. It was not a tingling/numb sensation but more a tingling which increased sufficiently that it hurt.
I am only being so specific because when I described these "symptoms" the doctor shrugged. If anyone has had similar - and I have seen tingling mentioned here - please make contact with me as I do want to report my experience back into the medical community but find, an exact description difficult. Things never needed to have got so bad if this was the first warning.
I since asked my family doctor if my knee problem was Lipitor related and she thought not: I was referred to Physical Therapy. I also told the physical therapists (who thought my knee should recover much sooner, and were surprised that I had zero mobility pain) that I also had serious elbow pain.
The orthopedic surgeon I saw did not connect the elbow problem to Lipitor.
The heart surgeon (stent insert) could perhaps be the only person who I did not tell of the pains - I don't remember - but I may be so grateful to be alive - that he may be someone to whom I did not voice a complaint!
On the positive - five weeks later I am feeling significantly better.

I posted my experience with Levaquin back in January 2008. It's been three months since my initial reaction to Levaquin. I was in terrible pain then and I could barely walk. It has been three months now and I am still in a lot of pain and the pain in my lower back is worse. However, I can walk better now. I have yet to find a doctor who can help me or who even believes that Levaquin caused this. If anyone out there has a physician who believes that Levaquin can cause this damage and who is competent to treat this problem, PLEASE email me with his or her name. I am willing to travel to wherever I need to travel to to get some relief from this. If nothing else it would be great to have a doctor who understands the problem. Thanks. My prayers are with you all.

Chris

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona

I'm 17 and I took Levaquin back in November and still have to use a wheelchair to get around. I ended up having to go to the Mayo clinic because there were so many factors to my case, and we were not getting anywhere with my doctors at children's hospital. i also have mono and west nile virus and so all that viral activity made the reaction so much worse. They discovered Levaquin caused severe tendinitis in each and every tendon, but my hips mainly affected causing them to be extremely fluid-filled. I also have a permanent peripheral neuropathy from it. They discovered an autonomic syndrome called POTS (postural orthostatic tachycardia syndrome) , however that can logically be attributed to either the mono or the reaction.
I go to physical therapy every week now for my hips and my ability to be ambulating well enough to go to college in 6 months is being questioned.

I was on the way to work about 5 months ago and i was rear ended at a stop light. I was a little sore but since I work at a doctors office I signed in as soon as i got to work just to get an x ray of my chest from the seat belt. Thank Jesus I was fine but a a month later I was still having pain in my left shoulder blade. One day at work a provider there saw me rolling my shoulder around as if I was in pain, he offered me an injection repeatedly stating that it would sting for a few seconds and then I'd feel like a new woman. I put aside my EXTREME fear of needles to get the injection because I knew I still had several hours to work. After the injection my back never stopped hurting that night i just tossed and turned. People at work make fun of me because my chair sits almost completely forward but i try to tell them it is my back. well it is now 3 months later and 2 days ago i saw a different provider at my work for depression and anxiety problems. during the end of the visit i made a comment about my back after looking at it one time she had 3 other doctors in there with us all gasping at what they saw. My office manager promised to take care of all of my copays and deductible for plastic surgery and physical therapy to repair the crater in my shoulder blade. But is that enough? I mean to my knowledge they can make it LOOK better but I will always have pain and i can never regain that muscle back...its scary. I mean I'm only 21 years old! Any to all of you I have my "consultation" with my plastic surgeon on the 31st so i will keep you updated and let the ones of you that are curious if it is worth it or not. Thanks for listened.....